المؤلفون: McGrath, L.M., Yu, D. (D.), Marshall, C.R. (Christian), Davis, L.K. (Lea), Thiruvahindrapuram, B. (Bhooma), Li, B. (Bingbin), Cappi, C. (Carolina), Gerber, G. (Gloria), Wolf, A. (Anneke) de, Schroeder, F.A. (Frederick), Osiecki, L. (Lisa), O'Dushlaine, C. (Colm), Kirby, A. (Andrew), Illmann, C. (Cornelia), Haddad, S. (Stephen), Gallagher, P. (Patience), Fagerness, J. (Jesen), Barr, C.L. (Cathy), Bellodi, L. (Laura), Benarroch, F. (Fortu), Bienvenu, O.J. (Oscar), Black, D.W. (Donald), Bloch, J. (Jocelyne), Bruun, R.D. (Ruth), Budman, C.L. (Cathy), Camarena, B. (Beatriz), Cath, D. (Daniëlle), Cavallini, M.C. (Maria), Chouinard, S., Coric, V. (Vladimir), Cullen, C., Delorme, R. (Richard), Denys, D.A.J.P. (Damiaan), Derks, E.M. (Eske), Dion, Y. (Yves), Rosário, M.C. (Maria), Eapen, C.E. (Chundamannil Eapen), Evans, P., Falkai, P. (Peter), Fernandez, T.V. (Thomas), Garrido, H. (Helena), Geller, D. (Daniel), Grabe, H.J. (Hans Jörgen), Grados, M. (Marco), Greenberg, B.D. (Benjamin), Gross-Tsur, V. (Varda), Grünblatt, E. (Edna), Heiman, M.L. (Mark), Hemmings, S.M.J. (Sian), Herrera, L.D. (Luis), Hounie, A.G. (Ana), Jankovic, J. (Joseph), Kennedy, J.L., King, R.A., Kurlan, R., Lanzagorta, N. (Nuria), Leboyer, M. (Marion), Leckman, J.F., Lennertz, L. (Leonhard), Lochner, C. (Christine), Lowe, T.L. (Thomas), Lyon, H.N. (Helen), MacCiardi, F. (Fabio), Maier, W. (Wolfgang), McCracken, J.T. (James), McMahon, W.M. (William), Murphy, D.L. (Dennis), Naarden, A.L. (Allan), Nurmi, E. (Erika), Pakstis, A.J., Pato, C. (Carlos), Piacentini, J. (John), Pittenger, C. (Christopher), Pollak, M.N. (Michael), Reus, V.I. (Victor), Richter, M.A. (Margaret), Riddle, M. (Mark), Robertson, M.M., Rosenberg, D. (David), Rouleau, G.A., Ruhrmann, S. (Stephan), Sampaio, A.S. (Aline), Samuels, J. (Jonathan), Sandor, P. (Paul), Sheppard, B. (Brooke), Singer, H.S. (Harvey), Smit, J.H. (Jan), Stein, D.J. (Dan), Tischfield, J.A. (Jay), Vallada, H. (Homero), Veenstra-Vanderweele, J. (Jeremy), Walitza, S. (Susanne), Wang, Y. (Ying), Wendland, A. (Annika), Shugart, Y.Y., Miguel, E.C. (Euripedes), Nicolini, H. (Humberto), Oostra, B.A. (Ben), Moessner, R. (Rainald), Wagner, M. (Michael), Ruiz-Linares, A. (Andres), Heutink, P. (Peter), Nestadt, G. (Gerald), Freimer, N.B. (Nelson), Petryshen, T.L. (Tracey), Posthuma, D. (Danielle), Jenike, M.A. (Michael), Cox, N.J. (Nancy), Hanna, G.L. (Gregory), Brentani, H. (Helena), Scherer, S.W. (Stephen), Arnold, P.D. (Paul), Stewart, S.E., Mathews, C., Knowles, J.A. (James A), Cook, E.H. (Edwin), Pauls, D.L. (David), Wang, K. (Kai), Scharf, J.M., Neale, B.M. (Benjamin)

المصدر: American Academy of Child and Adolescent Psychiatry. Journal vol. 53 no. 8, pp. 910-919

مصطلحات موضوعية: 16p13.11, copy number variation, genetics, obsessive-compulsive disorder, Tourette syndrome

Relation: http://repub.eur.nl/pub/67630; urn:hdl:1765/67630

الاتاحة: http://repub.eur.nl/pub/67630
https://doi.org/10.1016/j.jaac.2014.04.022

المؤلفون: Davis, L.K., Yu, D., Keenan, C.L., Gamazon, E.R., Konkashbaev, A.I., Derks, E.M., Neale, B.M., Yang, J., Lee, S.H., Evans, P., Barr, C.L., Bellodi, L., Benarroch, F., Berrio, G.B., Bienvenu, O.J., Bloch, M.H., Blom, R.M., Bruun, R.D., Budman, C.L., Camarena, B., Campbell, D., Cappi, C., Cardona Silgado, J.C., Cath, D.C., Cavallini, M.C., Chavira, D.A., Chouinard, S., Conti, D.V., Cook, E.H., Coric, V., Cullen, B.A., Deforce, D., Delorme, R., Dion, Y., Edlund, C.K., Egberts, K., Falkai, P., Fernandez, T.V., Gallagher, P.J., Garrido, H., Geller, D., Girard, S.L., Grabe, H.J., Grados, M.A., Greenberg, B.D., Gross-Tsur, V., Haddad, S., Heiman, G.A., Hemmings, S.M., Hounie, A.G., Illmann, C., Jankovic, J., Jenike, M.A., Kennedy, J.L., King, R.A., Kremeyer, B., Kurlan, R., Lanzagorta, N., Leboyer, M., Leckman, J.F., Lennertz, L., Liu, C., Lochner, C., Lowe, T.L., Macciardi, F., McCracken, J.T., McGrath, L.M., Mesa Restrepo, S.C., Moessner, R., Morgan, J., Muller, H., Murphy, D.L., Naarden, A.L., Ochoa, W.C., Ophoff, R.A., Osiecki, L., Pakstis, A.J., Pato, M.T., Piacentini, J., Pittenger, C., Pollak, Y., Rauch, S.L., Renner, T.J., Reus, V.I., Richter, M.A., Riddle, M.A., Robertson, M.M., Romero, R., Rosàrio, M.C., Rosenberg, D., Rouleau, G.A., Ruhrmann, S., Ruiz-Linares, A., Sampaio, A.S., Samuels, J., Sandor, P., Sheppard, B., Singer, H.S., Smit, J.H., Stein, D.J., Strengman, E., Tischfield, J.A., Valencia Duarte, A.V., Vallada, H., van Nieuwerburgh, F., Veenstra-Vanderweele, J., Walitza, S., Wang, Y., Wendland, J.R., Westenberg, H.G., Shugart, Y.Y., Miguel, E.C., McMahon, W., Wagner, M., Nicolini, H., Posthuma, D., Hanna, G.L., Heutink, P., Denys, D., Arnold, P.D., Oostra, B.A., Nestadt, G., Freimer, N.B., Pauls, D.L., Wray, N.R., Stewart, S.E., Mathews, C.A., Knowles, J.A., Cox, N.J., Scharf, J.M.

المصدر: Davis , L K , Yu , D , Keenan , C L , Gamazon , E R , Konkashbaev , A I , Derks , E M , Neale , B M , Yang , J , Lee , S H , Evans , P , Barr , C L , Bellodi , L , Benarroch , F , Berrio , G B , Bienvenu , O J , Bloch , M H , Blom , R M , Bruun , R D , Budman , C L , Camarena , B , Campbell , D , Cappi ....

الاتاحة: https://research.vu.nl/en/publications/4bb3389d-810f-4b8c-9a12-9ad83d7f25cd
https://doi.org/10.1371/journal.pgen.1003864
https://hdl.handle.net/1871.1/4bb3389d-810f-4b8c-9a12-9ad83d7f25cd

المؤلفون: Maxwell, C.A., Benítez, J., Gómez-Baldó, L., Osorio, A., Bonifaci, N., Fernández-Ramires, R., Costes, S.V., Guinó, E., Chen, H., Evans, G.J.R., Mohan, P., Català, I., Petit, A., Aguilar, H., Villanueva, A., Aytes, A., Serra-Musach, J., Rennert, G., Lejbkowicz, F., Peterlongo, P., Manoukian, S., Peissel, B., Ripamonti, C.B., Bonanni, B., Viel, A., Allavena, A., Bernard, L., Radice, P., Friedman, E., Kaufman, B., Laitman, Y., Dubrovsky, M., Milgrom, R., Jakubowska, A., Cybulski, C., Gorski, B., Jaworska, K., Durda, K., Sukiennicki, G., Lubiński, J., Shugart, Y.Y., Domchek, S.M., Letrero, R., Weber, B.L., Hogervorst, F.B.L., Rookus, M.A., Collee, J.M., Devilee, P., Ligtenberg, M.J., van der Luijt, R.B., Aalfs, C.M., Waisfisz, Q., Wijnen, J., van Roozendaal, C.E.P., Easton, D.F., Peock, S., Cook, M., Oliver, C., Frost, D., Harrington, P., Evans, D.G., Lalloo, F., Eeles, R., Izatt, L., Chu, C., Eccles, D., Douglas, F., Brewer, C., Nevanlinna, H., Heikkinen, T., Couch, F.J., Lindor, N.M., Wang, X., Godwin, A.K., Caligo, M.A., Lombardi, G., Loman, N., Karlsson, P., Ehrencrona, H., von Wachenfeldt, A., Barkardottir, R.B., Hamann, U., Rashid, M.U., Lasa, A., Caldés, T., Andrés, R., Schmitt, M., Assmann, V., Stevens, K., Offit, K., Curado, J., Tilgner, H., Guigó, R., Aiza, G., Brunet, J., Castellsagué, J., Martrat, G., Urruticoechea, A., Blanco, I., Tihomirova, L., Goldgar, D.E., Buys, S., John, E.M., Miron, A., Southey, M., Daly, M.B., Schmutzler, R.K., Wappenschmidt, B., Meindl, A., Arnold, N., Deissler, H., Varon-Mateeva, R., Sutter, C., Niederacher, D., Imyamitov, E., Sinilnikova, O.M., Stoppa-Lyonne, D., Mazoyer, S., Verny-Pierre, C., Castera, L., de Pauw, A., Bignon, Y.J., Uhrhammer, N., Peyrat, J.P., Vennin, P., Fert-Ferrer, S., Collonge-Rame, M.A., Mortemousque, I., Spurdle, A.B., Beesley, J., Chen, X., Healey, S., Barcellos-Hoff, M.H., Vidal, M., Gruber, S.B., Lázaro, C., Capellá, G., McGuffog, L., Nathanson, K.L., Antoniou, A.C., Chenevix-Trench, G., Fleisch, M.C., Moreno, V., Pujana, M.A.

المصدر: Maxwell , C A , Benítez , J , Gómez-Baldó , L , Osorio , A , Bonifaci , N , Fernández-Ramires , R , Costes , S V , Guinó , E , Chen , H , Evans , G J R , Mohan , P , Català , I , Petit , A , Aguilar , H , Villanueva , A , Aytes , A , Serra-Musach , J , Rennert , G , Lejbkowicz , F , Peterlongo , P , Manoukian , S , Peissel , B , Ripamonti , C B , Bonanni , ....

وصف الملف: application/pdf

Relation: https://dare.uva.nl/personal/pure/en/publications/interplay-between-brca1-and-rhamm-regulates-epithelial-apicobasal-polarization-and-may-influence-risk-of-breast-cancer(0d984a4d-b6d9-4319-837d-4be05bc12eb4).html

الاتاحة: https://dare.uva.nl/personal/pure/en/publications/interplay-between-brca1-and-rhamm-regulates-epithelial-apicobasal-polarization-and-may-influence-risk-of-breast-cancer(0d984a4d-b6d9-4319-837d-4be05bc12eb4).html
https://doi.org/10.1371/journal.pbio.1001199
https://pure.uva.nl/ws/files/1183828/118201_364530.pdf

المؤلفون: Maxwell C.A., Benítez J., Gómez-Baldó L., Osorio A., Bonifaci N., Fernández-Ramires R., Costes S.V., Guinó E., Chen H., Evans G.J.R., Mohan P., Català I., Petit A., Aguilar H., Villanueva A., Aytes A., Serra-Musach J., Rennert G., Lejbkowicz F., Peterlongo P., Manoukian S., Peissel B., Ripamonti C.B., Bonanni B., Viel A., Allavena A., Bernard L., Radice P., Friedman E., Kaufman B., Laitman Y., Dubrovsky M., Milgrom R., Jakubowska A., Cybulski C., Gorski B., Jaworska K., Durda K., Sukiennicki G., Lubi?ski J., Shugart Y.Y., Domchek S.M., Letrero R., Weber B.L., Hogervorst F.B.L., Rookus M.A., Collee J.M., Devilee P., Ligtenberg M.J., van der Luijt R.B., Aalfs C.M., Waisfisz Q., Wijnen J., van Roozendaal C.E.P., HEBON Hereditary Breast and Ovarian Cancer Group, EMBRACE Centre for Cancer Genetic Epidemiology, Easton D.F., Peock S., Cook M., Oliver C., Frost D., Harrington P., Lalloo F., Eeles R., Izatt L., Chu C., Eccles D., Douglas F., Brewer C., Nevanlinna H., Heikkinen T., Couch F.J., Wang X., Lindor N.M., Godwin A.K., Caligo M.A., Lombardi G., Loman N., Karlsson P., Ehrencrona H., von Wachenfeldt A., SWE-BRCA Swedish Breast Cancer Study, Barkardottir R., Hamann U., Rashid M.U., Lasa A., Caldés T., Andrés R., Schmitt M., Assmann V., Stevens K., Offit K., Curado J., Tilgner H., Guigó R., Aiza G., Brunet J., Martrat G., Urruticoechea A., Blanco I., Tihomirova L., Goldgar D.E., Buys S., John E.M., Miron A., Southey M., Daly M.B., BCFR Breast Cancer Family Registry, Schmutzler R.K., Wappenschmidt B., Meindl A., Arnold N., Deissler H., Varon-Mateeva R., Sutter C., Niederacher D., Imyamitov E., Sinilnikova O.M., Stoppa-Lyonne D., Mazoyer S., Verny-Pierre C., Castera L., de Pauw A., Bignon Y.-J., Uhrhammer N., Peyrat J.-P., Vennin P., Ferrer S., Collonge-Rame M.-A., Mortemousque I., GEMO Study Collaborators GEMO Study, Spurdle A.B., Beesley J., Chen X., Healey S., Barcellos-Hoff M.H., Gruber S.B., Lázaro C., Capellá G., McGuffog L., Nathanson K.L., Chenevix-Trench G., Fleisch M.C., Moreno V., Pujana M.A.

المساهمون: DUKE-NUS MEDICAL SCHOOL

المصدر: Unpaywall 20191101

مصطلحات موضوعية: BRCA1 protein, BRCA2 protein, cell protein, estrogen receptor, nuclear protein, protein AURKA, protein RHAMM, protein TPX2, unclassified drug, aurora kinase, human, Hermes antigen, hyaluronan mediated motility receptor, hyaluronan-mediated motility receptor, protein serine threonine kinase, scleroprotein, article, breast cancer, breast carcinogenesis, cancer risk, cell polarity, controlled study, epithelial apicobasal polarization, gene locus, gene mutation, genetic analysis, genetic variability, human cell, microtubule, molecular interaction

Relation: Maxwell C.A., Benítez J., Gómez-Baldó L., Osorio A., Bonifaci N., Fernández-Ramires R., Costes S.V., Guinó E., Chen H., Evans G.J.R., Mohan P., Català I., Petit A., Aguilar H., Villanueva A., Aytes A., Serra-Musach J., Rennert G., Lejbkowicz F., Peterlongo P., Manoukian S., Peissel B., Ripamonti C.B., Bonanni B., Viel A., Allavena A., Bernard L., Radice P., Friedman E., Kaufman B., Laitman Y., Dubrovsky M., Milgrom R., Jakubowska A., Cybulski C., Gorski B., Jaworska K., Durda K., Sukiennicki G., Lubi?ski J., Shugart Y.Y., Domchek S.M., Letrero R., Weber B.L., Hogervorst F.B.L., Rookus M.A., Collee J.M., Devilee P., Ligtenberg M.J., van der Luijt R.B., Aalfs C.M., Waisfisz Q., Wijnen J., van Roozendaal C.E.P., HEBON Hereditary Breast and Ovarian Cancer Group, EMBRACE Centre for Cancer Genetic Epidemiology, Easton D.F., Peock S., Cook M., Oliver C., Frost D., Harrington P., Lalloo F., Eeles R., Izatt L., Chu C., Eccles D., Douglas F., Brewer C., Nevanlinna H., Heikkinen T., Couch F.J., Wang X., Lindor N.M., Godwin A.K., Caligo M.A., Lombardi G., Loman N., Karlsson P., Ehrencrona H., von Wachenfeldt A., SWE-BRCA Swedish Breast Cancer Study, Barkardottir R., Hamann U., Rashid M.U., Lasa A., Caldés T., Andrés R., Schmitt M., Assmann V., Stevens K., Offit K., Curado J., Tilgner H., Guigó R., Aiza G., Brunet J., Martrat G., Urruticoechea A., Blanco I., Tihomirova L., Goldgar D.E., Buys S., John E.M., Miron A., Southey M., Daly M.B., BCFR Breast Cancer Family Registry, Schmutzler R.K., Wappenschmidt B., Meindl A., Arnold N., Deissler H., Varon-Mateeva R., Sutter C., Niederacher D., Imyamitov E., Sinilnikova O.M., Sinilnikova O.M., Stoppa-Lyonne D., Mazoyer S., Verny-Pierre C., Castera L., de Pauw A., Bignon Y.-J., Uhrhammer N., Peyrat J.-P., Vennin P., Ferrer S., Collonge-Rame M.-A., Mortemousque I., GEMO Study Collaborators GEMO Study, Spurdle A.B., Beesley J., Chen X., Healey S., Barcellos-Hoff M.H., Barcellos-Hoff M.H., Gruber S.B., Lázaro C., Capellá G., McGuffog L., Nathanson K.L., Chenevix-Trench G., Fleisch M.C., Moreno V., Pujana M.A. (2011). Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer. PLoS Biology 9 (11) : e1001199. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pbio.1001199; https://scholarbank.nus.edu.sg/handle/10635/161649

الاتاحة: https://scholarbank.nus.edu.sg/handle/10635/161649

المؤلفون: Bienvenu, O.J., Wang, Y., Shugart, Y.Y., Welch, J.M., Grados, M.A., Fyer, A.J., Rauch, S.L., McCracken, J.T., Rasmussen, S.A., Murphy, D.L., Cullen, B., Valle, D., Hoehn‐Saric, R., Greenberg, B.D., Pinto, A., Knowles, J.A., Piacentini, J., Pauls, D.L., Liang, K.Y., Willour, V.L., Riddle, M., Samuels, J.F., Feng, G., Nestadt, G.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 150B, issue 5, page 710-720 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.30897
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.30897
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.30897

المؤلفون: Ferland, R.J, Eyaid, W, Collura, R.V, Tully, L.D, Hill, R.S, Al-Nouri, D, Al-Rumayyan, A, Topcu, M, Gascon, G, Bodell, A, Shugart, Y.Y, Ruvolo, M, Walsh, C.A.

المساهمون: Çocuk Sağlığı ve Hastalıkları

وصف الملف: text/plain; application/pdf

Relation: Nature Genetics; https://doi.org/10.1038/ng1419; https://www.scopus.com/inward/record.url?eid=2-s2.0-4444311117&partnerID=40&md5=b879e698f5727b903a91955f35261195; http://hdl.handle.net/11655/14250; 36; 1008; 1013

الاتاحة: http://hdl.handle.net/11655/14250
https://doi.org/10.1038/ng1419
https://www.scopus.com/inward/record.url?eid=2-s2.0-4444311117&partnerID=40&md5=b879e698f5727b903a91955f35261195

المؤلفون: Staratschek‐Jox, A., Shugart, Y.Y., Strom, S.S., Nagler, A., Taylor, G.M.

المصدر: Annals of Oncology ; volume 13, page 30-33 ; ISSN 0923-7534

الاتاحة: http://dx.doi.org/10.1093/annonc/13.s1.30
https://api.elsevier.com/content/article/PII:S0923753420312266?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0923753420312266?httpAccept=text/plain
http://academic.oup.com/annonc/article-pdf/13/suppl_1/30/524633/mdf604.pdf

المؤلفون: Nestadt, G., Lan, T., Samuels, J., Riddle, M., Bienvenu, O.J., Liang, K.Y., Hoehn-Saric, R., Cullen, B., Grados, M., Beaty, T.H., Shugart, Y.Y.

المصدر: The American Journal of Human Genetics ; volume 67, issue 6, page 1611-1616 ; ISSN 0002-9297

الاتاحة: http://dx.doi.org/10.1086/316898
https://api.elsevier.com/content/article/PII:S0002929707632339?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0002929707632339?httpAccept=text/plain

المؤلفون: Guo, W., Samuels, J.F., Wang, Y., Cao, H., Ritter, M., Nestadt, P.S., Krasnow, J., Greenberg, B.D., Fyer, A.J., McCracken, J.T., Geller, D.A., Murphy, D.L., Knowles, J.A., Grados, M.A., Riddle, M.A., Rasmussen, S.A., McLaughlin, N.C., Nurmi, E.L., Askland, K.D., Cullen, B.A., Piacentini, J., Pauls, D.L., Bienvenu, O.J., Stewart, S.E., Goes, F.S., Maher, B., Pulver, A.E., Valle, D., Mattheisen, M., Qian, J., Nestadt, G., Shugart, Y.Y.

المساهمون: IRP-NIMH-NIH, NIMH

المصدر: European Neuropsychopharmacology ; volume 27, issue 7, page 657-666 ; ISSN 0924-977X

الاتاحة: http://dx.doi.org/10.1016/j.euroneuro.2017.03.011
https://api.elsevier.com/content/article/PII:S0924977X17301931?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0924977X17301931?httpAccept=text/plain

المؤلفون: Stewart, S.E., Mayerfeld, C., Arnold, P.D., Crane, J.R., O'Dushlaine, C., Fagerness, J.A., Yu, D., Scharf, J.M., Chan, E., Kassam, F., Moya, P.R., Wendland, J.R., Delorme, R., Richter, M.A., Kennedy, J.L., Veenstra‐vanderweele, J., Samuels, J., Greenberg, B.D., McCracken, J.T., Knowles, J.A., Fyer, A.J., Rauch, S.L., Riddle, M.A., Grados, M.A., Bienvenu, O.J., Cullen, B., Wang, Y., Shugart, Y.Y., Piacentini, J., Rasmussen, S., Nestadt, G., Murphy, D.L., Jenike, M.A., Cook, E.H., Pauls, D.L., Hanna, G.L., Mathews, C.A.

المساهمون: Department of Psychiatry, University of Michigan, Ann Arbor, Michigan, Department of Child and Adolescent Psychiatry, AP‐HP, Robert Debré Hospital, INSERM U955, Paris, France, Institut Mondor de Recherche Biomédicale, Psychiatric Genetics, Créteil, France, Foundation Fondamental, French National Science Foundation, Paris, France, Department of Psychiatry, Clinic for OCD and Related Disorders, Sunnybrook Health Sciences Center, Toronto, Ontario, Canada, Psychiatric Neurogenetics Lab, Centre for Addiction and Mental Health, Toronto, Ontario, Canada, Departments of Psychiatry, Pediatrics, and Pharmacology, Vanderbilt Kennedy Center for Research on Human Development and Vanderbilt Brain Institute, Nashville, Tennessee, Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, Department of Psychiatry and Human Behavior, Brown Medical School, Butler Hospital, Providence, Rhode Island, Department of Psychiatry and Biobehavioral Sciences, School of Medicine, University of California, Los Angeles, California, Department of Psychiatry and The Behavioral Sciences, Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, California, Department of Psychiatry, College of Physicians and Surgeons at Columbia University and the New York State Psychiatric Institute, New York, New York, Partners Psychiatry and Mental Health, Belmont, Massachusetts, Department of Psychiatry, Institute for Juvenile Research, University of Illinois at Chicago, Chicago, Illinois, Department of Psychiatry, University of California, San Francisco, California, Department of Psychiatry, University of British Columbia, A3‐118, West 28th Avenue, Vancouver, BC, Canada V5Z 4H4., McLean Hospital, Belmont, Massachusetts, Department of Psychiatry, Massachusetts General Hospital, Boston, Massachusetts, Psychiatric and Neurodevelopmental Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts, Harvard Medical School, Boston, Massachusetts, University of British Columbia, Vancouver, British Columbia, Canada, British Columbia Mental Health and Addictions Research Institute Vancouver, British Columbia, Canada, Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, Ontario, Canada, Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Boston, Massachusetts, Department of Neurology, Massachusetts General Hospital, Boston, Massachusetts, Department of Neurology, Brigham and Women's Hospital, Boston, Massachusetts, Intramural Research Program, NIMH, Bethesda, Maryland, CNS Clinical Biomarker Group, Pharma Research and Early Development, F. Hoffmann‐La Roche Ltd., Basel, Switzerland

مصطلحات موضوعية: Meta‐Analysis, SLC1A1, Glutamate, Candidate Gene, OCD, Obsessive‐Compulsive Disorder, Medicine (General), Health Sciences

وصف الملف: application/pdf

Relation: Stewart, S.E.; Mayerfeld, C.; Arnold, P.D.; Crane, J.R.; O'Dushlaine, C.; Fagerness, J.A.; Yu, D.; Scharf, J.M.; Chan, E.; Kassam, F.; Moya, P.R.; Wendland, J.R.; Delorme, R.; Richter, M.A.; Kennedy, J.L.; Veenstra‐vanderweele, J.; Samuels, J.; Greenberg, B.D.; McCracken, J.T.; Knowles, J.A.; Fyer, A.J.; Rauch, S.L.; Riddle, M.A.; Grados, M.A.; Bienvenu, O.J.; Cullen, B.; Wang, Y.; Shugart, Y.Y.; Piacentini, J.; Rasmussen, S.; Nestadt, G.; Murphy, D.L.; Jenike, M.A.; Cook, E.H.; Pauls, D.L.; Hanna, G.L.; Mathews, C.A. (2013). "Metaâ analysis of association between obsessiveâ compulsive disorder and the 3â ² region of neuronal glutamate transporter gene SLC1A1 ." American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 162(4): 367-379.; https://hdl.handle.net/2027.42/98412; American Journal of Medical Genetics Part B: Neuropsychiatric Genetics; American Psychiatric Association. 2000. Diagnostic criteria from DSM‐IV‐TR. Washington, D.C: American Psychiatric Association. Vol. xii, p 370.; Arnold PD, Sicard T, Burroughs E, Richter MA, Kennedy JL. 2006. Glutamate transporter gene SLC1A1 associated with obsessive‐compulsive disorder. Arch Gen Psychiatry 63 ( 7 ): 760 – 769.; Bacanu SA. 2012. On optimal gene‐based analysis of genome scans. Genet Epidemiol 36 ( 4 ): 333 – 339.; Bailey CG, Ryan RM, Thoeng AD, Ng C, King K, Vanslambrouck JM, Auray‐Blais C, Vandenberg RJ, Bröer S, Rasko JE. 2011. Loss‐of‐function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria. J Clin Invest 121 ( 1 ): 446 – 453.; Barrett JC, Fry B, Maller J, Daly MJ. 2005. Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics 21 ( 2 ): 263 – 265.; Bogetto F, Venturello S, Albert U, Maina G, Ravizza L. 1999. Gender‐related clinical differences in obsessive‐compulsive disorder. Eur Psychiatry 14 ( 8 ): 434 – 441.; Cavallini MC, Pasquale L, Bellodi L, Smeraldi E. 1999. Complex segregation analysis for obsessive compulsive disorder and related disorders. Am J Med Genet 88 ( 1 ): 38 – 43.; Chakrabarty K, Bhattacharyya S, Christopher R, Khanna S. 2005. Glutamatergic dysfunction in OCD. Neuropsychopharmacology 30 ( 9 ): 1735 – 1740.; Cichon S, Craddock N, Daly M, Faraone SV, Gejman PV, Kelsoe J, Lehner T, Levinson DF, Moran A, Sklar P, Sullivan PF. 2009. Genomewide association studies: History, rationale, and prospects for psychiatric disorders. Am J Psychiatry 166 ( 5 ): 540 – 556.; Consortium MDDWGotPG. 2012. A mega‐analysis of genome‐wide association studies for major depressive disorder. Mol Psychiatry Epub ahead of print.; Coric V, Taskiran S, Pittenger C, Wasylink S, Mathalon DH, Valentine G, Saksa J, Wu YT, Gueorguieva R, Sanacora G, Malison RT, Krystal JH. 2005. Riluzole augmentation in treatment‐resistant obsessive‐compulsive disorder: An open‐label trial. Biol Psychiatry 58 ( 5 ): 424 – 428.; de Bakker PI, Ferreira MA, Jia X, Neale BM, Raychaudhuri S, Voight BF. 2008. Practical aspects of imputation‐driven meta‐analysis of genome‐wide association studies. Hum Mol Genet 17 ( R2 ): R122 – R128.; Yucel M, Wood SJ, Wellard RM, Harrison BJ, Fornito A, Pujol J, Velakoulis D, Pantelis C. 2008. Anterior cingulate glutamate–glutamine levels predict symptom severity in women with obsessive‐compulsive disorder. Aust N Z J Psychiatry 42 ( 6 ): 467 – 477.; Hanna GL, Fischer DJ, Chadha KR, Himle JA, Van Etten M. 2005b. Familial and sporadic subtypes of early‐onset obsessive‐compulsive disorder. Biol Psychiatry 57 ( 8 ): 895 – 900.; Hanna GL, Veenstra‐VanderWeele J, Cox NJ, Boehnke M, Himle JA, Curtis GC, Leventhal BL, Cook EH Jr. 2002. Genome‐wide linkage analysis of families with obsessive‐compulsive disorder ascertained through pediatric probands. Am J Med Genet 114 ( 5 ): 541 – 552.; Hanna GL, Veenstra‐Vanderweele J, Cox NJ, Van Etten M, Fischer DJ, Himle JA, Bivens NC, Wu X, Roe CA, Hennessy KA, Dickel DE, Leventhal BL, Cook EH. 2007. Evidence for a susceptibility locus on chromosome 10p15 in early‐onset obsessive‐compulsive disorder. Biol Psychiatry 62 ( 8 ): 856 – 862.; Hemmings SM, Stein DJ. 2006. The current status of association studies in obsessive‐compulsive disorder. Psychiatr Clin North Am 29 ( 2 ): 411 – 444.; Huang H, Chanda P, Alonso A, Bader JS, Arking DE. 2011. Gene‐based tests of association. PLoS Genet 7 ( 7 ): e1002177.; Infante‐Rivard C, Mirea L, Bull SB. 2009. Combining case–control and case‐trio data from the same population in genetic association analyses: Overview of approaches and illustration with a candidate gene study. Am J Epidemiol 170 ( 5 ): 657 – 664.; Inouye E. 1965. Similar and dissimilar manifestations of obsessive‐compulsive neuroses in monozygotic twins. Am J Psychiatry 121: 1171 – 1175.; Ivarsson T, Melin K, Wallin L. 2008. Categorical and dimensional aspects of co‐morbidity in obsessive‐compulsive disorder (OCD). Eur Child Adolesc Psychiatry 17 ( 1 ): 20 – 31.; Kanai Y, Hediger MA. 2004. The glutamate/neutral amino acid transporter family SL C1: Molecular, physiological and pharmacological aspects. Pflugers Arch 447 ( 5 ): 469 – 479.; Karno M, Golding JM, Sorenson SB, Burnam MA. 1988. The epidemiology of obsessive‐compulsive disorder in five US communities. Arch Gen Psychiatry 45 ( 12 ): 1094 – 1099.; Kazeem GR, Farrall M. 2005. Integrating case–control and TDT studies. Ann Hum Genet 69 ( Pt 3 ): 329 – 335.; Kessler RC, Chiu WT, Demler O, Merikangas KR, Walters EE. 2005. Prevalence, severity, and comorbidity of 12‐month DSM‐IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 62 ( 6 ): 617 – 627.; Kwon JS, Joo YH, Nam HJ, Lim M, Cho EY, Jung MH, Choi JS, Kim B, Kang DH, Oh S, Park T, Hong KS. 2009. Association of the glutamate transporter gene SLC1A1 with atypical antipsychotics‐induced obsessive‐compulsive symptoms. Arch Gen Psychiatry 66 ( 11 ): 1233 – 1241.; Laird NM, Horvath S, Xu X. 2000. Implementing a unified approach to family‐based tests of association. Genet Epidemiol 19 ( Suppl 1 ): S36 – S42.; Lambert JC, Grenier‐Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, Alvarez V, Sims R, Gerrish A, Chapman J, Deniz‐Naranjo C, Solfrizzi V, Sorbi S, Arosio B, Spalletta G, Siciliano G, Epelbaum J, Hannequin D, Dartigues JF, Tzourio C, Berr C, Schrijvers EM, Rogers R, Tosto G, Pasquier F, Bettens K, Van Cauwenberghe C, Fratiglioni L, Graff C, Delepine M, Ferri R, Reynolds CA, Lannfelt L, Ingelsson M, Prince JA, Chillotti C, Pilotto A, Seripa D, Boland A, Mancuso M, Bossù P, Annoni G, Nacmias B, Bosco P, Panza F, Sanchez‐Garcia F, Del Zompo M, Coto E, Owen M, O'Donovan M, Valdivieso F, Caffara P, Scarpini E, Combarros O, Buée L, Campion D, Soininen H, Breteler M, Riemenschneider M, Van Broeckhoven C, Alpérovitch A, Lathrop M, Trégouët DA, Williams J, Amouyel P. 2012. Genome‐wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Mol Psychiatry Epub ahead of print.; Lange C, DeMeo D, Silverman EK, Weiss ST, Laird NM. 2004. PBAT: Tools for family‐based association studies. Am J Hum Genet 74 ( 2 ): 367 – 369.; Langley AK, Lewin AB, Bergman RL, Lee JC, Piacentini J. 2010. Correlates of comorbid anxiety and externalizing disorders in childhood obsessive compulsive disorder. Eur Child Adolesc Psychiatry 19 ( 8 ): 637 – 645.; Lensi P, Cassano GB, Correddu G, Ravagli S, Kunovac JL, Akiskal HS. 1996. Obsessive‐compulsive disorder. Familial‐developmental history, symptomatology, comorbidity and course with special reference to gender‐related differences. Br J Psychiatry 169 ( 1 ): 101 – 107.; Wu K, Hanna GL, Rosenberg DR, Arnold PD. 2012. The role of glutamate signaling in the pathogenesis and treatment of obsessive‐compulsive disorder. Pharmacol Biochem Behav 100 ( 4 ): 726 – 735.; Zohar J, Gross‐Isseroff R, Hermesh H, Weizman A. 1999. Is there sexual dimorphism in obsessive‐compulsive disorder ? Neurosci Biobehav Rev 23 ( 6 ): 845 – 849.; Willour VL, Yao Shugart Y, Samuels J, Grados M, Cullen B, Bienvenu OJ, Wang Y, Liang KY, Valle D, Hoehn‐Saric R, Riddle M, Nestadt G. 2004b. Replication study supports evidence for linkage to 9p24 in obsessive‐compulsive disorder. Am J Hum Genet 75 ( 3 ): 508 – 513.; Willour VL, Yao Shugart, Samuels Y, Grados J, Cullen M, Bienvenu B, Wang OJ III, Liang Y, Valle KY, Hoehn‐Saric D, Riddle R, Nestadt MG. 2004a. Replication study supports evidence for linkage to 9p24 in obsessive‐compulsive disorder. Am J Hum Genet 75 ( 3 ): 508 – 513.; Whiteside SP, Port JD, Deacon BJ, Abramowitz JS. 2006. A magnetic resonance spectroscopy investigation of obsessive‐compulsive disorder and anxiety. Psychiatry Res 146 ( 2 ): 137 – 147.; Wendland JR, Moya PR, Timpano KR, Anavitarte AP, Kruse MR, Wheaton MG, Ren‐Patterson RF, Murphy DL. 2009. A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive‐compulsive disorder. Arch Gen Psychiatry 66 ( 4 ): 408 – 416.; Welch JM, Lu J, Rodriguiz RM, Trotta NC, Peca J, Ding JD, Feliciano C, Chen M, Adams JP, Luo J, Dudek SM, Weinberg RJ, Calakos N, Wetsel WC, Feng G. 2007. Cortico‐striatal synaptic defects and OCD‐like behaviours in Sapap3‐mutant mice. Nature 448 ( 7156 ): 894 – 900.; Weissman MM, Bland RC, Canino GJ, Greenwald S, Hwu HG, Lee CK, Newman SC, Oakley‐Browne MA, Rubio‐Stipec M, Wickramaratne PJ, et al. 1994. The cross national epidemiology of obsessive compulsive disorder. The Cross National Collaborative Group. J Clin Psychiatry (Suppl 55 ): 5 – 10.; Wang Y, Adamczyk A, Shugart YY, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Bienvenu OJ, Riddle M, Liang KY, Valle D, Wang T, Nestadt G. 2010. A screen of SLC1A1 for OCD‐related alleles. Am J Med Genet Part B 153B ( 2 ): 675 – 679.; Walitza S, Wendland JR, Gruenblatt E, Warnke A, Sontag TA, Tucha O, Lange KW. 2010. Genetics of early‐onset obsessive‐compulsive disorder. Eur Child Adolesc Psychiatry 19 ( 3 ): 227 – 235.; Veenstra‐VanderWeele J, Xu T, Ruggiero AM, Anderson LR, Jones ST, Himle JA, Kennedy JL, Richter MA, Hanna GL, Arnold PD. 2012. Functional studies and rare variant screening of SLC1A1/EAAC1 in males with obsessive‐compulsive disorder. Psychiatr Genet 22 ( 5 ): 256 – 260.; Veenstra‐VanderWeele J, Kim SJ, Gonen D, Hanna GL, Leventhal BL, Cook EH Jr. 2001. Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early‐onset obsessive‐compulsive disorder. Mol Psychiatry 6 ( 2 ): 160 – 167.; van Grootheest DS, Cath DC, Beekman AT, Boomsma DI. 2005. Twin studies on obsessive‐compulsive disorder: A review. Twin Res Hum Genet 8 ( 5 ): 450 – 458.; Tukel R, Polat A, Genc A, Bozkurt O, Atli H. 2004. Gender‐related differences among Turkish patients with obsessive‐compulsive disorder. Compr Psychiatry 45 ( 5 ): 362 – 366.; Dickel DE, Veenstra‐VanderWeele J, Cox NJ, Wu X, Fischer DJ, Van Etten‐Lee M, Himle JA, Leventhal BL, Cook EH Jr, Hanna GL. 2006. Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early‐onset obsessive‐compulsive disorder. Arch Gen Psychiatry 63 ( 7 ): 778 – 785.; Fischer DJ, Himle JA, Hanna GL. 1996. Age and gender effects on obsessive‐compulsive symptoms in children and adults. Depress Anxiety 4 ( 5 ): 237 – 239.; Geller DA, Biederman J, Griffin S, Jones J, Lefkowitz TR. 1996. Comorbidity of juvenile obsessive‐compulsive disorder with disruptive behavior disorders. J Am Acad Child Adolesc Psychiatry 35 ( 12 ): 1637 – 1646.; Grados M, Wilcox HC. 2007. Genetics of obsessive‐compulsive disorder: A research update. Expert Rev Neurother 7 ( 8 ): 967 – 980.; Grant P, Lougee L, Hirschtritt M, Swedo SE. 2007. An open‐label trial of riluzole, a glutamate antagonist, in children with treatment‐resistant obsessive‐compulsive disorder. J Child Adolesc Psychopharmacol 17 ( 6 ): 761 – 767.; Hanna GL, Fingerlin TE, Himle JA, Boehnke M. 2005a. Complex segregation analysis of obsessive‐compulsive disorder in families with pediatric probands. Hum Hered 60 ( 1 ): 1 – 9.; Trikalinos TA, Salanti G, Zintzaras E, Ioannidis JP. 2008. Meta‐analysis methods. Adv Genet 60: 311 – 334.; Aboujaoude E, Barry JJ, Gamel N. 2009. Memantine augmentation in treatment‐resistant obsessive‐compulsive disorder: An open‐label trial. J Clin Psychopharmacol 29 ( 1 ): 51 – 55.; Taylor S. 2012. Molecular genetics of obsessive‐compulsive disorder: A comprehensive meta‐analysis of genetic association studies. Mol Psychiatry Epub ahead of print.; Swedo SE, Schapiro MB, Grady CL, Cheslow DL, Leonard HL, Kumar A, Friedland R, Rapoport SI, Rapoport JL. 1989. Cerebral glucose metabolism in childhood‐onset obsessive‐compulsive disorder. Arch Gen Psychiatry 46 ( 6 ): 518 – 523.; Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, Illman C, Mayerfeld C, Konkashbaev A, Liu C, Pluzhnikov A, Tikhomirov A, Edlund CK, Rauch SL, Moessner R, Falkai P, Maier W, Ruhrmann S, Grabe HJ, Lennertz L, Wagner M, Bellodi L, Cavallini MC, Richter MA, Cook EH, Kennedy JL, Rosenberg D, Stein DJ, Hemmings SM, Lochner C, Azzam A, Chavira DA, Fournier E, Garrido H, Sheppard B, Umaña P, Murphy DL, Wendland JR, Veenstra‐Vanderweele J, Denys D, Blom R, Deforce D, Van Nieuwerburgh F, Westenberg HG, Walitza S, Egberts K, Renner T, Miguel EC, Cappi C, Hounie AG, Conceição do, Rosário M, Sampaio AS, Vallada H, Nicolini H, Lanzagorta N, Camarena B, Delorme R, Leboyer M, Pato CN, Pato MT, Voyiaziakis E, Heutink P, Cath DC, Posthuma D, Smit JH, Samuels J, Bienvenu OJ, Cullen B, Fyer AJ, Grados MA, Greenberg BD, McCracken JT, Riddle MA, Wang Y, Coric V, Leckman JF, Bloch M, Pittenger C, Eapen V, Black DW, Ophoff RA, Strengman E, Cusi D, Turiel M, Frau F, Macciardi F, Gibbs JR, Cookson MR, Singleton A, Hardy J, Crenshaw AT, Parkin MA, Mirel DB, Conti DV, Purcell S, Nestadt G, Hanna GL, Jenike MA, Knowles JA, Cox N, Pauls DL, Consortium ftNABE, Database ftUBE. 2012. Genome‐wide association study of obsessive‐compulsive disorder. Mol Psychiatry Epub ahead of print.; Stewart SE, Rosario MC, Brown TA, Carter AS, Leckman JF, Sukhodolsky D, Katsovitch L, King R, Geller D, Pauls DL. 2007b. Principal components analysis of obsessive‐compulsive disorder symptoms in children and adolescents. Biol Psychiatry 61 ( 3 ): 285 – 291.; Stewart SE, Rosario MC, Baer L, Carter AS, Brown TA, Scharf JM, Illmann C, Leckman JF, Sukhodolsky D, Katsovich L, Rasmussen S, Goodman W, Delorme R, Leboyer M, Chabane N, Jenike MA, Geller DA, Pauls DL. 2008. Four‐factor structure of obsessive‐compulsive disorder symptoms in children, adolescents, and adults. J Am Acad Child Adolesc Psychiatry 47 ( 7 ): 763 – 772.; Stewart SE, Jenike EA, Hezel DM, Stack DE, Dodman NH, Shuster L, Jenike MA. 2010. A single‐blinded case–control study of memantine in severe obsessive‐compulsive disorder. J Clin Psychopharmacol 30 ( 1 ): 34 – 39.; Stewart SE, Fagerness JA, Platko J, Smoller JW, Scharf JM, Illmann C, Jenike E, Chabane N, Leboyer M, Delorme R, Jenike MA, Pauls DL. 2007a. Association of the SLC1A1 glutamate transporter gene and obsessive‐compulsive disorder. Am J Med Genet Part B 144B ( 8 ): 1027 – 1033.; Smith CP, Weremowicz S, Kanai Y, Stelzner M, Morton CC, Hediger MA. 1994. Assignment of the gene coding for the human high‐affinity glutamate transporter EAAC1 to 9p24: Potential role in dicarboxylic aminoaciduria and neurodegenerative disorders. Genomics 20 ( 2 ): 335 – 336.; Shugart YY, Wang Y, Samuels JF, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Rasmussen SA, Cullen B, Hoehn‐Saric R, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Bienvenu OJ, Riddle MA, Liang KY, Nestadt G. 2009. A family‐based association study of the glutamate transporter gene SLC1A1 in obsessive‐compulsive disorder in 378 families. Am J Med Genet Part B 150B ( 6 ): 886 – 892.; Shugart YY, Samuels J, Willour VL, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Wang Y, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Page J, Rasmussen SA, Bienvenu OJ, Hoehn‐Saric R, Valle D, Liang KY, Riddle MA, Nestadt G. 2006b. Genomewide linkage scan for obsessive‐compulsive disorder: Evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol Psychiatry 11 ( 8 ): 763 – 770.; Shugart YY, Samuels J, Willour VL, Grados MA, Greenberg BD, Knowles JA, McCracken JT, Rauch SL, Murphy DL, Wang Y, Pinto A, Fyer AJ, Piacentini J, Pauls DL, Cullen B, Page J, Rasmussen SA, Bienvenu OJ, Hoehn‐Saric R, Valle D, Liang KY, Riddle MA, Nestadt G. 2006a. Genomewide linkage scan for obsessive‐compulsive disorder: Evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol Psychiatry 11 ( 8 ): 763 – 770.; Saxena S, Rauch SL. 2000. Functional neuroimaging and the neuroanatomy of obsessive‐compulsive disorder. Psychiatr Clin North Am 23 ( 3 ): 563 – 586.; Samuels J, Wang Y, Riddle MA, Greenberg BD, Fyer AJ, McCracken JT, Rauch SL, Murphy DL, Grados MA, Knowles JA, Piacentini J, Cullen B, Bienvenu OJ III, Rasmussen SA, Geller D, Pauls DL, Liang KY, Shugart YY, Nestadt G. 2011. Comprehensive family‐based association study of the glutamate transporter gene SLC1A1 in obsessive‐compulsive disorder. Am J Med Genet Part B 156B ( 4 ): 472 – 477.; Sampaio AS, Fagerness J, Crane J, Leboyer M, Delorme R, Pauls DL, Stewart SE. 2011. Association between polymorphisms in GRIK2 gene and obsessive‐compulsive disorder: A family‐based study. CNS Neurosci Ther 17 ( 3 ): 141 – 147.; Ross J, Badner J, Garrido H, Sheppard B, Chavira DA, Grados M, Woo JM, Doo P, Umaña P, Fournier E, Murray SS, Mathews CA. 2011. Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD. Hum Genet 130 ( 6 ): 795 – 805.; Rosenberg DR, Mirza Y, Russell A, Tang J, Smith JM, Banerjee SP, Bhandari R, Rose M, Ivey J, Boyd C, Moore GJ. 2004. Reduced anterior cingulate glutamatergic concentrations in childhood OCD and major depression versus healthy controls. J Am Acad Child Adolesc Psychiatry 43 ( 9 ): 1146 – 1153.; Risch NJ. 2000. Searching for genetic determinants in the new millennium. Nature 405 ( 6788 ): 847 – 856.; Ravizza L, Maina G, Bogetto F. 1997. Episodic and chronic obsessive‐compulsive disorder. Depress Anxiety 6 ( 4 ): 154 – 158.; Rauch SL, Jenike MA, Alpert NM, Baer L, Breiter HC, Savage CR, Fischman AJ. 1994. Regional cerebral blood flow measured during symptom provocation in obsessive‐compulsive disorder using oxygen 15‐labeled carbon dioxide and positron emission tomography. Arch Gen Psychiatry 51 ( 1 ): 62 – 70.; Purcell S, Neale B, Todd‐Brown K, Thomas L, Ferreira MA, Bender D, Maller J, Sklar P, de Bakker PI, Daly MJ, Sham PC. 2007. PLINK: A tool set for whole‐genome association and population‐based linkage analyses. Am J Hum Genet 81 ( 3 ): 559 – 575.; Purcell S, Cherny SS, Sham PC. 2003. Genetic power calculator: Design of linkage and association genetic mapping studies of complex traits. Bioinformatics 19 ( 1 ): 149 – 150.; Pittenger C, Krystal JH, Coric V. 2006. Glutamate‐modulating drugs as novel pharmacotherapeutic agents in the treatment of obsessive‐compulsive disorder. NeuroRx 3 ( 1 ): 69 – 81.; Pittenger C, Bloch MH, Williams K. 2011. Glutamate abnormalities in obsessive compulsive disorder: Neurobiology, pathophysiology, and treatment. Pharmacol Ther 132 ( 3 ): 314 – 332.; Pato MT, Pato CN, Pauls DL. 2002. Recent findings in the genetics of OCD. J Clin Psychiatry 63 ( Suppl 6 ): 30 – 33.; Nicolini H, Arnold P, Nestadt G, Lanzagorta N, Kennedy JL. 2009. Overview of genetics and obsessive‐compulsive disorder. Psychiatry Res 170 ( 1 ): 7 – 14.; Nicodemus KK. 2008. Catmap: Case–control and TDT meta‐analysis package. BMC Bioinformatics 9: 130.; Nestadt G, Samuels J, Riddle M, Bienvenu OJ III, Liang KY, LaBuda M, Walkup J, Grados M, Hoehn‐Saric R. 2000b. A family study of obsessive‐compulsive disorder. Arch Gen Psychiatry 57 ( 4 ): 358 – 363.; Nestadt G, Lan T, Samuels J, Riddle M, Bienvenu OJ III, Liang KY, Hoehn‐Saric R, Cullen B, Grados M, Beaty TH, Shugart YY. 2000a. Complex segregation analysis provides compelling evidence for a major gene underlying obsessive‐compulsive disorder and for heterogeneity by sex. Am J Hum Genet 67 ( 6 ): 1611 – 1616.; Nestadt G, Grados M, Samuels JF. 2010. Genetics of obsessive‐compulsive disorder. Psychiatr Clin North Am 33 ( 1 ): 141 – 158.; Menzies L, Chamberlain SR, Laird AR, Thelen SM, Sahakian BJ, Bullmore ET. 2008. Integrating evidence from neuroimaging and neuropsychological studies of obsessive‐compulsive disorder: The orbitofronto‐striatal model revisited. Neurosci Biobehav Rev 32 ( 3 ): 525 – 549.; Matsunaga H, Kiriike N, Matsui T, Miyata A, Iwasaki Y, Fujimoto K, Kasai S, Kojima M. 2000. Gender differences in social and interpersonal features and personality disorders among Japanese patients with obsessive‐compulsive disorder. Compr Psychiatry 41 ( 4 ): 266 – 272.; Mathews CA, Badner JA, Andresen JM, Sheppard B, Himle JA, Grant JE, Williams KA, Chavira DA, Azzam A, Schwartz M, Reus VI, Kim SW, Cook EH, Hanna GL. 2012. Genome‐wide linkage analysis of obsessive‐compulsive disorder implicates chromosome 1p36. Biol Psychiatry 72 ( 8 ): 629 – 636.; Mataix‐Cols D, Rosario‐Campos MC, Leckman JF. 2005. A multidimensional model of obsessive‐compulsive disorder. Am J Psychiatry 162 ( 2 ): 228 – 238.; Mah AK. 2010. SLITRK5, a protein that links striatal deficits to OCD‐like behaviours in mice. Clin Genet 78 ( 4 ): 350 – 352.; Lin DY, Zeng D. 2010. Meta‐analysis of genome‐wide association studies: No efficiency gain in using individual participant data. Genet Epidemiol 34 ( 1 ): 60 – 66.; Liang KY, Wang Y, Shugart YY, Grados M, Fyer AJ, Rauch S, Murphy D, McCracken J, Rasmussen S, Cullen B, Hoehn‐Saric R, Greenberg B, Pinto A, Knowles J, Piacentini J, Pauls D, Bienvenu O, Riddle M, Samuels J, Nestadt G. 2008. Evidence for potential relationship between SLC1A1 and a putative genetic linkage region on chromosome 14q to obsessive‐compulsive disorder with compulsive hoarding. Am J Med Genet Part B 147B ( 6 ): 1000 – 1002.

الاتاحة: https://hdl.handle.net/2027.42/98412
https://doi.org/10.1002/ajmg.b.32137

المؤلفون: Nestadt, G., Wang, Y., Grados, M.A., Riddle, M.A., Greenberg, B.D., Knowles, J.A., Fyer, A.J., McCracken, J.T., Rauch, S.L., Murphy, D.L., Rasmussen, S.A., Cullen, B., Piacentini, J., Geller, D., Pauls, D., Bienvenu, O.J., Chen, Y., Liang, K.Y., Goes, F.S., Maher, B., Pulver, A.E., Shugart, Y.Y., Valle, D., Samuels, J.F., Chang, Y.C.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 159B, issue 1, page 53-60 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.32001
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.32001
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.32001
https://onlinelibrary.wiley.com/doi/full-xml/10.1002/ajmg.b.32001

المؤلفون: Wang, Y., Adamczyk, A., Shugart, Y.Y., Samuels, J.F., Grados, M.A., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Rasmussen, S.A., Cullen, B., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Bienvenu, O.J., Riddle, M., Liang, K.Y., Valle, D., Wang, T., Nestadt, G.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 153B, issue 2, page 675-679 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.31001
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.31001
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.31001

المؤلفون: Abdulla, M.A., Edo, J., Jinam, T.A., Phipps, M.E., Ahmed, I., Brahmachari, S.K., Chaurasia, A., Jha, P., Mukerji, M., Scaria, V., Sinha, A., Assawamakin, A., Fuchareon, S., Kulawonganunchai, S., Ngamphiw, C., Tongsima, S., Bhak, J., Ghang, H., Kim, W.-Y., Lee, S., Oh, S., Yang, J.O., Yoo, H.-S., Calacal, G.C., De, Ungria M.C.A., Delfin, F.C., Perdigon, H.B., Salvador, J.M., Tabbada, K.A., Villamor, L.P., Chen, C.-H., Chen, Y.-T., Ho, S.-F., Wu, J.-Y., Chen, J., Kumar, V., Liu, E.T., Ong, R., Png, E., Seielstad, M., Tan, A., Chu, J., Cutiongco-de, La Paz E.M.C., Padilla, C.D., Gojobori, T., Koike, T., Suzuki, Y., Han, J., Xiao, H., Hoh, B.P., Sidek, M.R., Zilfalil, B.A., Huang, W., Wang, Y., Wang, H., Yuan, W., Zhao, G., Inoko, H., Oka, A., Jin, L., Jung, J., Kim, H.-L., Kim, K., Lee, J.-Y., Oh, B., Kangwanpong, D., Kampuansai, J., Srikummool, M., Kennedy, G.C., Wang, E., Khurana, P., Mandapati, K.K., Kim, S., Kimm, K., Kimura, R., Nishida, N., Ohashi, J., Tokunaga, K., Lai, P.S., Majumder, P.P., Marzuki, S., Sandraling, Y., Sudoyo, H., Suryadi, H., Mitchell, W., Naritomi, K., Palittapongarnpim, P., Sakaki, Y., Sugano, S., Xu, S., Shugart, Y.Y., Niikawa, N.

المساهمون: PAEDIATRICS

المصدر: Scopus

Relation: Abdulla, M.A., Edo, J., Jinam, T.A., Phipps, M.E., Ahmed, I., Brahmachari, S.K., Chaurasia, A., Jha, P., Mukerji, M., Scaria, V., Sinha, A., Assawamakin, A., Fuchareon, S., Kulawonganunchai, S., Ngamphiw, C., Tongsima, S., Bhak, J., Ghang, H., Kim, W.-Y., Lee, S., Oh, S., Yang, J.O., Yoo, H.-S., Calacal, G.C., De, Ungria M.C.A., Delfin, F.C., Perdigon, H.B., Salvador, J.M., Tabbada, K.A., Villamor, L.P., Chen, C.-H., Chen, Y.-T., Ho, S.-F., Wu, J.-Y., Chen, J., Kumar, V., Liu, E.T., Ong, R., Png, E., Seielstad, M., Tan, A., Chu, J., Cutiongco-de, La Paz E.M.C., Padilla, C.D., Gojobori, T., Koike, T., Suzuki, Y., Han, J., Xiao, H., Hoh, B.P., Sidek, M.R., Zilfalil, B.A., Huang, W., Wang, Y., Wang, H., Yuan, W., Zhao, G., Inoko, H., Oka, A., Jin, L., Jung, J., Kim, H.-L., Kim, K., Lee, J.-Y., Oh, B., Kangwanpong, D., Kampuansai, J., Srikummool, M., Kennedy, G.C., Wang, E., Khurana, P., Mandapati, K.K., Kim, S., Kimm, K., Kimura, R., Nishida, N., Ohashi, J., Tokunaga, K., Lai, P.S., Majumder, P.P., Marzuki, S., Sandraling, Y., Sudoyo, H., Suryadi, H., Mitchell, W., Naritomi, K., Palittapongarnpim, P., Sakaki, Y., Sugano, S., Jin, L., Xu, S., Shugart, Y.Y., Niikawa, N. (2009). Mapping human genetic diversity in Asia. Science 326 (5959) : 1541-1545. ScholarBank@NUS Repository. https://doi.org/10.1126/science.1177074; http://scholarbank.nus.edu.sg/handle/10635/25650; 000272623600059

الاتاحة: http://scholarbank.nus.edu.sg/handle/10635/25650

المؤلفون: Shugart, Y.Y., Wang, Y., Samuels, J.F., Grados, M.A., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Rasmussen, S.A., Cullen, B., Hoehn‐Saric, R., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Bienvenu, O.J., Riddle, M.A., Liang, K.Y., Nestadt, G.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 150B, issue 6, page 886-892 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.30914
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.30914
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.30914

المؤلفون: Wang, Y., Samuels, J.F., Chang, Y.C., Grados, M.A., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Rasmussen, S.A., Cullen, B., Hoehn‐Saric, R., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Bienvenu, O.J., Riddle, M., Shugart, Y.Y., Liang, K.Y., Nestadt, G.

المصدر: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics ; volume 150B, issue 1, page 33-40 ; ISSN 1552-4841 1552-485X

الاتاحة: http://dx.doi.org/10.1002/ajmg.b.30760
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.b.30760
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.b.30760

المؤلفون: Ziegler, A., Destefano, A.L., König, R., Bardel, C., Brinza, D., Bull, S., Zhaohui, C., Glaser, B., Jiang, W., Lee, K.E., Li, C.X., Li, J., Li, Xiaojian, Majoram, P., Meng, Y., Nicodemus, K.K., Platt, A., Schwarz, D.F., Shi, W., Shugart, Y.Y., Stassen, H.H., Sun, Y.V., Won, S., Wang, W., Wahba, G., Zagaar, U.A., Zhao, Z.

المساهمون: Biostatistiques santé LBBE, Département biostatistiques et modélisation pour la santé et l'environnement LBBE, Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)-Laboratoire de Biométrie et Biologie Evolutive - UMR 5558 (LBBE), Université de Lyon-Université de Lyon-VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ISSN: 0741-0395.

مصطلحات موضوعية: [SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]

Relation: hal-00698356; https://hal.science/hal-00698356

الاتاحة: https://hal.science/hal-00698356

المؤلفون: Chen, L., Velasco Mondragon, H.E., Lazcano-Ponce, E., Collins, A., Shugart, Y.Y.

Relation: Chen, L., Velasco Mondragon, H.E., Lazcano-Ponce, E., Collins, A. and Shugart, Y.Y. (2006) Effect of the peroxisome proliferators-activated receptor (PPAR) gamma 3 gene on BMI in 1,210 school students from Morelos, Mexico. Pacific Symposium on Biocomputing, 467-477.

الاتاحة: https://eprints.soton.ac.uk/59567/
http://helix-web.stanford.edu/psb06/chen_l.pdf

المؤلفون: Yang, Y.F., Qin, W., Shugart, Y.Y., He, G., Liu, X.M., Zhou, J., Zhao, X.Z., Chen, Q., La, Y.J., Xu, Y.F., Li, X.W., Gu, N.F., Feng, G.Y., Song, H., Wang, P., He, L.

المصدر: Schizophrenia Research ; volume 75, issue 1, page 11-19 ; ISSN 0920-9964

الاتاحة: http://dx.doi.org/10.1016/j.schres.2004.11.013
https://api.elsevier.com/content/article/PII:S0920996404004438?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0920996404004438?httpAccept=text/plain

المؤلفون: Davis, L.K. (Lea), Yu, D. (D.), Keenan, C.L. (Clare), Gamazon, E. (Eric), Konkashbaev, A.I. (Anuar), Derks, E.M. (Eske), Neale, B.M. (Benjamin), Yang, J. (Joanna), Lee, S.H. (Sang Hong), Evans, P., Barr, C.L. (Cathy), Bellodi, L. (Laura), Benarroch, F. (Fortu), Berrio, G.B. (Gabriel Bedoya), Bienvenu, O.J. (Oscar), Bloch, J. (Jocelyne), Blom, R.M. (Rianne), Bruun, R.D. (Ruth), Budman, C.L. (Cathy), Camarena, B. (Beatriz), Campbell, D. (Desmond), Cappi, C. (Carolina), Cardona Silgado, J.C. (Julio), Cath, D. (Daniëlle), Cavallini, M.C. (Maria), Chavira, D.A. (Denise), Chouinard, S., Conti, G. (Giario), Cook, E.H. (Edwin), Coric, V. (Vladimir), Cullen, C., Deforce, D. (Dieter), Delorme, R. (Richard), Dion, Y. (Yves), Edlund, C.K. (Christopher), Egberts, K. (Karin), Falkai, P. (Peter), Fernandez, T.V. (Thomas), Gallagher, P. (Patience), Garrido, H. (Helena), Geller, D. (Daniel), Girard, S.L. (Simon), Grabe, H.J. (Hans Jörgen), Grados, M. (Marco), Greenberg, B.D. (Benjamin), Gross-Tsur, V. (Varda), Haddad, S. (Stephen), Heiman, M.L. (Mark), Hemmings, S.M.J. (Sian), Hounie, A.G. (Ana), Illmann, C. (Cornelia), Jankovic, J. (Joseph), Jenike, M.A. (Michael), Kennedy, J.L., King, R.A., Kremeyer, B. (Barbara), Kurlan, R. (Roger), Lanzagorta, N. (Nuria), Leboyer, M. (Marion), Leckman, J.F., Lennertz, L. (Leonhard), Liu, C. (Chunyu), Lochner, C. (Christine), Lowe, T.L. (Thomas), MacCiardi, F. (Fabio), McCracken, J.T. (James), McGrath, L.M., Mesa Restrepo, S.C. (Sandra), Moessner, R. (Rainald), Morgan, J. (John), Muller, H., Murphy, D.L. (Dennis), Naarden, A.L. (Allan), Ochoa, W.C. (William Cornejo), Ophoff, R.A. (Roel), Osiecki, L. (Lisa), Pakstis, A.J., Pato, C. (Carlos), Piacentini, J. (John), Pittenger, C. (Christopher), Pollak, M.N. (Michael), Rauch, S.L. (Scott), Renner, T.J. (Tobias), Reus, V.I. (Victor), Richter, M.A. (Margaret), Riddle, M.A. (Mark), Robertson, M.M., Romero, R. (Roxana), Rosário, M.C. (Maria), Rosenberg, D. (David), Rouleau, G. (Guy), Ruhrmann, S. (Stephan), Ruiz-Linares, A. (Andres), Sampaio, A.S. (Aline), Samuels, J. (Jonathan), Sandor, P., Sheppard, B. (Brooke), Singer, H.S., Smit, J.H. (Jan), Stein, D.J. (Dan), Strengman, E. (Eric), Tischfield, J.A. (Jay), Valencia Duarte, A.V. (Ana), Vallada, H. (Homero), Nieuwerburgh, F. (Filip) van, Veenstra-Vanderweele, J. (Jeremy), Walitza, S. (Susanne), Wang, Y. (Ying), Wendland, A. (Annika), Westenberg, H.G.M. (Herman G.), Shugart, Y.Y., Miguel, E.C. (Euripedes), McMahon, W.M. (William), Wagner, M. (Michael), Nicolini, H. (Humberto), Posthuma, D. (Danielle), Hanna, G.L. (Gregory), Heutink, P. (Peter), Denys, D.A.J.P. (Damiaan), Arnold, P.D. (Paul), Oostra, B.A. (Ben), Nestadt, G. (Gerald), Freimer, N.B. (Nelson), Pauls, D.L. (David), Wray, N.R. (Naomi), Stewart, S.E., Mathews, C.A., Knowles, J.A. (James), Cox, N.J. (Nancy), Scharf, J.M.

مصطلحات الفهرس: info:eu-repo/semantics/article

URL: http://repub.eur.nl/pub/68553

المؤلفون: Maxwell, C.A. (Christopher), Benitez, J. (Javier), Gómez-Baldó, L. (Laia), Osorio, A. (Ana), Bonifaci, N. (Núria), Fernández-Ramires, R. (Ricardo), Costes, S.V. (Sylvain), Guinó, E. (Elisabet), Chen, H. (Helen), Evans, G.J.R. (Gareth), Mohan, P. (Pooja), Català, I. (Isabel), Petit, A. (Anna), Aguilar, H. (Helena), Villanueva, A. (Alberto), Aytes, A. (Alvaro), Serra-Musach, J. (Jordi), Rennert, G. (Gad), Lejbkowicz, F. (Flavio), Peterlongo, P. (Paolo), Manoukian, S. (Siranoush), Peissel, B. (Bernard), Ripamonti, C.B. (Carla), Bonnani, B. (Bernardo), Viel, A. (Alessandra), Allavena, A. (Anna), Bernard, L. (Loris), Radice, P. (Paolo), Friedman, E. (Eitan), Kaufman, B. (Bella), Laitman, Y. (Yael), Dubrovsky, M. (Maya), Milgrom, R. (Roni), Jakubowska, A. (Anna), Cybulski, C. (Cezary), Górski, B. (Bohdan), Jaworska, K. (Katarzyna), Durda, K. (Katarzyna), Sukiennicki, G. (Grzegorz), Lubinski, J. (Jan), Shugart, Y.Y., Domchek, S.M. (Susan), Letrero, R. (Richard), Hogervorst, F.B.L. (Frans), Rookus, M.A. (Matti), Collée, J.M. (Margriet), Devilee, P. (Peter), Ligtenberg, M.J. (Marjolijn), Luijt, R.B. (Rob) van der, Aalfs, C.M. (Cora), Waisfisz, Q. (Quinten), Wijnen, J.T. (Juul), Roozendaal, C.E.P. (Cornelis) van, Easton, D.F. (Douglas), Peock, S. (Susan), Cook, M. (Margaret), Oliver, C.T. (Clare), Frost, D. (Debra), harrington, P. (Patricia), Lalloo, F. (Fiona), Eeles, R. (Rosalind), Izatt, L. (Louise), Chu, C. (Chengbin), Eccles, D. (Diana), Douglas, F. (Fiona), Brewer, C. (Carole), Nevanlinna, H. (Heli), Heikinen, T. (Tuomas), Couch, F.J. (Fergus), Lindor, N.M. (Noralane), Wang, X. (Xing), Godwin, A.K. (Andrew), Caligo, M.A. (Maria), Lombardi, G. (Grazia), Loman, N. (Niklas), Karlsson, P. (Per), Ehrencrona, H. (Hans), Wachenfeldt, A. (Anna) von, Barkardottir, R.B. (Rosa), Hamann, U. (Ute), Rashid, M.U. (Muhammad), Lasa, A. (Adriana), Caldes, T. (Trinidad), Andres, R. (Raquel), Schmitt, M. (Michael), Assmann, V. (Volker), Stevens, K. (Kristen), Offit, K. (Kenneth), Curado, J. (João), Tilgner, H. (Hagen), Guigó, R. (Roderic), Aiza, G. (Gemma), Brunet, J. (Joan), Castellsagué, J. (Joan), Martrat, G. (Griselda), Urruticoechea, A. (Ander), Blanco, I. (Ignacio), Tihomirova, L. (Laima), Goldgar, D. (David), Buys, S.S. (Saundra), John, E.M. (Esther), Miron, A. (Alexander), Southey, M.C. (Melissa), Daly, M.J. (Mark), Schmutzler, R.K. (Rita), Wapenschmidt, B. (Barbara), Meindl, A. (Alfons), Arnold, N. (Norbert), Deissler, H. (Helmut), Varon-Mateeva, R. (Raymonda), Sutter, C. (Christian), Niederacher, D. (Dieter), Imyamitov, E. (Evgeny), Sinilnikova, O. (Olga), Stoppa-Lyonne, D. (Dominique), Mazoyer, S. (Sylvie), Verny-Pierre, C. (Carole), Castera, L. (Laurent), Pauw, A. (Antoine) de, Bignon, Y.-J. (Yves-Jean), Uhrhammer, N. (Nancy), Peyrat, J.-P., Vennin, P. (Philippe), Ferrer, S.F., Collonge-Rame, M.-A., Mortemousque, I. (Isabelle), Spurdle, A.B. (Amanda), Beesley, J. (Jonathan), Healey, S. (Sue), Barcellos-Hoff, M.H., Vidal, M. (Marc), Gruber, S.B. (Stephen), Lázaro, C. (Conxi), Capellá, G. (Gabriel), McGuffog, L. (Lesley), Nathanson, K.L. (Katherine), Antoniou, A.C. (Antonis), Chenevix-Trench, G. (Georgia), Fleisch, M.C. (Markus), Moreno, V. (Víctor), Pujana, M.A., Weber, B.L. (Barbara)

مصطلحات الفهرس: info:eu-repo/semantics/article

URL: http://repub.eur.nl/pub/34438
info:eu-repo/grantAgreement/EC/FP7/223175