المؤلفون: Fu, Jack M, Satterstrom, F Kyle, Peng, Minshi, Brand, Harrison, Collins, Ryan L, Dong, Shan, Wamsley, Brie, Klei, Lambertus, Wang, Lily, Hao, Stephanie P, Stevens, Christine R, Cusick, Caroline, Babadi, Mehrtash, Banks, Eric, Collins, Brett, Dodge, Sheila, Gabriel, Stacey B, Gauthier, Laura, Lee, Samuel K, Liang, Lindsay, Ljungdahl, Alicia, Mahjani, Behrang, Sloofman, Laura, Smirnov, Andrey N, Barbosa, Mafalda, Betancur, Catalina, Brusco, Alfredo, Chung, Brian HY, Cook, Edwin H, Cuccaro, Michael L, Domenici, Enrico, Ferrero, Giovanni Battista, Gargus, J Jay, Herman, Gail E, Hertz-Picciotto, Irva, Maciel, Patricia, Manoach, Dara S, Passos-Bueno, Maria Rita, Persico, Antonio M, Renieri, Alessandra, Sutcliffe, James S, Tassone, Flora, Trabetti, Elisabetta, Campos, Gabriele, Cardaropoli, Simona, Carli, Diana, Chan, Marcus CY, Fallerini, Chiara, Giorgio, Elisa, Girardi, Ana Cristina, Hansen-Kiss, Emily, Lee, So Lun, Lintas, Carla, Ludena, Yunin, Nguyen, Rachel, Pavinato, Lisa, Pericak-Vance, Margaret, Pessah, Isaac N, Schmidt, Rebecca J, Smith, Moyra, Costa, Claudia IS, Trajkova, Slavica, Wang, Jaqueline YT, Yu, Mullin HC, Cutler, David J, De Rubeis, Silvia, Buxbaum, Joseph D, Daly, Mark J, Devlin, Bernie, Roeder, Kathryn, Sanders, Stephan J, Talkowski, Michael E

المصدر: Nature Genetics. 54(9)

مصطلحات موضوعية: Biological Sciences, Bioinformatics and Computational Biology, Genetics, Brain Disorders, Stem Cell Research, Intellectual and Developmental Disabilities (IDD), Clinical Research, Mental Health, Human Genome, Mental Illness, Neurosciences, Autism, Schizophrenia, Pediatric, 2.1 Biological and endogenous factors, Mental health, Autism Spectrum Disorder, Autistic Disorder, DNA Copy Number Variations, Genetic Predisposition to Disease, Humans, Mutation, Autism Sequencing Consortium, Broad Institute Center for Common Disease Genomics, iPSYCH-BROAD Consortium, Medical and Health Sciences, Developmental Biology, Agricultural biotechnology, Bioinformatics and computational biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/04m356rr
https://escholarship.org/content/qt04m356rr/qt04m356rr.pdf

المؤلفون: Covid 19 Host Genetics Initiative, Kanai, Masahiro, Andrews, Shea, Cordioli, Mattia, Stevens, Christine, Neale, Benjamin M., Daly, Mark J., Ganna, Andrea, Pathak, Gita A., Iwasaki, Akiko, Karjalainen, Juha, Mehtonen, Juha, Pirinen, Matti, Marttila, Minttu M., Mondal, Soumyajit, Nakanishi, Tomoko, Niemi, Mari E. K., Pigazzini, Sara, Wong, Iris, Corbetta, Andrea, Ripatti, Samuli, Jermy, Bradley, Ruotsalainen, Sanni, Kristiansson, Kati, Koskelainen, Sami, Perola, Markus, Donner, Kati, Kivinen, Katja, Palotie, Aarno, Kaunisto, Mari, Bishop, Lauren, Ding, Yi, Zhou, Wei

المساهمون: Institute for Molecular Medicine Finland, Helsinki Institute of Life Science HiLIFE, Data Science Genetic Epidemiology Lab, Centre of Excellence in Complex Disease Genetics, Helsinki Institute for Information Technology, Statistical and population genetics, Department of Mathematics and Statistics, Doctoral Programme in Population Health, Institute of Biotechnology, University of Helsinki, Department of Public Health, Samuli Olli Ripatti / Principal Investigator, Complex Disease Genetics, Faculty Common Matters (Faculty of Social Sciences), Helsinki Institute of Life Science HiLIFE, Infra, Research Programs Unit, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: Ace2, Genetics, developmental biology, physiology

وصف الملف: application/pdf

Relation: Covid 19 Host Genetics Initiative , Kanai , M , Andrews , S , Cordioli , M , Stevens , C , Neale , B M , Daly , M J , Ganna , A , Kanai , M , Andrews , S , Cordioli , M , Pathak , G A , Iwasaki , A , Karjalainen , J , Mehtonen , J , Pirinen , M , Marttila , M M , Mondal , S , Nakanishi , T , Niemi , M E K , Cordioli , M , Pigazzini , S , Nakanishi , T , Wong , I , Corbetta , A , Niemi , M E K , Corbetta , A , Ripatti , S , Jermy , B , Ruotsalainen , S , Kristiansson , K , Koskelainen , S , Perola , M , Donner , K , Kivinen , K , Palotie , A , Kaunisto , M , Bishop , L , Ding , Y , Nakanishi , T & Zhou , W 2023 , ' A second update on mapping the human genetic architecture of COVID-19 ' , Nature , vol. 621 , no. 7977 , pp. E7–E26 . https://doi.org/10.1038/s41586-023-06355-3; ORCID: /0000-0002-6946-9195/work/154003021; ORCID: /0000-0002-4872-0520/work/154003079; ORCID: /0000-0001-7891-4150/work/154005011; ORCID: /0000-0002-8147-240X/work/154008573; ORCID: /0000-0002-2527-5874/work/154009781; ORCID: /0000-0002-1664-1350/work/154010095; ORCID: /0000-0002-1135-7625/work/154010888; SCOPUS: 85178660706; ORCID: /0000-0001-9190-4336/work/155648782; http://hdl.handle.net/10138/571428; 91099f6b-bc2b-4eb3-bc25-da521c380197; 001112777800001

الاتاحة: http://hdl.handle.net/10138/571428

المؤلفون: Natarajan, Pradeep, Pampana, Akhil, Graham, Sarah E, Ruotsalainen, Sanni E, Perry, James A, de Vries, Paul S, Broome, Jai G, Pirruccello, James P, Honigberg, Michael C, Aragam, Krishna, Wolford, Brooke, Brody, Jennifer A, Antonacci-Fulton, Lucinda, Arden, Moscati, Aslibekyan, Stella, Assimes, Themistocles L, Ballantyne, Christie M, Bielak, Lawrence F, Bis, Joshua C, Cade, Brian E, Do, Ron, Doddapaneni, Harsha, Emery, Leslie S, Hung, Yi-Jen, Irvin, Marguerite R, Khan, Alyna T, Lange, Leslie, Lee, Jiwon, Lemaitre, Rozenn N, Martin, Lisa W, Metcalf, Ginger, Montasser, May E, Moon, Jee-Young, Muzny, Donna, O'Connell, Jeffrey R, Palmer, Nicholette D, Peralta, Juan M, Peyser, Patricia A, Stilp, Adrienne M, Tsai, Michael, Wang, Fei Fei, Weeks, Daniel E, Yanek, Lisa R, Wilson, James G, Abecasis, Goncalo, Arnett, Donna K, Becker, Lewis C, Blangero, John, Boerwinkle, Eric, Bowden, Donald W, Chang, Yi-Cheng, Chen, Yii-Der I, Choi, Won Jung, Correa, Adolfo, Curran, Joanne E, Daly, Mark J, Dutcher, Susan K, Ellinor, Patrick T, Fornage, Myriam, Freedman, Barry I, Gabriel, Stacey, Germer, Soren, Gibbs, Richard A, He, Jiang, Hveem, Kristian, Jarvik, Gail P, Kaplan, Robert C, Kardia, Sharon LR, Kenny, Eimear, Kim, Ryan W, Kooperberg, Charles, Laurie, Cathy C, Lee, Seonwook, Lloyd-Jones, Don M, Loos, Ruth JF, Lubitz, Steven A, Mathias, Rasika A, Martinez, Karine A Viaud, McGarvey, Stephen T, Mitchell, Braxton D, Nickerson, Deborah A, North, Kari E, Palotie, Aarno, Park, Cheol Joo, Psaty, Bruce M, Rao, DC, Redline, Susan, Reiner, Alexander P, Seo, Daekwan, Seo, Jeong-Sun, Smith, Albert V, Tracy, Russell P, Vasan, Ramachandran S, Kathiresan, Sekar, Cupples, L Adrienne, Rotter, Jerome I, Morrison, Alanna C, Rich, Stephen S, Ripatti, Samuli, Willer, Cristen

المصدر: Nature communications. 12(1)

مصطلحات موضوعية: NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, FinnGen, Subcutaneous Tissue, Chromosomes, Human, X, Humans, Genetic Predisposition to Disease, Lipids, Eye Proteins, Nerve Tissue Proteins, Gene Expression Regulation, Genotype, Polymorphism, Single Nucleotide, Middle Aged, Female, Male, Genetic Loci, Genetic Association Studies, Whole Genome Sequencing, Phenomics, Cardiometabolic Risk Factors, Chromosomes, Human, X, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7701c67m

المؤلفون: Chen, Chia-Yen, Chen, Tzu-Ting, Anne Feng, Yen-Chen, Yu, Mingrui, Lin, Shu-Chin, Longchamps, Ryan J., Wang, Shi-Heng, Hsu, Yi-Hsiang, Yang, Hwai-I., Kuo, Po-Hsiu, Daly, Mark J., Chen, Wei J., Huang, Hailiang, Ge, Tian, Lin, Yen-Feng

المصدر: Cell Genomics ; volume 4, issue 9, page 100640 ; ISSN 2666-979X

الاتاحة: https://doi.org/10.1016/j.xgen.2024.100640
https://api.elsevier.com/content/article/PII:S2666979X24002441?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S2666979X24002441?httpAccept=text/plain

المؤلفون: Trsan, Tihana, Peng, Vincent, Krishna, Chirag, Ohara, Takahiro E., Beatty, Wandy L., Sudan, Raki, Kanai, Masahiro, Krishnamoorthy, Praveen, Rodrigues, Patrick Fernandes, Fachi, Jose L., Grajales-Reyes, Gary, Jaeger, Natalia, Fitzpatrick, James A.J., Cella, Marina, Gilfillan, Susan, Nakata, Toru, Jaiswal, Alok, Stappenbeck, Thaddeus S., Daly, Mark J., Xavier, Ramnik J., Colonna, Marco

المصدر: Developmental Cell ; volume 59, issue 18, page 2460-2476.e10 ; ISSN 1534-5807

الاتاحة: https://doi.org/10.1016/j.devcel.2024.06.001
https://api.elsevier.com/content/article/PII:S1534580724003794?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1534580724003794?httpAccept=text/plain

المؤلفون: gnomAD Project Consortium, Koenig, Zan, Yohannes, Mary T., Nkambule, Lethukuthula L., Zhao, Xuefang, Goodrich, Julia K., Kim, Heesu Ally, Wilson, Michael W., Tiao, Grace, Hao, Stephanie P., Sahakian, Nareh, Chao, Katherine R., Walker, Mark A., Lyu, Yunfei, Rehm, Heidi L., Neale, Benjamin M., Talkowski, Michael E., Daly, Mark J., Brand, Harrison, Karczewski, Konrad J., Atkinson, Elizabeth G., Martin, Alicia R.

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: Biomedicine

وصف الملف: application/pdf

Relation: This work was supported by funding from the National Institutes of Health (National Institute of Mental Health [NIMH] K99/ R00MH117229 to A.R.M., National Institute of Dental and Craniofacial Research R01DE031261 to H.B. and A.R.M., NIMH R01MH115957 to M.E.T., NIMH R37MH107649 to B.M.N.) and by the Novo Nordisk Foundation (NNF21SA0072102 to B.M.N. and K.J.K.). This project was also supported by funding from BroadIgnite, the Broad Next Generation Fund, and a Merkin Fellowship Award.; gnomAD Project Consortium , Koenig , Z , Yohannes , M T , Nkambule , L L , Zhao , X , Goodrich , J K , Kim , H A , Wilson , M W , Tiao , G , Hao , S P , Sahakian , N , Chao , K R , Walker , M A , Lyu , Y , Rehm , H L , Neale , B M , Talkowski , M E , Daly , M J , Brand , H , Karczewski , K J , Atkinson , E G & Martin , A R 2024 , ' A harmonized public resource of deeply sequenced diverse human genomes ' , Genome Research , vol. 34 , no. 5 , pp. 796-809 . https://doi.org/10.1101/gr.278378.123; http://hdl.handle.net/10138/585143; 036fc387-0da8-4662-b859-9f7095e89779; 85197344661

الاتاحة: http://hdl.handle.net/10138/585143

المؤلفون: Reeve, Mary Pat, Vehviläinen, Mari, Luo, Shuang, Ritari, Jarmo, Karjalainen, Juha, Gracia Tabuenca, Javier, Mehtonen, Juha, Padmanabhuni, Shanmukha Sampath, Kolosov, Nikita, Artomov, Mykyta, Siirtola, Harri, Ollila, Hanna M, Graham, Daniel, Partanen, Jukka, Xavier, Ramnik J., Daly, Mark J., Ripatti, Samuli, Salo, Tuula, Siponen, Katri-Maria

المساهمون: Tampere University, Computing Sciences

مصطلحات موضوعية: 113 Computer and information sciences

وصف الملف: fulltext

Relation: 111; Pubmed: 38776927; https://trepo.tuni.fi/handle/10024/160617

الاتاحة: https://trepo.tuni.fi/handle/10024/160617
https://doi.org/10.1016/j.ajhg.2024.04.020

المؤلفون: He, Qiang, Wang, Wenjing, Xu, Dingkang, Xiong, Yang, Tao, Chuanyuan, You, Chao, Ma, Lu, Ma, Junpeng, Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia Yen, Choi, Karmel W., Coleman, Jonathan R.I., Dalvie, Shareefa, Duncan, Laramie E., Logue, Mark W., Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Søren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babić, Dragan, Bækvad-Hansen, Marie, Baker, Dewleen G., Beckham, Jean C., Bierut, Laura J., Bisson, Jonathan I., Boks, Marco P., Bolger, Elizabeth A., Børglum, Anders D., Bradley, Bekh, Brashear, Megan, Breen, Gerome, Bryant, Richard A., Bustamante, Angela C., Bybjerg-Grauholm, Jonas, Calabrese, Joseph R., Caldas-de-Almeida, José M., Dale, Anders M., Daly, Mark J., Daskalakis, Nikolaos P., Deckert, Jürgen, Delahanty, Douglas L., Dennis, Michelle F., Disner, Seth G., Domschke, Katharina, Dzubur-Kulenovic, Alma, Erbes, Christopher R., Evans, Alexandra, Farrer, Lindsay A., Feeny, Norah C., Flory, Janine D., Forbes, David, Franz, Carol E., Galea, Sandro, Garrett, Melanie E., Gelaye, Bizu, Gelernter, Joel, Geuze, Elbert, Gillespie, Charles, Uka, Aferdita Goci, Gordon, Scott D., Guffanti, Guia, Hammamieh, Rasha, Harnal, Supriya, Hauser, Michael A., Heath, Andrew C., Hemmings, Sian M.J., Hougaard, David Michael, Jakovljevic, Miro, Jett, Marti, Johnson, Eric Otto, Jones, Ian, Jovanovic, Tanja, Qin, Xue Jun, Junglen, Angela G., Karstoft, Karen Inge, Kaufman, Milissa L., Kessler, Ronald C., Khan, Alaptagin, Kimbrel, Nathan A., King, Anthony P., Koen, Nastassja, Kranzler, Henry R., Kremen, William S., Lawford, Bruce R., Lebois, Lauren A.M., Lewis, Catrin E., Linnstaedt, Sarah D., Lori, Adriana, Lugonja, Bozo, Luykx, Jurjen J., Lyons, Michael J., Maples-Keller, Jessica, Marmar, Charles, Martin, Alicia R., Martin, Nicholas G., Maurer, Douglas, Mavissakalian, Matig R., McFarlane, Alexander, McGlinchey, Regina E., McLaughlin, Katie A., McLean, Samuel A., McLeay, Sarah, Mehta, Divya, Milberg, William P., Miller, Mark W., Morey, Rajendra A., Morris, Charles Phillip, Mors, Ole, Mortensen, Preben B., Neale, Benjamin M., Nelson, Elliot C., Nordentoft, Merete, Norman, Sonya B., O’Donnell, Meaghan, Orcutt, Holly K., Panizzon, Matthew S., Peters, Edward S., Peterson, Alan L., Peverill, Matthew, Pietrzak, Robert H., Polusny, Melissa A., Rice, John P., Ripke, Stephan, Risbrough, Victoria B., Roberts, Andrea L., Rothbaum, Alex O., Rothbaum, Barbara O., Roy-Byrne, Peter, Ruggiero, Ken, Rung, Ariane, Rutten, Bart P.F., Saccone, Nancy L., Sanchez, Sixto E., Schijven, Dick, Seedat, Soraya, Seligowski, Antonia V., Seng, Julia S., Sheerin, Christina M., Silove, Derrick, Smith, Alicia K., Smoller, Jordan W., Solovieff, Nadia, Sponheim, Scott R., Stein, Dan J., Sumner, Jennifer A., Teicher, Martin H., Thompson, Wesley K., Trapido, Edward, Uddin, Monica, Ursano, Robert J., van den Heuvel, Leigh Luella, van Hooff, Miranda, Vermetten, Eric, Vinkers, Christiaan H., Voisey, Joanne, Wang, Yunpeng, Wang, Zhewu, Werge, Thomas, Williams, Michelle A., Williamson, Douglas E., Winternitz, Sherry, Wolf, Christiane, Wolf, Erika J., Wolff, Jonathan D., Yehuda, Rachel, Young, Keith A., Young, Ross Mc D., Zhao, Hongyu, Zoellner, Lori A., Liberzon, Israel, Ressler, Kerry J., Haas, Magali, Koenen, Karestan C.

المساهمون: Cardiologie, Onderzoeksgroep 2, Brain, MGGZ, Hersenen-Medisch 1, Neurogenetica, Diagnostiek & Vroege Psychose Medisch

مصطلحات موضوعية: Psychiatry and Mental health, Cellular and Molecular Neuroscience, Biological Psychiatry

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/451380

الاتاحة: https://dspace.library.uu.nl/handle/1874/451380

المؤلفون: Estonian Biobank Research Team, FinnGen, Elliott, Amanda, Walters, Raymond K., Pirinen, Matti, Kurki, Mitja, Junna, Nella, Goldstein, Jacqueline I., Reeve, Mary Pat, Siirtola, Harri, Lemmelä, Susanna M., Turley, Patrick, Lahtela, Elisa, Mehtonen, Juha, Reis, Kadri, Elnahas, Abdelrahman G., Reigo, Anu, Palta, Priit, Esko, Tõnu, Mägi, Reedik, Palotie, Aarno, Daly, Mark J., Widén, Elisabeth

المساهمون: Tampere University, Computing Sciences

مصطلحات موضوعية: 113 Computer and information sciences, 1184 Genetics, developmental biology, physiology, 3111 Biomedicine

وصف الملف: fulltext

Relation: 56; https://trepo.tuni.fi/handle/10024/158123

الاتاحة: https://trepo.tuni.fi/handle/10024/158123
https://doi.org/10.1038/s41588-023-01607-4

المؤلفون: FinnGen, Reeve, Mary Pat, Vehviläinen, Mari, Luo, Shuang, Ritari, Jarmo, Karjalainen, Juha, Gracia-Tabuenca, Javier, Mehtonen, Juha, Padmanabhuni, Shanmukha Sampath, Kolosov, Nikita, Artomov, Mykyta, Siirtola, Harri, Olilla, Hanna M., Graham, Daniel, Partanen, Jukka, Xavier, Ramnik J., Daly, Mark J., Ripatti, Samuli, Salo, Tuula, Siponen, Maria

المساهمون: Institute for Molecular Medicine Finland, Helsinki Institute of Life Science HiLIFE, Department of Oral and Maxillofacial Diseases, HUS Head and Neck Center, Molecular and Integrative Biosciences Research Programme, Faculty Common Matters (Faculty of Social Sciences), Department of Public Health, Centre of Excellence in Complex Disease Genetics, Samuli Olli Ripatti / Principal Investigator, Complex Disease Genetics, HUSLAB

مصطلحات موضوعية: autoimmune disease, genetics, hypothyroidism, lichen planus, oral cancer, oral lichen planus, developmental biology, physiology

وصف الملف: application/pdf

Relation: N.K. and M.A. were supported by the Aging Biology Foundation . The FinnGen project is funded by two grants from Business Finland ( HUS 4685/31/2016 and UH 4386/31/2016 ) and the following industry partners: AbbVie , AstraZeneca UK Ltd , Biogen MA Inc ., Bristol-Myers Squibb (and Celgene Corporation & Celgene International II S\u00E0rl), Genentech , Merck Sharp & Dohme Corp, Pfizer Inc ., GlaxoSmithKline Intellectual Property Development Ltd ., Sanofi US Services Inc ., Maze Therapeutics Inc ., Janssen Biotech Inc , Novartis AG, and Boehringer Ingelheim .; FinnGen , Reeve , M P , Vehviläinen , M , Luo , S , Ritari , J , Karjalainen , J , Gracia-Tabuenca , J , Mehtonen , J , Padmanabhuni , S S , Kolosov , N , Artomov , M , Siirtola , H , Olilla , H M , Graham , D , Partanen , J , Xavier , R J , Daly , M J , Ripatti , S , Salo , T & Siponen , M 2024 , ' Oral and non-oral lichen planus show genetic heterogeneity and differential risk for autoimmune disease and oral cancer ' , American Journal of Human Genetics , vol. 111 , no. 6 , pp. 1047-1060 . https://doi.org/10.1016/j.ajhg.2024.04.020; ORCID: /0000-0001-6039-0088/work/161723631; ORCID: /0000-0002-5302-6429/work/161726815; http://hdl.handle.net/10138/576791; 70529083-6ee4-417b-88a1-56f70bb69379; 85194936259

الاتاحة: http://hdl.handle.net/10138/576791

المؤلفون: Estonian Biobank Res Team, Elliott, Amanda, Walters, Raymond K., Pirinen, Matti, Kurki, Mitja, Junna, Nella, Goldstein, Jacqueline I., Reeve, Mary Pat, Siirtola, Harri, Lemmelä, Susanna M., Turley, Patrick, Lahtela, Elisa, Mehtonen, Juha, Reis, Kadri, Elnahas, Abdelrahman G., Reigo, Anu, Palta, Priit, Esko, Tonu, Magi, Reedik, Metspalu, Andres, Nelis, Mari, Milani, Lili, Hudjashov, Georgi, Siirtola, Haari, Lahtinen, Elisa, Palotie, Aarno, Daly, Mark J., Widen, Elisabeth

المساهمون: Centre of Excellence in Complex Disease Genetics, Statistical and population genetics, Department of Mathematics and Statistics, Institute for Molecular Medicine Finland, Helsinki Institute of Life Science HiLIFE, Department of Public Health, Genomic Discoveries and Clinical Translation, Complex Disease Genetics, Genomics of Neurological and Neuropsychiatric Disorders, Research Programs Unit, Aarno Palotie / Principal Investigator, Elisabeth Ingrid Maria Widen / Principal Investigator

مصطلحات موضوعية: Estrogen resistance, Variants, Alpha, Risk, General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

Relation: The FinnGen project is funded by two grants from Business Finland (HUS 4685/31/2016 and UH 4386/31/2016) and by 11 industry partners (AbbVie, AstraZeneca UK, Biogen MA, Celgene Corporation, Celgene International II Sarl, Genentech, Merck Sharp & Dohme Corp, Pfizer, GlaxoSmithKline, Sanofi, Maze Therapeutics and Janssen Biotech). A.E. is a research scholar supported by the Sarnoff Cardiovascular Research Foundation, R.K.W. is supported by R01MH101244, M.P. is supported by the Academy of Finland (336825, 338507), P.T. received support by NIH/NIA (R00-AG062787) and E.W. received support from the Academy of Finland Center of Excellence program (352796). EstBB GWAS analysis is supported by research funding from the Estonian Research Council-team grants PRG1291 and PRG1911.; Estonian Biobank Res Team , Elliott , A , Walters , R K , Pirinen , M , Kurki , M , Junna , N , Goldstein , J I , Reeve , M P , Siirtola , H , Lemmelä , S M , Turley , P , Lahtela , E , Mehtonen , J , Reis , K , Elnahas , A G , Reigo , A , Palta , P , Esko , T , Magi , R , Metspalu , A , Nelis , M , Milani , L , Hudjashov , G , Siirtola , H , Lahtinen , E , Palotie , A , Daly , M J & Widen , E 2024 , ' Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes ' , Nature Genetics , vol. 56 , pp. 377–382 . https://doi.org/10.1038/s41588-023-01607-4; ORCID: /0000-0002-2527-5874/work/159455146; ORCID: /0000-0002-5953-5523/work/159455157; ORCID: /0000-0002-1664-1350/work/159455363; ORCID: /0000-0001-9320-7008/work/159455998; http://hdl.handle.net/10138/575267; d78e9c68-2a7c-4b4f-a899-71a4d6c9d9cb; 001137093800001

الاتاحة: http://hdl.handle.net/10138/575267

المؤلفون: Urpa, Lea, Kurki, Mitja I., Rahikkala, Elisa, Hämäläinen, Eija, Salomaa, Veikko, Suvisaari, Jaana, Keski-Filppula, Riikka, Rauhala, Merja, Korpi-Heikkilä, Satu, Komulainen-Ebrahim, Jonna, Helander, H, Vieira, Päivi, Uusimaa, Johanna, Moilanen, Jukka S., Körkkö, Jarmo, Singh, Tarjinder, Kuismin, Outi, Pietiläinen, Olli, Palotie, Aarno, Daly, Mark J.

المساهمون: Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Faculty of Medicine, Neuroscience Center, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator

مصطلحات موضوعية: Biomedicine, Genetics, developmental biology, physiology

وصف الملف: application/pdf

Relation: Urpa , L , Kurki , M I , Rahikkala , E , Hämäläinen , E , Salomaa , V , Suvisaari , J , Keski-Filppula , R , Rauhala , M , Korpi-Heikkilä , S , Komulainen-Ebrahim , J , Helander , H , Vieira , P , Uusimaa , J , Moilanen , J S , Körkkö , J , Singh , T , Kuismin , O , Pietiläinen , O , Palotie , A & Daly , M J 2024 , ' Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability ' , European Journal of Human Genetics , vol. 32 , pp. 576–583 . https://doi.org/10.1038/s41431-024-01581-3; ORCID: /0000-0003-4387-1861/work/159455104; ORCID: /0000-0002-2527-5874/work/159455147; ORCID: /0000-0002-8712-3518/work/159455309; http://hdl.handle.net/10138/575270; 5744e0fb-539a-4fd1-949a-77f85c84a02b; 001184734400002

الاتاحة: http://hdl.handle.net/10138/575270

المؤلفون: Rashid, Sarem, Molotkov, Ivan, Klebanov, Nikolai, Shaughnessy, Michael, Daly, Mark J., Artomov, Mykyta, Tsao, Hensin

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: Cancers

وصف الملف: application/pdf

Relation: Rashid , S , Molotkov , I , Klebanov , N , Shaughnessy , M , Daly , M J , Artomov , M & Tsao , H 2023 , ' Mendelian Randomization Analysis reveals Inverse Genetic Risks between Skin Cancers and Vitiligo ' , JID Innovations , vol. 3 , no. 6 , 100217 . https://doi.org/10.1016/j.xjidi.2023.100217; http://hdl.handle.net/10138/570793; b4d45b60-fbee-440b-ae18-d8439e33fb96; 85180870213

الاتاحة: http://hdl.handle.net/10138/570793

المؤلفون: Atkinson, Elizabeth G., Artomov, Mykyta, Loboda, Alexander A., Rehm, Heidi L., MacArthur, Daniel G., Karczewski, Konrad J., Neale, Benjamin M., Daly, Mark J.

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: Genetics, developmental biology, physiology, Statistics and probability

وصف الملف: application/pdf

Relation: We thank the members of the gnomAD and Hail teams for their assistance with this project. This project was supported by the National Institute of Mental Health (K01 MH121659 and T32 MH017119 to E.G.A.) and the National Human Genome Research Institute (U24HG011450). E.G.A. was additionally supported by the Caroline Wiess Law Fund for Research in Molecular Medicine and the ARCO Foundation Young Teacher-Investigator Fund at Baylor College of Medicine. A.A.L. was supported by the Ministry of Science and Higher Education of the Russian Federation (agreement no. 075-15-2022-301, institutional grant to Almazov National Medical Research Center). M.A. was supported by the Aging Biology Foundation and Nationwide Foundation Pediatric Innovation Fund. The All of Us Research Program is supported by the National Institutes of Health, Office of the Director: Regional Medical Centers: 1 OT2 OD026549, 1 OT2 OD026554, 1 OT2 OD026557, 1 OT2 OD026556, 1 OT2 OD026550, 1 OT2 OD 026552, 1 OT2 OD026553, 1 OT2 OD026548, 1 OT2 OD026551, 1 OT2 OD026555; IAA #: AOD 16037; Federally Qualified Health Centers: HHSN 263201600085U; Data and Research Center: 5 U2C OD023196; Biobank: 1 U24 OD023121; The Participant Center: U24 OD023176; Participant Technology Systems Center: 1 U24 OD023163; Communications and Engagement: 3 OT2 OD023205, 3 OT2 OD023206; and Community Partners: 1 OT2 OD025277, 3 OT2 OD025315, 1 OT2 OD025337, 1 OT2 OD025276. In addition, the All of Us Research Program would not be possible without the partnership of its participants.; Atkinson , E G , Artomov , M , Loboda , A A , Rehm , H L , MacArthur , D G , Karczewski , K J , Neale , B M & Daly , M J 2023 , ' Discordant calls across genotype discovery approaches elucidate variants with systematic errors ' , Genome Research , vol. 33 , no. 6 , pp. 999-1005 . https://doi.org/10.1101/gr.277908.123; http://hdl.handle.net/10138/571294; a2d804ed-750c-4005-bba3-7782cac2458a; 85165521323

الاتاحة: http://hdl.handle.net/10138/571294

المؤلفون: Chen, Chia Yen, Chen, Tzu Ting, Feng, Yen Chen Anne, Yu, Mingrui, Lin, Shu Chin, Longchamps, Ryan J., Wang, Shi Heng, Hsu, Yi Hsiang, Yang, Hwai I., Kuo, Po Hsiu, Daly, Mark J., Chen, Wei J., Huang, Hailiang, Ge, Tian, Lin, Yen Feng

المساهمون: Institute for Molecular Medicine Finland

مصطلحات موضوعية: cross-ancestry GWAS, multi-polygenic score prediction, quantitative traits, Taiwan Biobank, Genetics, developmental biology, physiology

وصف الملف: application/pdf

Relation: We thank Masahiro Kanai for helpful discussions related to Biobank Japan (BBJ). We thank Saori Sakaue for the help with making Figure 2 A. We thank the participants of Taiwan Biobank and the staff, management team, and leadership of Taiwan Biobank. We thank Neale Lab, UK Biobank, and Biobank Japan for providing resources and releasing the genome-wide association summary statistics that made this study possible. Y.-F.L. is supported by the National Health Research Institutes ( NP-110 , 111 , 112-PP-09 ) and the Ministry of Science and Technology (MOST 109-2314-B-400-017 , 110-2314-B-400-028-MY3 ) of Taiwan. Y.-C.A.F. acknowledges support from the National Taiwan University ( NTU-112L7404 ), the Yushan Young Fellow Program by the Ministry of Education (MOE; NTU-112V1020-2 ), and the National Science and Technology Council (NSTC 112-2314-B-002-200-MY3 ). Y.-C.A.F. and P.-H.K. are supported by the Population Health Research Center from Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the MOE in Taiwan ( NTU-112L9004 ). T.G. is supported by NHGRI R01HG012354 , U01HG008685 , and U01HG011723 . H.H. acknowledges support from NIDDK K01DK114379 , NIMH U01MH109539 , Brain & Behavior Research Foundation Young Investigator Grant, the Zhengxu and Ying He Foundation , and the Stanley Center for Psychiatric Research . This research has been conducted using the Taiwan Biobank resource. We thank the National Center for Genome Medicine of Taiwan for the technical support in genotyping. We thank the National Core Facility for Biopharmaceuticals (NCFB, MOST 106-2319-B-492-002 ) and National Center for High-performance Computing (NCHC) of National Applied Research Laboratories (NARLabs) of Taiwan for providing computational and storage resources. We thank Masahiro Kanai for helpful discussions related to Biobank Japan (BBJ). We thank Saori Sakaue for the help with making Figure 2A. We thank the participants of Taiwan Biobank and the staff, management team, and leadership of Taiwan Biobank. We thank Neale Lab, UK Biobank, and Biobank Japan for providing resources and releasing the genome-wide association summary statistics that made this study possible. Y.-F.L. is supported by the National Health Research Institutes (NP-110, 111, 112-PP-09) and the Ministry of Science and Technology (MOST 109-2314-B-400-017, 110-2314-B-400-028-MY3) of Taiwan. Y.-C.A.F. acknowledges support from the National Taiwan University (NTU-112L7404), the Yushan Young Fellow Program by the Ministry of Education (MOE; NTU-112V1020-2), and the National Science and Technology Council (NSTC 112-2314-B-002-200-MY3). Y.-C.A.F. and P.-H.K. are supported by the Population Health Research Center from Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by the MOE in Taiwan (NTU-112L9004). T.G. is supported by NHGRI R01HG012354, U01HG008685, and U01HG011723. H.H. acknowledges support from NIDDK K01DK114379, NIMH U01MH109539, Brain & Behavior Research Foundation Young Investigator Grant, the Zhengxu and Ying He Foundation, and the Stanley Center for Psychiatric Research. This research has been conducted using the Taiwan Biobank resource. We thank the National Center for Genome Medicine of Taiwan for the technical support in genotyping. We thank the National Core Facility for Biopharmaceuticals (NCFB, MOST 106-2319-B-492-002) and National Center for High-performance Computing (NCHC) of National Applied Research Laboratories (NARLabs) of Taiwan for providing computational and storage resources. Conceptualized, C.-Y.C. Y.-C.A.F. H.H. T.G. and Y.-F.L.; methodology, C.-Y.C. Y.-C.A.F. M.Y. R.J.L. H.H. and T.G.; formal analysis, T.-T.C. S.-C.L. and Y.-F.L.; resources, Y.-F.L.; writing – original draft, C.-Y.C. Y.-C.A.F. H.H. T.G. and Y.-F.L.; writing – review & editing, S.-H.W. Y.-H.H. H.-I.Y. P.-H.K. M.J.D. and W.J.C.; supervision, C.-Y.C. Y.-C.A.F. H.H. T.G. and Y.-F.L.; project administration, Y.-F.L. C.-Y.C. is an employee of Biogen. R.J.L. is an employee of Ionis Pharmaceuticals. M.J.D. is a founder of Maze Therapeutics.; Chen , C Y , Chen , T T , Feng , Y C A , Yu , M , Lin , S C , Longchamps , R J , Wang , S H , Hsu , Y H , Yang , H I , Kuo , P H , Daly , M J , Chen , W J , Huang , H , Ge , T & Lin , Y F 2023 , ' Analysis across Taiwan Biobank, Biobank Japan, and UK Biobank identifies hundreds of novel loci for 36 quantitative traits ' , Cell genomics , vol. 3 , no. 12 , 100436 . https://doi.org/10.1016/j.xgen.2023.100436; http://hdl.handle.net/10138/569322; 038cea2d-f3e9-4d49-89df-c5b2513e3fa5; 85179472249; 001141835800001

الاتاحة: http://hdl.handle.net/10138/569322

المؤلفون: International League Against Epilepsy Consortium on Complex Epilepsies, Stevelink, Remi, Campbell, Ciarán, Daly, Mark J., Kurki, Mitja I., Neale, Benjamin M., Palotie, Aarno, Heyne, Henrike O., Eriksson, Johan G., Kälviäinen, Reetta, Kantanen, Anne-Mari, Saarela, Anni, Timonen, Oskari, Lehesjoki, Anna-Elina, Linnankivi, Tarja

المساهمون: Institute for Molecular Medicine Finland, Centre of Excellence in Complex Disease Genetics, Research Programs Unit, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders, Clinicum, Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Department of Medical and Clinical Genetics, Helsinki University Hospital Area, HUS Children and Adolescents

مصطلحات موضوعية: Genetics, developmental biology, physiology, Biomedicine, Neurosciences, Public health care science, environmental and occupational health, General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

Relation: This study received support from Science Foundation Ireland (SFI; 16/RC/3948), cofunded under the European Regional Development Fund, the Research Unit FOR-2715 of the German Research Foundation (MN: NO755/6-1 and NO755/13-1), from Wellcome Trust (grant 084730), European Union’s Seventh Framework Program (FP7/2007-2013) under grant agreement 279062 (EpiPGX), The Muir Maxwell Trust and the Epilepsy Society, UK and Fonds National de la Recherche Luxembourg (Research Unit FOR-2715, FNR grant INTER/DFG/21/16394868 MechEPI2) to P.M. and R. Krause. Part of this work was undertaken at University College London Hospitals, which received a proportion of funding from the NIHR Biomedical Research Centers funding scheme. Further support was received by a ‘Vrienden WKZ’ fund 1616091 (MING) to R. Stevelink and B.P.C.K., a National Health and Medical Research Council (NHMRC) of Australia Program Grant (1091593) to S.F.B. and I.E.S. and an NHMRC Investigator grant (APP1195236) to M.B. The Australian Government Research Training Program Scholarship (APP533086) provided by the Australian Commonwealth Government and the University of Melbourne supports K.L.O., a Wellcome Clinical Ph.D. Fellowship on the 4Ward North program (203914/Z/16/Z) supported D.L.-S., the UKRI MRC award MR/S02638X/1 and the NIHR Imperial Biomedical Research Center (BRC) support M.R.J., and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP), Brazil (grant 2013/07559-3) supported I.L.-C. The funding bodies had no role in the study design, data collection, analysis and interpretation, or in writing the manuscript. We thank the Epi25 principal investigators, local staff from individual cohorts and all patients with epilepsy who participated in research studies at local centers for making possible this global collaboration and resource to advance epilepsy genetics research. This work is part of the Centers for Common Disease Genomics (CCDG) program, funded by the National Human Genome Research Institute (NHGRI), The Eunice Kennedy Shriver National Institute of Child Health and Human Development and the National Heart, Lung and Blood Institute (NHLBI). CCDG-funded Epi25 research activities at the Broad Institute, including genomic data generation in the Broad Genomics Platform, were supported by NHGRI grant UM1 HG008895 (PIs: E. Lander, S. Gabriel, M. Daly, S. Kathiresan). The Genome Sequencing Program efforts were also supported by NHGRI under grant 5U01HG009088-02. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. We thank the Stanley Center for Psychiatric Research at the Broad Institute for supporting the genomic data generation efforts as well as the aggregation of control samples and cohorts to contribute to the Epi25 GWAS analyses. In particular, the Genomic Psychiatry Cohort controls were genotyped on the GSA-MD v1.0 by the Broad Genomics Platform with funding from NIH grant U01MH105641 and the Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard. The FINRISK controls were part of the FINRISK studies supported by the THL (formerly KTL: National Public Health Institute) through budgetary funds from the government, with additional funding from institutions such as the Academy of Finland, the European Union, ministries and national and international foundations and societies to support specific research purposes. The collection of the Hong Kong Osteoporosis Study (HKOS) control samples was funded by the Bone Health Fund and Research Grants Council—Early Career Scheme (project 27100416). Other control datasets included IBD NIDDK and samples from the Mass General Brigham (MGB) Biobank available from dbGaP under study accession number phs002018.v1.p1. G.L.C. is in receipt of research funding from Congenica and Janssen Pharmaceuticals and has conducted consultancy for Ono Pharmaceuticals. S.F.B. received funding from UCB Pharma and Eisai and has been a consultant for Praxis Precision Medicines and Sequiris. Q.S.L. is an employee of Janssen Research & Development, LLC and a shareholder in Johnson & Johnson, which is the parent company of the Janssen companies. B.M.N. currently serves as a member of the scientific advisory board at Deep Genomics and Neumora (previously RBNC) and as a consultant for Camp4 Therapeutics. S.P. is an employee and shareholder of AstraZeneca. U.U., S.M., H. Stefansson and K.S. are employees of deCODE genetics/Amgen.; International League Against Epilepsy Consortium on Complex Epilepsies , Stevelink , R , Campbell , C , Daly , M J , Kurki , M I , Neale , B M , Palotie , A , Heyne , H O , Eriksson , J G , Kälviäinen , R , Kantanen , A-M , Saarela , A , Timonen , O , Lehesjoki , A-E & Linnankivi , T 2023 , ' GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture ' , Nature Genetics , vol. 55 , no. 9 , pp. 1471-1482 . https://doi.org/10.1038/s41588-023-01485-w; ORCID: /0000-0002-2527-5874/work/154009783; http://hdl.handle.net/10138/571721; f9a2f528-3f1c-41c8-b763-3e74c452709d; 85169457451; 001169861400003

الاتاحة: http://hdl.handle.net/10138/571721

المؤلفون: FinnGen, Estonian Biobank Research Team, Heyne, Henrike O., Pajuste, Fanny Dhelia, Wanner, Julian, Daniel Onwuchekwa, Jennifer I., Mägi, Reedik, Palotie, Aarno, Kälviainen, Reetta, Daly, Mark J.

المساهمون: Institute for Molecular Medicine Finland, Research Programs Unit, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: Health care science

وصف الملف: application/pdf

Relation: FinnGen , Estonian Biobank Research Team , Heyne , H O , Pajuste , F D , Wanner , J , Daniel Onwuchekwa , J I , Mägi , R , Palotie , A , Kälviainen , R & Daly , M J 2024 , ' Polygenic risk scores as a marker for epilepsy risk across lifetime and after unspecified seizure events ' , Nature Communications , vol. 15 , no. 1 , 6277 . https://doi.org/10.1038/s41467-024-50295-z; ORCID: /0000-0002-2527-5874/work/165315455; http://hdl.handle.net/10138/584490; 8387f251-d28c-4a22-a3d1-1381e22ac65a; 85199597125; 001277997800001

الاتاحة: http://hdl.handle.net/10138/584490

المؤلفون: Usoltsev, Dmitrii, Kolosov, Nikita, Rotar, Oxana, Loboda, Alexander, Boyarinova, Maria, Moguchaya, Ekaterina, Kolesova, Ekaterina, Erina, Anastasia, Tolkunova, Kristina, Rezapova, Valeriia, Molotkov, Ivan, Melnik, Olesya, Freylikhman, Olga, Paskar, Nadezhda, Alieva, Asiiat, Baranova, Elena, Bazhenova, Elena, Beliaeva, Olga, Vasilyeva, Elena, Kibkalo, Sofia, Skitchenko, Rostislav, Babenko, Alina, Sergushichev, Alexey, Dushina, Alena, Lopina, Ekaterina, Basyrova, Irina, Libis, Roman, Duplyakov, Dmitrii, Cherepanova, Natalya, Donner, Kati, Laiho, Paivi, Kostareva, Anna, Konradi, Alexandra, Shlyakhto, Evgeny, Palotie, Aarno, Daly, Mark J., Artomov, Mykyta

المساهمون: Technology Centre, Institute for Molecular Medicine Finland, Research Programs Unit, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: Chemical sciences

وصف الملف: application/pdf

Relation: Genetic data generation and contributions of K.D., P.L., A.P., M.J.D. were supported by the Finnish Academy, Center of Excellence in Disease Genetics (to A.P.). D.U., N.K., O.R., A.L., M.B., E.M., E.K., A.E., K.T., V.R., O.M., O.F., An.K., Al.K., E.S. were supported by the Ministry of Science and Higher Education of the Russian Federation (Agreement # 075-15-2022-301 to E.S.). M.A. was supported by the Aging Biology Foundation. The authors thank Dr. Maxim Artyomov (WUSTL) for his support of the project and helpful discussions.; http://hdl.handle.net/10138/584306; 85199250995; 001275549300017

الاتاحة: http://hdl.handle.net/10138/584306

المؤلفون: Koenig, Zan, Yohannes, Mary T., Nkambule, Lethukuthula L., Zhao, Xuefang, Goodrich, Julia K., Kim, Heesu Ally, Wilson, Michael W., Tiao, Grace, Hao, Stephanie P., Sahakian, Nareh, Chao, Katherine R., Walker, Mark A., Lyu, Yunfei, gnomAD Project Consortium, Rehm, Heidi L., Neale, Benjamin M., Talkowski, Michael E., Daly, Mark J., Brand, Harrison, Karczewski, Konrad J., Atkinson, Elizabeth G., Martin, Alicia R.

مصطلحات موضوعية: RESOURCES

وصف الملف: text/html

Relation: http://genome.cshlp.org/cgi/content/short/34/5/796; http://dx.doi.org/10.1101/gr.278378.123

الاتاحة: http://genome.cshlp.org/cgi/content/short/34/5/796
https://doi.org/10.1101/gr.278378.123

المؤلفون: Trastulla, Lucia, Dolgalev, Georgii, Domenici, Enrico, Haroutunian, Vahram, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hofman, Andrea, Hollegaard, Mads V., Hougaard, David M., Huang, Hailiang, Adolfsson, Rolf, Hultman, Christina M., Ikeda, Masashi, Iwata, Nakao, Jablensky, Assen V., Joa, Inge, Jonsson, Erik G., Julia, Antonio, Kahler, Anna K., Kahn, René S., Kalaydjieva, Luba, Agartz, Ingrid, Karachanak-Yankova, Sena, Karjalainen, Juha, Kavanagh, David, Keller, Matthew C., Kennedy, James L., Khrunin, Andrey, Kim, Yunjung, Kirov, George, Klovins, Janis, Knight, Jo, Agerbo, Esben, Knowles, James A., Konte, Bettina, Kucinskas, Vaidutis, Kucinskiene, Zita Ausrele, Kuzelova-Ptackova, Hana, Laurent, Claudine, Leboyer, Marion, Lee, Phil H., Keong, Jimmy Lee Chee, Legge, Sophie E., Albus, Margot, Lencz, Todd, Lerer, Bernard, Levinson, Douglas F., Li, Miaoxin, Li, Qingqin S., Li, Tao, Liang, Kung-Yee, Lieberman, Jeffrey, Limborska, Svetlana, Liu, Jianjun, Alexander, Madeline, Lonnqvist, Jouko, Loughland, Carmel M., Jan Lubinski, Macek, Milan, Magnusson, Patrik K. E., Maher, Brion S., Maier, Wolfgang, Malhotra, Anil K., Mallet, Jacques, Marsal, Sara, Amin, Farooq, Mattheisen, Manuel, Mattingsdal, Morten, McCarley, Robert W., McCarroll, Steven A., McDonald, Colm, McIntosh, Andrew M., Meier, Sandra, Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Bacanu, Silviu A., Mesholam-Gately, Raquelle I., Metspalu, Andres, Michie, Patricia T., Milani, Lili, Milanova, Vihra, Mokrab, Younes, Moran, Jennifer L., Morris, Derek W., Mors, Ole, Mortensen, Preben B., Begemann, Martin, Mowry, Bryan J., Murphy, Kieran C., Murray, Robin M., Myin-Germeys, Inez, Neale, Benjamin M., Nelis, Mari, Nenadic, Igor, Nertney, Deborah A., Nestadt, Gerald, Nicodemus, Kristin K., Belliveau, Richard A., Nikitina-Zake, Liene, Nisenbaum, Laura, Nordin, Annelie, Nothen, Markus M., O’Callaghan, Eadbhard, O’Dushlaine, Colm, O’Neill, F. Anthony, Oh, Sang-Yun, Olincy, Ann, Olsen, Line, Moser, Sylvain, Bene, Judit, Van Os, Jim, Owen, Michael J., Palotie, Aarno, Pantelis, Christos, Papadimitriou, George N., Parkhomenko, Elena, Pato, Carlos, Pato, Michele T., Paunio, Tiina, Perkins, Diana O., Bergen, Sarah E., Pers, Tune H., Petryshen, Tracey L., Pietilainen, Olli, Pimm, Jonathan, Pocklington, Andrew J., Posthuma, Danielle, Powell, John, Price, Alkes, Pulver, Ann E., Purcell, Shaun M., Bevilacqua, Elizabeth, Quested, Digby, Rasmussen, Henrik B., Reichenberg, Abraham, Reimers, Mark A., Richards, Alexander L., Riley, Brien P., Roffman, Joshua L., Roussos, Panos, Dan Rujescu, Salomaa, Veikko, Bigdeli, Tim B., Sanders, Alan R., Schall, Ulrich, Schwab, Sibylle G., Scolnick, Edward M., Scott, Rodney J., Seidman, Larry J., Sham, Pak C., Shi, Jianxin, Sigurdsson, Engilbert, Silverman, Jeremy M., Black, Donald W., Sim, Kang, Slominsky, Petr, Smoller, Jordan W., So, Hon-Cheong, Soderman, Erik, Spencer, Chris C. A., Clair, David St, Stefansson, Hreinn, Stefansson, Kari, Steinberg, Stacy, Blackwood, Douglas H. R., Stogmann, Elisabeth, Straub, Richard E., Strengman, Eric, Strohmaier, Jana, Stroup, T. Scott, Subramaniam, Mythily, Suvisaari, Jaana, Svrakic, Dragan M., Szatkiewicz, Jin P., Thirumalai, Srinivas, Borglum, Anders D., Toncheva, Draga, Tosato, Sarah, Treutlein, Jens, Visscher, Peter M., Waddington, John, Walsh, Dermot, Walters, James T. R., Wang, Dai, Wang, Qiang, Webb, Bradley T., Bramon, Elvira, Weinberger, Daniel R., Weiser, Mark, Werge, Thomas, Wildenauer, Dieter B., Williams, Nigel M., Williams, Stephanie, Witt, Stephanie H., Wolen, Aaron R., Wong, Emily H. M., Wormley, Brandon K., Bruggeman, Richard, Xi, Simon, Zai, Clement C., Zheng, Xuebin, Zimprich, Fritz, Corvin, Aiden, Fanous, Ayman H., Rietschel, Marcella, Holmans, Peter A., Andreassen, Ole A., Lee, S. Hong, Buccola, Nancy G., Sullivan, Patrick F., Ophoff, Roel A., Wray, Naomi R., Sklar, Pamela, Kendler, Kenneth S., O’Donovan, Michael C., Budde, Monika, Heilbronner, Urs, Papiol, Sergi, Teumer, Alexander, Jiménez-Barrón, Laura T., Buckner, Randy L., Homuth, Georg, Völzke, Henry, Dörr, Marcus, Falkai, Peter, Schulze, Thomas G., Gagneur, Julien, Iorio, Francesco, Müller-Myhsok, Bertram, Schunkert, Heribert, Ziller, Michael J., Bulik-Sullivan, Brendan, Buxbaum, Joseph D., Byerley, William, Cahn, Wiepke, Cai, Guiqing, Campion, Dominique, Cantor, Rita M., Carr, Vaughan J., Carrera, Noa, Andlauer, Till F. M., Catts, Stanley V., Chambert, Kimberley D., Chan, Raymond C. K., Chen, Eric Y. H., Chen, Ronald Y. L., Cheng, Wei, Cheung, Eric F. C., Chong, Siow Ann, Cichon, Sven, Cloninger, C. Robert, von Scheidt, Moritz, Cohen, David, Cohen, Nadine, Collier, David A., Cormican, Paul, Craddock, Nicholas, Crowley, James J., Daly, Mark J., Darvasi, Ariel, Davidson, Michael, Davis, Kenneth L., Ruderfer, Douglas M., Degenhardt, Franziska, Del Favero, Jurgen, Demontis, Ditte, Dikeos, Dimitris, Dinan, Timothy, Djurovic, Srdjan, Donohoe, Gary, Drapeau, Elodie, Duan, Jubao, Dudbridge, Frank, Ripke, Stephan, Ehrenreich, Hannelore, Eichhammer, Peter, Eriksson, Johan, Escott-Price, Valentina, Esko, Tonu, Essioux, Laurent, Farh, Kai-How, Farrell, Martilias S., Frank, Josef, Franke, Lude, McQuillin, Andrew, Freedman, Robert, Freimer, Nelson B., Friedman, Joseph I., Fromer, Menachem, Gejman, Pablo V., Genovese, Giulio, Georgieva, Lyudmila, Giegling, Ina, Gill, Michael, Giusti-Rodriguez, Paola, Stahl, Eli A., Godard, Stephanie, Goldstein, Jacqueline I., Gopal, Srihari, Gratten, Jacob, Gurling, Hugh, de Haan, Lieuwe, Hammer, Christian, Hamshere, Marian L., Hansen, Mark, Hansen, Thomas

المصدر: Nature Communications 15(1), 5534 (2024). doi:10.1038/s41467-024-49338-2

مصطلحات موضوعية: info:eu-repo/classification/ddc/500

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/2041-1723; https://juser.fz-juelich.de/record/1028745; https://juser.fz-juelich.de/search?p=id:%22FZJ-2024-04793%22

الاتاحة: https://juser.fz-juelich.de/record/1028745
https://juser.fz-juelich.de/search?p=id:%22FZJ-2024-04793%22