المؤلفون: Musiał, Adrianna Dominika (National Research Institute of Animal Production), Ropka-Molik, Katarzyna (National Research Institute of Animal Production), Wallner, Barbara (University of Veterinary Medicine Vienna), Bieniek, Agnieszka (National Research Institute of Animal Production), Radović, Lara (University of Veterinary Medicine Vienna), Stefaniuk-Szmukier, Monika (National Research Institute of Animal Production)

المصدر: PeerJ, 12 (2024)

مصطلحات موضوعية: Animals, Horses Genetics, DNA, Mitochondrial Genetics, Poland, Y Chromosome Genetics, Haplotypes Genetics, Male, Polymorphism, Single Nucleotide, Female, Breeding

وصف الملف: application/pdf

Relation: isPartOf:https://phaidra.vetmeduni.ac.at/o:605[Open Access Publications]; https://phaidra.vetmeduni.ac.at/o:3465

الاتاحة: https://doi.org/10.7717/peerj.17549
https://phaidra.vetmeduni.ac.at/o:3465

المؤلفون: Cavinato, T., Rubinacci, S., Malaspinas, A.S., Delaneau, O.

المصدر: Nature computational science, vol. 4, no. 5, pp. 360-366

مصطلحات موضوعية: Humans, Genome-Wide Association Study/methods, Genotype, Linkage Disequilibrium, Haplotypes/genetics, Polymorphism, Single Nucleotide/genetics, Information Dissemination/methods, Computer Simulation, Models, Genetic, Algorithms, Genome, Human/genetics, Poisson Distribution

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38745108; info:eu-repo/semantics/altIdentifier/eissn/2662-8457; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_981E899095A47; https://serval.unil.ch/notice/serval:BIB_981E899095A4; https://serval.unil.ch/resource/serval:BIB_981E899095A4.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_981E899095A4
https://doi.org/10.1038/s43588-024-00630-7
https://serval.unil.ch/resource/serval:BIB_981E899095A4.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_981E899095A47

المؤلفون: Blacher, P., De Gasperin, O., Grasso, G., Sarton-Lohéac, S., Allemann, R., Chapuisat, M.

المصدر: Molecular ecology, vol. 32, no. 5, pp. 1062-1072

مصطلحات موضوعية: Animals, Female, Ants/genetics, Polymorphism, Genetic/genetics, Genotype, Haplotypes/genetics, Reproduction/genetics, Social Behavior, ants, genetic load, inversions, social polymorphism, supergenes

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/36504171; info:eu-repo/semantics/altIdentifier/eissn/1365-294X; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_9042BFC8DFC27; https://serval.unil.ch/notice/serval:BIB_9042BFC8DFC2; https://serval.unil.ch/resource/serval:BIB_9042BFC8DFC2.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_9042BFC8DFC2
https://doi.org/10.1111/mec.16821
https://onlinelibrary.wiley.com/doi/epdf/10.1111/mec.16821
https://serval.unil.ch/resource/serval:BIB_9042BFC8DFC2.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_9042BFC8DFC27

المؤلفون: Mustamin, Yusdar, Akyol, Turgut Yigit, Gordon, Max, Manggabarani, Andi Madihah, Isomura, Yoshiko, Kawamura, Yasuko, Bamba, Masaru, Williams, Cranos, Andersen, Stig Uggerhøj, Sato, Shusei

المصدر: Mustamin , Y , Akyol , T Y , Gordon , M , Manggabarani , A M , Isomura , Y , Kawamura , Y , Bamba , M , Williams , C , Andersen , S U & Sato , S 2023 , ' FER and LecRK show haplotype-dependent cold-responsiveness and mediate freezing tolerance in Lotus japonicus ' , Plant Physiology , vol. 191 , no. 2 , pp. 1138-1152 . https://doi.org/10.1093/plphys/kiac533

مصطلحات موضوعية: Acclimatization/genetics, Adaptation, Physiological/genetics, Freezing, Gene Expression Regulation, Plant, Haplotypes/genetics, Lotus/metabolism

Relation: https://pure.au.dk/portal/da/publications/fer-and-lecrk-show-haplotypedependent-coldresponsiveness-and-mediate-freezing-tolerance-in-lotus-japonicus(30641c67-7716-43d2-aba3-7c1c6ade5704).html

الاتاحة: https://pure.au.dk/portal/da/publications/fer-and-lecrk-show-haplotypedependent-coldresponsiveness-and-mediate-freezing-tolerance-in-lotus-japonicus(30641c67-7716-43d2-aba3-7c1c6ade5704).html
https://doi.org/10.1093/plphys/kiac533
http://www.scopus.com/inward/record.url?scp=85147858383&partnerID=8YFLogxK

المساهمون: Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Kim, Eung Kweon

مصطلحات موضوعية: Body Height* / genetics, Chromosome Mapping, Europe / ethnology, Gene Frequency / genetics, Genome, Human / genetics, Genome-Wide Association Study, Haplotypes / genetics, Humans, Linkage Disequilibrium / genetics, Phenotype, Polymorphism, Single Nucleotide* / genetics, Sample Size

Relation: NATURE; J02289; OAK-2022-10218; https://ir.ymlib.yonsei.ac.kr/handle/22282913/193231; T202300814; NATURE, Vol.610(7933) : 704-712, 2022-10

الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/193231
https://doi.org/10.1038/s41586-022-05275-y

المؤلفون: 23andMe Research Team

المساهمون: CDL Onderzoek Pasterkamp, Circulatory Health, Onderzoek Precision medicine, Team Medisch, Zorgeenheid Vaatchirurgie Medisch, Regenerative Medicine and Stem Cells, Infection & Immunity, Gezonde Vaten

مصطلحات موضوعية: Body Height/genetics, Chromosome Mapping, Europe/ethnology, Gene Frequency/genetics, Genome, Human/genetics, Genome-Wide Association Study, Haplotypes/genetics, Humans, Linkage Disequilibrium/genetics, Phenotype, Polymorphism, Single Nucleotide/genetics, Sample Size, Journal Article, Research Support, N.I.H., Extramural, Non-U.S. Gov't

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/447862

الاتاحة: https://dspace.library.uu.nl/handle/1874/447862

المصدر: Juvenile Dermatomyositis Cohort Biomarker Study and Repository (UK and Ireland) , The Myositis Genetics Consortium (MYOGEN) & Childhood Myositis Heterogeneity Study Group 2022 , ' Association with HLA-DRβ1 position 37 distinguishes juvenile dermatomyositis from adult-onset myositis ' , Human Molecular Genetics , vol. 31 , no. 14 , pp. 2471-2481 . https://doi.org/10.1093/hmg/ddac019

مصطلحات موضوعية: Adult, Alleles, Amino Acids/genetics, Child, Dermatomyositis/diagnosis, Genetic Predisposition to Disease, HLA-C Antigens/genetics, HLA-DRB1 Chains/genetics, Haplotypes/genetics, Humans, Myositis/diagnosis

Relation: https://research.manchester.ac.uk/en/publications/3bd50bcb-3668-4808-b1e7-0bc04b7c50dd

الاتاحة: https://research.manchester.ac.uk/en/publications/3bd50bcb-3668-4808-b1e7-0bc04b7c50dd
https://doi.org/10.1093/hmg/ddac019

المؤلفون: Consortium, Var Goats, Nijman, Isaäc J, Rosen, Benjamin D, Bardou, Philippe, Faraut, Thomas, Cumer, Tristan, Daly, Kevin G, Zheng, Zhuqing, Cai, Yudong, Asadollahpour, Hojjat, Kul, Bengi Çınar, Zhang, Wei-Yi, Guangxin, E, Ayin, A, Baird, Hayley, Bakhtin, Meirat, Bâlteanu, Valentin A, Barfield, Diana, Berger, Beate, Blichfeldt, Thor, Boink, Geert, Bugiwati, Sri R A, Cai, Zexi, Carolan, Sean, Clark, Emily, Cubric-Curik, Vlatka, Dagong, Muhammad I A, Dorji, Tashi, Drew, Louise, Guo, Jiazhong, Hallsson, Jón, Horvat, Simon, Kantanen, Juha, Kawaguchi, Fuki, Kazymbet, Polat, Khayatzadeh, Negar, Kim, Namshin, Shah, Manoj Kumar, Liao, Yuying, Martínez, Amparo, Masangkay, Joseph S, Masaoka, Maho, Mazza, Raffaele, McEwan, John, Milanesi, Marco, Faruque, Md Omar, Nomura, Yuto, Ouchene-Khelifi, Nadjet-Amina, Pereira, Filipe, Sahana, Goutam, Salavati, Mazdak, Sasazaki, Shinji, Da Silva, Anne, Simčič, Mojca, Sölkner, Johann, Sutherland, Alison, Tigchelaar, Johannes, Zhang, Hongpin, Consortium, Econogene, Ajmone-Marsan, Paolo, Bradley, Daniel G, Colli, Licia, Drögemüller, Cord, Jiang, Yu, Lei, Chuzhao, Mannen, Hideyuki, Pompanon, François, Tosser-Klopp, Gwenola, Lenstra, Johannes A

المصدر: Consortium , V G , Nijman , I J , Rosen , B D , Bardou , P , Faraut , T , Cumer , T , Daly , K G , Zheng , Z , Cai , Y , Asadollahpour , H , Kul , B Ç , Zhang , W-Y , Guangxin , E , Ayin , A , Baird , H , Bakhtin , M , Bâlteanu , V A , Barfield , D , Berger , B , Blichfeldt , T , Boink , G , Bugiwati , S R A , Cai , Z ....

مصطلحات موضوعية: Y-chromosome, domestication, goat, haplogroup, introgression, migration, phylogeography, NETWORKS, MITOCHONDRIAL-DNA, FLOW, GENETIC DIVERSITY, ORIGINS, DIFFERENTIATION, BREEDS, DNA, Mitochondrial/genetics, Goats/genetics, Phylogeny, Haplotypes/genetics, Genetic Variation, Animals, Y Chromosome/genetics

الاتاحة: https://pure.au.dk/portal/en/publications/588fb657-a6e3-42a0-938d-7981ecd25a87
https://doi.org/10.1111/mec.16579

المؤلفون: Halldorsson, Bjarni V., Eggertsson, Hannes P., Moore, Kristjan H.S., Hauswedell, Hannes, Eiriksson, Ogmundur, Ulfarsson, Magnus O., Palsson, Gunnar, Hardarson, Marteinn T., Oddsson, Asmundur, Jensson, Brynjar O., Kristmundsdottir, Snaedis, Sigurpalsdottir, Brynja D., Stefansson, Olafur A., Beyter, Doruk, Holley, Guillaume, Tragante, Vinicius, Gylfason, Arnaldur, Olason, Pall I., Zink, Florian, Asgeirsdottir, Margret, Sverrisson, Sverrir T., Sigurdsson, Brynjar, Gudjonsson, Sigurjon A., Sigurdsson, Gunnar T., Halldorsson, Gisli H., Sveinbjornsson, Gardar, Norland, Kristjan, Styrkarsdottir, Unnur, Magnusdottir, Droplaug N., Snorradottir, Steinunn, Kristinsson, Kari, Sobech, Emilia, Jonsson, Helgi, Geirsson, Arni J., Olafsson, Isleifur, Jonsson, Palmi, Pedersen, Ole Birger, Erikstrup, Christian, Brunak, Søren, Ostrowski, Sisse Rye, Thorleifsson, Gudmar, Jonsson, Frosti, Melsted, Pall, Jonsdottir, Ingileif, Rafnar, Thorunn, Holm, Hilma, Stefansson, Hreinn, Saemundsdottir, Jona, Gudbjartsson, Daniel, Magnusson, Olafur T, Masson, Gisli, Thorsteinsdottir, Unnur, Helgason, Agnar, Jonsson, Hakon, Sulem, Patrick, Stefansson, Kari, Mikkelsen, Susan, Nyegaard, Mette

المصدر: Halldorsson , B V , Eggertsson , H P , Moore , K H S , Hauswedell , H , Eiriksson , O , Ulfarsson , M O , Palsson , G , Hardarson , M T , Oddsson , A , Jensson , B O , Kristmundsdottir , S , Sigurpalsdottir , B D , Stefansson , O A , Beyter , D , Holley , G , Tragante , V , Gylfason , A , Olason , P I , Zink , F , Asgeirsdottir , M , Sverrisson , S T , Sigurdsson , B , ....

مصطلحات موضوعية: Africa/ethnology, Asia/ethnology, Biological Specimen Banks, Cohort Studies, Conserved Sequence, Databases, Genetic, Exons/genetics, Genetic Variation, Genome, Human/genetics, Genomics, Haplotypes/genetics, Humans, INDEL Mutation, Ireland/ethnology, Microsatellite Repeats, Polymorphism, Single Nucleotide/genetics, United Kingdom, Whole Genome Sequencing

وصف الملف: application/pdf

الاتاحة: https://pure.au.dk/portal/en/publications/c60a1140-9a44-48cb-beb3-b643716755de
https://doi.org/10.1038/s41586-022-04965-x
https://pure.au.dk/ws/files/331213846/s41586_022_04965_x.pdf
http://www.scopus.com/inward/record.url?scp=85134541905&partnerID=8YFLogxK

المؤلفون: Goodin, Douglas, Khankhanian, Pouya, Gourraud, Pierre-Antoine, Vince, Nicolas

المساهمون: University of California San Francisco (UC San Francisco), University of California (UC), University of Pennsylvania, Institut de Transplantation et de Recherche en Transplantation CHU Nantes (ITERT), Centre Hospitalier Universitaire de Nantes = Nantes University Hospital (CHU Nantes), Centre de Recherche en Transplantation et Immunologie (U1064 Inserm - CRTI), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)

المصدر: ISSN: 1932-6203.

مصطلحات موضوعية: MESH: Adult, MESH: Alleles, MESH: Multiple Sclerosis / epidemiology, MESH: Multiple Sclerosis / genetics, MESH: Environment, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: HLA-DRB1 Chains / genetics, MESH: Haplotypes / genetics, MESH: Humans, MESH: Male, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/33750973; PUBMED: 33750973; PUBMEDCENTRAL: PMC7984655

الاتاحة: https://inserm.hal.science/inserm-04346737
https://inserm.hal.science/inserm-04346737v2/document
https://inserm.hal.science/inserm-04346737v2/file/journal.pone.0246157.pdf
https://doi.org/10.1371/journal.pone.0246157

المؤلفون: Goodin, Douglas, Oksenberg, Jorge, Douillard, Venceslas, Gourraud, Pierre-Antoine, Vince, Nicolas

المساهمون: University of California San Francisco (UC San Francisco), University of California (UC), Centre de Recherche en Transplantation et Immunologie (U1064 Inserm - CRTI), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)

المصدر: ISSN: 1932-6203.

مصطلحات موضوعية: MESH: Black or African American / genetics, MESH: Case-Control Studies, MESH: Odds Ratio, MESH: White People / genetics, MESH: Gene Frequency / genetics, MESH: Genetic Predisposition to Disease, MESH: HLA-DQ beta-Chains / genetics, MESH: HLA-DRB1 Chains / genetics, MESH: Haplotypes / genetics, MESH: Humans, MESH: Multiple Sclerosis / genetics, [SDV]Life Sciences [q-bio]

Relation: info:eu-repo/semantics/altIdentifier/pmid/34370753; PUBMED: 34370753; PUBMEDCENTRAL: PMC8352072

الاتاحة: https://inserm.hal.science/inserm-04276889
https://inserm.hal.science/inserm-04276889v1/document
https://inserm.hal.science/inserm-04276889v1/file/journal.pone.0254945.pdf
https://doi.org/10.1371/journal.pone.0254945

المؤلفون: Luo, Y., Kanai, M., Choi, W., Li, X., Sakaue, S., Yamamoto, K., Ogawa, K., Gutierrez-Arcelus, M., Gregersen, P.K., Stuart, P.E., Elder, J.T., Forer, L., Schönherr, S., Fuchsberger, C., Smith, A.V., Fellay, J., Carrington, M., Haas, D.W., Guo, X., Palmer, N.D., Chen, Y.I., Rotter, J.I., Taylor, K.D., Rich, S.S., Correa, A., Wilson, J.G., Kathiresan, S., Cho, M.H., Metspalu, A., Esko, T., Okada, Y., Han, B., McLaren, P.J., Raychaudhuri, S.

المساهمون: NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Abe, N., Abecasis, G., Aguet, F., Albert, C., Almasy, L., Alonso, A., Ament, S., Anderson, P., Anugu, P., Applebaum-Bowden, D., Ardlie, K., Dan Arking, X., Arnett, D.K., Ashley-Koch, A., Aslibekyan, S., Assimes, T., Auer, P., Avramopoulos, D., Ayas, N., Balasubramanian, A., Barnard, J., Barnes, K., Barr, R.G., Barron-Casella, E., Barwick, L., Beaty, T., Beck, G., Becker, D., Becker, L., Beer, R., Beitelshees, A., Benjamin, E., Benos, T., Bezerra, M., Bielak, L., Bis, J., Blackwell, T., Blangero, J., Boerwinkle, E., Bowden, D.W., Bowler, R., Brody, J., Broeckel, U., Broome, J., Brown, D., Bunting, K., Burchard, E., Bustamante, C., Buth, E., Cade, B., Cardwell, J., Carey, V., Carrier, J., Carty, C., Casaburi, R., Romero, JPC, Casella, J., Castaldi, P., Chaffin, M., Chang, C., Chang, Y.C., Chasman, D., Chavan, S., Chen, B.J., Chen, W.M., Choi, S.H., Chuang, L.M., Chung, M., Chung, R.H., Clish, C., Comhair, S., Conomos, M., Cornell, E., Crandall, C., Crapo, J., Cupples, L.A., Curran, J., Curtis, J., Custer, B., Damcott, C., Darbar, D., David, S., Davis, C., Daya, M., de Andrade, M., Fuentes, L.L., de Vries, P., DeBaun, M., Deka, R., DeMeo, D., Devine, S., Dinh, H., Doddapaneni, H., Duan, Q., Dugan-Perez, S., Duggirala, R., Durda, J.P., Dutcher, S.K., Eaton, C.

المصدر: Nature genetics, vol. 53, no. 10, pp. 1504-1516

مصطلحات موضوعية: Alleles, Amino Acids/genetics, Gene Frequency/genetics, Genetic Variation, Genetics, Population, HIV Infections/genetics, HIV-1/genetics, HLA Antigens/genetics, Haplotypes/genetics, Host-Pathogen Interactions/genetics, Humans, Linkage Disequilibrium/genetics, Physical Chromosome Mapping, Reference Standards, Selection, Genetic, Viral Load

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/34611364; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_B110F32BA2DA6; https://serval.unil.ch/notice/serval:BIB_B110F32BA2DA; https://serval.unil.ch/resource/serval:BIB_B110F32BA2DA.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_B110F32BA2DA
https://doi.org/10.1038/s41588-021-00935-7
https://serval.unil.ch/resource/serval:BIB_B110F32BA2DA.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_B110F32BA2DA6

المؤلفون: Rogenhofer, Nina, Markoff, Arseni, Ennerst, Xenia, Bogdanova, Nadja, Thaler, Christian

المصدر: http://lobid.org/resources/99370672818306441#!, 38(1):235-242.

مصطلحات موضوعية: Pre-Eclampsia/pathology [MeSH], Heterozygote [MeSH], Reproductive Techniques, Assisted/trends [MeSH], Risk Factors [MeSH], Embryo Transfer/statistics, Annexin A5/genetics [MeSH], Male [MeSH], Genetics, M2 Haplotype, Abortion, Habitual/pathology [MeSH], Placenta/metabolism [MeSH], Annexin, Genetic Predisposition to Disease [MeSH], Premature Birth/genetics [MeSH], Female [MeSH], Habitual/genetics [MeSH], Habitual/epidemiology [MeSH], Adult [MeSH], Humans [MeSH], Premature Birth/pathology [MeSH], Recurrent implantation failure, Pre-Eclampsia/epidemiology [MeSH], Placenta/pathology [MeSH], Young Adult [MeSH], Haplotypes/genetics [MeSH], Blastocyst/pathology [MeSH], Blastocyst/metabolism [MeSH], Pregnancy [MeSH]

Relation: https://repository.publisso.de/resource/frl:6466506; https://doi.org/10.1007/s10815-020-01978-1; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822994/

الاتاحة: https://repository.publisso.de/resource/frl:6466506
https://doi.org/10.1007/s10815-020-01978-1
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7822994/

المؤلفون: Rubinacci, S., Delaneau, O., Marchini, J.

المصدر: PLoS genetics, vol. 16, no. 11, pp. e1009049

مصطلحات موضوعية: Alleles, Computational Biology/methods, Forecasting/methods, Gene Frequency/genetics, Genome-Wide Association Study/methods, Genotype, Haplotypes/genetics, Humans, Models, Theoretical, Polymorphism, Single Nucleotide/genetics

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/33196638; info:eu-repo/semantics/altIdentifier/eissn/1553-7404; info:eu-repo/grantAgreement/ERC//617306///; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_89CBA5F9A38B9; https://serval.unil.ch/notice/serval:BIB_89CBA5F9A38B; https://doi.org/10.1101/797944; https://serval.unil.ch/resource/serval:BIB_89CBA5F9A38B.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_89CBA5F9A38B
https://doi.org/10.1371/journal.pgen.1009049
https://doi.org/10.1101/797944
https://serval.unil.ch/resource/serval:BIB_89CBA5F9A38B.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_89CBA5F9A38B9

المؤلفون: Font-Porterias, N, Arauna, LR, Poveda, A, Bianco, E, Rebato, E, Prata, MJ, Calafell, F, Comas, D

المساهمون: Instituto de Investigação e Inovação em Saúde

مصطلحات موضوعية: Asian Continental Ancestry Group / genetics, Ethnic Groups / genetics, European Continental Ancestry Group / genetics, Founder Effect, Gene Flow / genetics, Genetic Variation / genetics, Genetics, Population, Haplotypes / genetics, Human Migration, Humans, Minority Groups, Roma / genetics

وصف الملف: application/pdf

Relation: PLoS Genetics, vol.15(9):e1008417; https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1008417; https://hdl.handle.net/10216/137949

الاتاحة: https://hdl.handle.net/10216/137949
https://doi.org/10.1371/journal.pgen.1008417

المؤلفون: Kuon, Joel-E., Qi, Weihong, Schläpfer, Pascal, Hirsch-Hoffmann, Matthias, von Bieberstein, Philipp Rogalla, Patrignani, Andrea, Poveda, Lucy, Grob, Stefan, Keller, Miyako, Shimizu-Inatsugi, Rie, Grossniklaus, Ueli, Vanderschuren, Hervé, Gruissem, Wilhelm

المصدر: BMC Biology, 17 (1), 75 (2019)

مصطلحات موضوعية: Chromosome Mapping/methods, Disease Resistance/genetics, Disease Susceptibility, Geminiviridae, Genetic Predisposition to Disease, Haplotypes/genetics, Manihot/genetics, Molecular Sequence Annotation, Plant Diseases/genetics, Allelic expression, Cassava genomes, Cassava mosaic disease, Chromosome proximity ligation, Haplotigs, Optical mapping, Transposable elements, Life sciences, Biochemistry, biophysics & molecular biology, Sciences du vivant, Biochimie, biophysique & biologie moléculaire

Relation: urn:issn:1741-7007; https://orbi.uliege.be/handle/2268/249502; info:hdl:2268/249502; https://orbi.uliege.be/bitstream/2268/249502/1/kuonetal2019.pdf; info:pmid:31533702

الاتاحة: https://orbi.uliege.be/handle/2268/249502
https://orbi.uliege.be/bitstream/2268/249502/1/kuonetal2019.pdf
https://doi.org/10.1186/s12915-019-0697-6

المؤلفون: Kunkle, Brian W, Grenier-Boley, Benjamin, Bellenguez, Céline, Holmes, Clive, Karamujić-Čomić, Hata, Frosch, Matthew P, Thonberg, Hakan, Maier, Wolfgang, Roshchupkin, Gennady, Ghetti, Bernardino, Giedraitis, Vilmantas, Kawalia, Amit, Li, Shuo, Frizatti, Aura, Huebinger, Ryan M, Kilander, Lena, Moebus, Susanne, Hernández, Isabel, Kamboh, M Ilyas, Brundin, RoseMarie, Turton, James, Yang, Qiong, Katz, Mindy J, Concari, Letizia, Chouraki, Vincent, Lord, Jenny, Beiser, Alexa S, Keene, C Dirk, Helisalmi, Seppo, Kloszewska, Iwona, Kukull, Walter A, Koivisto, Anne Maria, Lynch, Aoibhinn, Tarraga, Lluís, Larson, Eric B, Martin, Eden R, Haapasalo, Annakaisa, Lawlor, Brian, Mosley, Thomas H, Lipton, Richard B, Solfrizzi, Vincenzo, Gill, Michael, Longstreth, W. T., Montine, Thomas J, Frisardi, Vincenza, Diez-Fairen, Monica, Sleegers, Kristel, Rivadeneira, Fernando, Petersen, Ronald C, Deramecourt, Vincent, Alvarez, Ignacio, Salani, Francesca, Ciaramella, Antonio, Boerwinkle, Eric, Reiman, Eric M, Fievet, Nathalie, Rotter, Jerome I, Badarinarayan, Nandini, Reisch, Joan S, Hanon, Olivier, Cupidi, Chiara, Andre Uitterlinden, A. G., Royall, Donald R, Dufouil, Carole, Maletta, Raffaele Giovanni, de Rojas, Itziar, Sano, Mary, Brice, Alexis, Jakobsdottir, Johanna, Cecchetti, Roberta, George-Hyslop, Peter St, Ritchie, Karen, Tsolaki, Magda, Tsuang, Debby W, Dubois, Bruno, Craig, David, Wu, Chuang-Kuo, Soininen, Hilkka, Avramidou, Despoina, Hamilton-Nelson, Kara L, Albin, Roger L, Fratiglioni, Laura, Germanou, Antonia, Apostolova, Liana G, Keller, Lina, Koutroumani, Maria, Arnold, Steven E, Panza, Francesco, Gkatzima, Olymbia, Asthana, Sanjay, Moreno-Grau, Sonia, Hannequin, Didier, Whitehead, Patrice, Atwood, Craig S, Caffarra, Paolo, Hampel, Harald, Quintela, Inés, Carracedo, Ángel, Lannfelt, Lars, Rubinsztein, David C, Barnes, Lisa L, Olaso, Robert, Pasquier, Florence, Frölich, Lutz, Barral, Sandra, McGuinness, Bernadette, Beach, Thomas G, Johnston, Janet A, Becker, James T, Passmore, Peter, Bigio, Eileen H, Schott, Jonathan M, Sims, Rebecca, Raybould, Rachel, Bird, Thomas D, Warren, Jason D, Boeve, Bradley F, Lupton, Michelle K, Bowen, James D, Proitsi, Petra, Boxer, Adam, Powell, John F, Burke, James R, Kauwe, John S K, Chen, Yuning, Burns, Jeffrey M, Mancuso, Michelangelo, Buxbaum, Joseph D, Bonuccelli, Ubaldo, Cairns, Nigel J, McQuillin, Andrew, Cao, Chuanhai, Livingston, Gill, Carlson, Chris S, Bass, Nicholas J, Kuzma, Amanda B, Carlsson, Cynthia M, Hardy, John, Carney, Regina M, Bras, Jose, Carrasquillo, Minerva M, Guerreiro, Rita, Allen, Mariet, Chui, Helena C, Fisher, Elizabeth, Masullo, Carlo, Hiltunen, Mikko, Crocco, Elizabeth A, DeCarli, Charles, Bisceglio, Gina, Dick, Malcolm, Ma, Li, Duara, Ranjan, Graff-Radford, Neill R, Evans, Denis A, Hodges, Angela, Faber, Kelley M, Morgan, Taniesha, Scherer, Martin, Fallon, Kenneth B, Riemenschneider, Matthias, Fardo, David W, Heun, Reinhard, Farlow, Martin R, Kölsch, Heike, Ferris, Steven, Leber, Markus, Foroud, Tatiana M, Ahmad, Shahzad, Heuser, Isabella, Galasko, Douglas R, Giegling, Ina, Gearing, Marla, Hüll, Michael, Geschwind, Daniel H, Gilbert, John R, Morris, John, Green, Robert C, Mayo, Kevin, Vardarajan, Badri N, Growdon, John H, Feulner, Thomas, Hamilton, Ronald L, Harrell, Lindy E, Drichel, Dmitriy, Honig, Lawrence S, Cushion, Thomas D, Huentelman, Matthew J, Hollingworth, Paul, Hulette, Christine M, Epelbaum, Jacques, Hyman, Bradley T, Marshall, Rachel, Jarvik, Gail P, Meggy, Alun, Abner, Erin, Menzies, Georgina E, Jin, Lee-Way, Leonenko, Ganna, Real, Luis M, Jun, Gyungah R, Hoffmann, Per, Baldwin, Clinton T, Grozeva, Detelina, Karydas, Anna, Russo, Giancarlo, Kaye, Jeffrey A, Kim, Ronald, Jessen, Frank, Kowall, Neil W, Vellas, Bruno, Kramer, Joel H, Boada, Merce, Vardy, Emma, LaFerla, Frank M, Jöckel, Karl-Heinz, Lah, James J, Dichgans, Martin, Leverenz, James B, Mann, David, Levey, Allan I, Pickering-Brown, Stuart, Lieberman, Andrew P, Bis, Joshua C, Beecham, Gary W, Klopp, Norman, Lunetta, Kathryn L, Wichmann, H-Erich, Lyketsos, Constantine G, Morgan, Kevin, Marson, Daniel C, Brown, Kristelle, Martiniuk, Frank, Medway, Christopher, Mash, Deborah C, Garnier, Jean-Guillaume, Nöthen, Markus M, Masliah, Eliezer, Hooper, Nigel M, McCormick, Wayne C, Daniele, Antonio, McCurry, Susan M, Bayer, Anthony, McDavid, Andrew N, Gallacher, John, McKee, Ann C, Harold, Denise, van den Bussche, Hendrik, Mesulam, Marsel, Brayne, Carol, Miller, Bruce L, Riedel-Heller, Steffi, Miller, Carol A, Miller, Joshua W, Al-Chalabi, Ammar, Morris, John C, Shaw, Christopher E, Fitzpatrick, Annette L, Myers, Amanda J, Wiltfang, Jens, O'Bryant, Sid, Olichney, John M, Alvarez, Victoria, Parisi, Joseph E, Singleton, Andrew B, Paulson, Henry L, Collinge, John, Perry, William R, Valladares, Otto, Mead, Simon, Peskind, Elaine, Cribbs, David H, Rossor, Martin, Pierce, Aimee, Ryan, Natalie S, Poon, Wayne W, Nacmias, Benedetta, Potter, Huntington, Sorbi, Sandro, Moutet, Marie-Laure, Quinn, Joseph F, Sacchinelli, Eleonora, Raj, Ashok, Spalletta, Gianfranco, Raskind, Murray, Caltagirone, Carlo, Bossù, Paola, Orfei, Maria Donata, Reisberg, Barry, Clarke, Robert, Gerrish, Amy, Reitz, Christiane, Smith, A David, Ringman, John M, Warden, Donald, Roberson, Erik D, Wilcock, Gordon, Rogaeva, Ekaterina, Bruni, Amalia Cecilia, Rosen, Howard J, Gallo, Maura, Smith, Albert V, Rosenberg, Roger N, Ben-Shlomo, Yoav, Sager, Mark A, Mecocci, Patrizia, Saykin, Andrew J, Pastor, Pau, Cuccaro, Michael L, Vance, Jeffery M, Schneider, Julie A, Schneider, Lori S, Qu, Liming, Slifer, Susan, Seeley, William W, Smith, Amanda G, Sonnen, Joshua A, Spina, Salvatore, Stern, Robert A, Swerdlow, Russell H, Tang, Mitchell, Tanzi, Rudolph E, Trojanowski, John Q, Bacq, Delphine, Troncoso, Juan C, Van Deerlin, Vivianna M, Van Eldik, Linda J, Vinters, Harry V, Vonsattel, Jean Paul, Weintraub, Sandra, Welsh-Bohmer, Kathleen A, Wilhelmsen, Kirk C, Williamson, Jennifer, Wingo, Thomas S, Damotte, Vincent, Denning, Nicola, Woltjer, Randall L, Wright, Clinton B, Yu, Chang-En, Yu, Lei, Saba, Yasaman, Pilotto, Alberto, Bullido, Maria J, Peters, Oliver, Crane, Paul K, Bennett, David, Jian, Xueqiu, Bosco, Paola, Coto, Eliecer, Boccardi, Virginia, De Jager, Phil L, Lleo, Alberto, Warner, Nick, Lopez, Oscar L, Ingelsson, Martin, Deloukas, Panagiotis, Cruchaga, Carlos, Zhao, Yi, Graff, Caroline, Gwilliam, Rhian, Fornage, Myriam, Goate, Alison M, Sanchez-Juan, Pascual, Kehoe, Patrick G, Amin, Najaf, Ertekin-Taner, Nilifur, Berr, Claudine, Debette, Stéphanie, Del Zompo, Maria, Love, Seth, Launer, Lenore J, Younkin, Steven G, Dartigues, Jean-Francois, Corcoran, Chris, Ikram, M Arfan, Dickson, Dennis W, Nicolas, Gael, Campion, Dominique, Tschanz, JoAnn, Fox, Nick C, Schmidt, Helena, Hakonarson, Hakon, Clarimon, Jordi, Munger, Ron, Schmidt, Reinhold, Farrer, Lindsay A, Van Broeckhoven, Christine, C O'Donovan, Michael, DeStefano, Anita L, Jones, Lesley, Choi, Seung-Hoan, Haines, Jonathan L, Deleuze, Jean-Francois, Owen, Michael J, Gudnason, Vilmundur, Mayeux, Richard, Escott-Price, Valentina, Psaty, Bruce M, Ramirez, Alfredo, Wang, Li-San, Ruiz, Agustin, Mateo, Ignacio, van Duijn, Cornelia M, Holmans, Peter A, Seshadri, Sudha, Williams, Julie, Amouyel, Phillippe, Schellenberg, Gerard D, Lambert, Jean-Charles, Pericak-Vance, Margaret A, Consortium, Alzheimer Disease Genetics, Initiative, European Alzheimer’s Disease, Hughes, Joseph T, Consortium, Cohorts for Heart and Aging Research in Genomic Epidemiology, Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium, Adams, Hieab H, Malamon, John, Naj, Adam C, Sanchez-Garcia, Florentino, Patel, Yogen, Brody, Jennifer A, Dombroski, Beth A, Naranjo, Maria Candida Deniz, Daniilidou, Makrina, Eiriksdottir, Gudny, Mukherjee, Shubhabrata, Wallon, David, Uphill, James, Boland, Anne, Aspelund, Thor, Cantwell, Laura B, Garzia, Fabienne, Galimberti, Daniela, Hofer, Edith, Butkiewicz, Mariusz, Fin, Bertrand, Scarpini, Elio, Sarnowski, Chloe, Bush, Will S, Vronskaya, Maria, Meslage, Stéphane, Kornhuber, Johannes, White, Charles C, Song, Yuenjoo, Barber, Robert C, Engelborghs, Sebastiaan, Sordon, Sabrina, Voijnovic, Dina, Adams, Perrie M, Vandenberghe, Rik, van der Lee, Sven J, Mayhaus, Manuel, Cupples, L Adrienne, Albert, Marilyn S, De Deyn, Peter P, Gu, Wei, Himali, Jayanadra J, Beekly, Duane, Squassina, Alessio, Hartmann, Annette M, Orellana, Adelina, Amlie-Wolf, Alexandre, Blacker, Deborah, Rodriguez-Rodriguez, Eloy, Lovestone, Simon, Garcia, Melissa E, Doody, Rachelle S, Munoz-Fernadez, Carmen, Sussams, Rebecca, Lin, Honghuang, Fairchild, Thomas J, Benito, Yolanda A

المصدر: Nature genetics 51(3), 414-430 (2019). doi:10.1038/s41588-019-0358-2

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Aged, Alzheimer Disease: genetics, Amyloid beta-Peptides: genetics, Case-Control Studies, Female, Genetic Loci: genetics, Genetic Predisposition to Disease: genetics, Genetic Testing: methods, Genome-Wide Association Study: methods, Haplotypes: genetics, Humans, Immunity: genetics, Lipid Metabolism: genetics, Lipids: genetics, Male, tau Proteins: genetics, Amyloid beta-Peptides, Lipids, tau Proteins

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/1546-1718; info:eu-repo/semantics/altIdentifier/pmid/pmid:30820047; info:eu-repo/semantics/altIdentifier/issn/1061-4036; https://pub.dzne.de/record/140528; https://pub.dzne.de/search?p=id:%22DZNE-2020-06850%22

الاتاحة: https://pub.dzne.de/record/140528
https://pub.dzne.de/search?p=id:%22DZNE-2020-06850%22

المؤلفون: Posthuma, Danielle

المصدر: Posthuma , D & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018 , ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ' , American Journal of Human Genetics , vol. 102 , no. 6 , pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021

مصطلحات موضوعية: Adult, Body Height/genetics, Computer Simulation, Databases, Genetic, Genome, Human, Genotype, Haplotypes/genetics, Humans, Inheritance Patterns/genetics, Likelihood Functions, Linkage Disequilibrium/genetics, Phenotype, Polymorphism, Single Nucleotide/genetics, Regression Analysis, Schizophrenia/genetics, accuracy, schizophrenia, biasedness, genome-wide SNPs, linkage disequilibrium score regression, genetic correlation, height, body mass index, SNP heritability, genomic restricted maximum likelihood

وصف الملف: application/pdf

الاتاحة: https://research.vu.nl/en/publications/41ee56a1-47fc-4e4b-9ee2-d91677643fd8
https://doi.org/10.1016/j.ajhg.2018.03.021
https://hdl.handle.net/1871.1/41ee56a1-47fc-4e4b-9ee2-d91677643fd8
https://research.vu.nl/ws/files/83592932/Estimation_of_Genetic_Correlation_via_Linkage_Disequilibrium_Score_Regression_and_Genomic_Restricted_Maximum_Likelihood.pdf
http://www.scopus.com/inward/record.url?scp=85046126170&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85046126170&partnerID=8YFLogxK

المؤلفون: Hamdi, Yosr, Ben Rekaya, Mariem, Jingxuan, Shan, Nagara, Majdi, Messaoud, Olfa, Benammar Elgaaied, Amel, Mrad, Ridha, Chouchane, Lotfi, Boubaker, Mohamed Samir, Abdelhak, Sonia, Boussen, Hamouda, Romdhane, Lilia

المساهمون: Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory (LR11IPT05), Université de Tunis El Manar (UTM)-Institut Pasteur de Tunis, Pasteur Network (Réseau International des Instituts Pasteur)-Pasteur Network (Réseau International des Instituts Pasteur), Weill Cornell Medicine Qatar, Faculté des Sciences Mathématiques, Physiques et Naturelles de Tunis (FST), Université de Tunis El Manar (UTM), Hôpital Charles Nicolle Tunis, Hôpital Abderrahmen Mami, Faculté des Sciences de Bizerte Université de Carthage, Université de Carthage (Tunisie) (UCAR), This work was supported by the “Qatar National Research Foundation” (NPRP 08–083–3-031) that contributed to the design of the study, collection, analysis, interpretation of data and in writing the manuscript., The authors would like to thank all the individuals who took part in this study and all the researchers, clinicians, technicians and administrative staff who have enabled this work to be carried out.

المصدر: ISSN: 1471-2407.

مصطلحات موضوعية: Functional analysis, Breast cancer susceptibility, Haplotype analysis, Population genetics, MESH: Adult, MESH: African Continental Ancestry Group/genetics, MESH: Computer Simulation, MESH: Female, MESH: Gene Frequency/genetics, MESH: Genetic Loci/genetics, MESH: Genetic Predisposition to Disease, MESH: Genome-Wide Association Study, MESH: Haplotypes/genetics, MESH: Healthy Volunteers, MESH: Humans, MESH: Linkage Disequilibrium/genetics, MESH: Male, MESH: Middle Aged, MESH: Polymorphism, Single Nucleotide, MESH: Tunisia, MESH: Breast Neoplasms/genetics, [SDV.CAN]Life Sciences [q-bio]/Cancer, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

Relation: info:eu-repo/semantics/altIdentifier/pmid/30594178; PUBMED: 30594178; PUBMEDCENTRAL: PMC6310952

الاتاحة: https://riip.hal.science/pasteur-01984744
https://riip.hal.science/pasteur-01984744v1/document
https://riip.hal.science/pasteur-01984744v1/file/A%20genome.pdf
https://doi.org/10.1186/s12885-018-5133-8

المؤلفون: Pierre Blacher, Ornela De Gasperin, Guglielmo Grasso, Solenn Sarton‐Lohéac, Roxane Allemann, Michel Chapuisat

المصدر: Molecular ecology, vol. 32, no. 5, pp. 1062-1072

مصطلحات موضوعية: Animals, Female, Ants/genetics, Polymorphism, Genetic/genetics, Genotype, Haplotypes/genetics, Reproduction/genetics, Social Behavior, ants, genetic load, inversions, social polymorphism, supergenes, Genetics, Ecology, Evolution, Behavior and Systematics

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae2f68c5748cc57dd4a4376606d2496
https://pubmed.ncbi.nlm.nih.gov/36504171