skip to main content
Idioma:
Mostrar Somente
Refinado por: Nome da Publicação: American Journal Of Human Genetics remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and Finding of Significant Linkage to Chromosome 6q22
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and Finding of Significant Linkage to Chromosome 6q22
Material Type:
Artigo 		Adicionar ao Meu Espaço

Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and Finding of Significant Linkage to Chromosome 6q22

Middleton, F.A. ; Pato, M.T. ; Gentile, K.L. ; Morley, C.P. ; Zhao, X. ; Eisener, A.F. ; Brown, A. ; Petryshen, T.L. ; Kirby, A.N. ; Medeiros, H. ; Carvalho, C. ; Macedo, A. ; Dourado, A. ; Coelho, I. ; Valente, J. ; Soares, M.J. ; Ferreira, C.P. ; Lei, M. ; Azevedo, M.H. ; Kennedy, J.L. ; Daly, M.J. ; Sklar, P. ; Pato, C.N.

American journal of human genetics, 2004-05, Vol.74 (5), p.886-897 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

Texto completo disponível

Citações Citado por
2
American Journal of Human Genetics
American Journal of Human Genetics
Material Type:
Artigo 		Adicionar ao Meu Espaço

American Journal of Human Genetics

McQueen, M. B ; Devlin, B ; Faraone, S. V ; Nimgaonkar, V. L ; Sklar, P ; Smoller, J. W ; Abou Jamra, R ; Albus, M ; Bacanu, S. A ; Baron, M ; Barrett, T. B ; Berrettini, W ; Blacker, D ; Byerley, W ; Cichon, S ; Coryell, W ; Craddock, N ; Daly, M. J ; Depaulo, J. R ; Edenberg, H. J ; Foroud, T ; Gill, M ; Gilliam, T. C ; Hamshere, M ; Jones, I ; Jones, L ; Juo, S. H ; Kelsoe, J. R ; Lambert, D ; Lange, C ; Lerer, B ; Liu, J ; Maier, W ; Mackinnon, J. D ; McInnis, M. G ; McMahon, F. J ; Murphy, D. L ; Nothen, M. M ; Nurnberger, J. I ; Pato, C. N ; Pato, M. T ; Potash, J. B ; Propping, P ; Pulver, A. E ; Rice, J. P ; Rietschel, M ; Scheftner, W ; Schumacher, J ; Segurado, R ; Van Steen, Kristel ; Xie, W ; Zandi, P. P ; Laird, N. M

American journal of human genetics, 2005, p.582-95 [Periódico revisado por pares]

University of Chicago Press

Texto completo disponível

Citações Citado por
3
A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder
A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

Duan, Jubao ; Shi, Jianxin ; Fiorentino, Alessia ; Leites, Catherine ; Chen, Xiangning ; Moy, Winton ; Chen, Jingchun ; Alexandrov, Boian S. ; Usheva, Anny ; He, Deli ; Freda, Jessica ; O’Brien, Niamh L. ; Gejman, Pablo V. ; Sanders, Alan R. ; Duan, Jubao ; Levinson, Douglas F. ; Shi, Jianxin ; Buccola, Nancy G. ; Mowry, Bryan J. ; Freedman, Robert ; Olincy, Ann ; Amin, Farooq ; Black, Donald W. ; Silverman, Jeremy M. ; Byerley, William F. ; Svrakic, Dragan M. ; Cloninger, C. Robert ; Pato, Michele T. ; Sobell, Janet L. ; Medeiros, Helena ; Abbott, Colony ; Skar, Brooke ; Buckley, Peter F. ; Bromet, Evelyn J. ; Escamilla, Michael A. ; Fanous, Ayman H. ; Lehrer, Douglas S. ; Macciardi, Fabio ; Malaspina, Dolores ; McCarroll, Steve A. ; Marder, Stephen R. ; Moran, Jennifer ; Morley, Christopher P. ; Nicolini, Humberto ; Perkins, Diana O. ; Purcell, Shaun M. ; Rapaport, Mark H. ; Sklar, Pamela ; Smoller, Jordan W. ; Knowles, James A. ; Pato, Carlos N. ; McQuillin, Andrew ; Sanders, Alan R. ; Gershon, Elliot S. ; DeLisi, Lynn E. ; Bishop, Alan R. ; Gurling, Hugh M.D. ; Pato, Michele T. ; Levinson, Douglas F. ; Kendler, Kenneth S. ; Pato, Carlos N. ; Gejman, Pablo V.

American journal of human genetics, 2014-12, Vol.95 (6), p.744-753 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
4
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Material Type:
Artigo 		Adicionar ao Meu Espaço

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

Gusev, Alexander ; Ripke, Stephan ; Walters, James T.R. ; Agartz, Ingrid ; Albus, Margot ; Bene, Judit ; Bevilacqua, Elizabeth ; Bigdeli, Tim B. ; Bruggeman, Richard ; Buckner, Randy L. ; Carr, Vaughan J. ; Catts, Stanley V. ; Chan, Raymond C.K. ; Cheng, Wei ; Cohen, Nadine ; Curtis, David ; Dikeos, Dimitris ; Dinan, Timothy ; Eriksson, Johan ; Escott-Price, Valentina ; Franke, Lude ; Godard, Stephanie ; Goldstein, Jacqueline I. ; de Haan, Lieuwe ; Hartmann, Annette M. ; Hoffmann, Per ; Hofman, Andrea ; Hollegaard, Mads V. ; Hougaard, David M. ; Ikeda, Masashi ; Kim, Yunjung ; Kucinskas, Vaidutis ; Laurent, Claudine ; Limborska, Svetlana ; Loughland, Carmel M. ; Macek, Milan ; Marsal, Sara ; Mattheisen, Manuel ; Milanova, Vihra ; Mors, Ole ; Mortensen, Preben B. ; Olsen, Line ; Parkhomenko, Elena ; Paunio, Tiina ; Pimm, Jonathan ; Purcell, Shaun M. ; Reichenberg, Abraham ; Reimers, Mark A. ; Richards, Alexander L. ; Roussos, Panos ; Ruderfer, Douglas M. ; Sigurdsson, Engilbert ; Silverman, Jeremy M. ; So, Hon-Cheong ; Spencer, Chris C.A. ; Stefansson, Hreinn ; Straub, Richard E. ; Strengman, Eric ; Strohmaier, Jana ; Svrakic, Dragan M. ; Tosato, Sarah ; Veijola, Juha ; Walsh, Dermot ; Wang, Dai ; Weiser, Mark ; Wolen, Aaron R. ; Wong, Emily H.M. ; Stefansson, Kari ; Andreassen, Ole A. ; Ehrenreich, Hannelore ; Gill, Michael ; Hultman, Christina M. ; Jablensky, Assen V. ; McQuillin, Andrew ; Pato, Carlos N. ; Rietschel, Marcella ; Sham, Pak C. ; Sklar, Pamela ; Weinberger, Daniel R. ; Daly, Mark J. ; Crisponi, Laura ; Figueroa, Jonine ; Gaudet, Mia M. ; Hall, Per ; Hein, Rebecca ; Irwanto, Astrid ; Johansson, Mattias ; Lund, Eiliv ; Peto, Julian ; Rahman, Nazneen ; Southey, Melissa C. ; Travis, Ruth ; Waisfisz, Quinten ; Pato, Carlos ; Stahl, Eli ; Belbin, Gillian ; Kenny, Eimear E. ; Purcell, Shaun ; Chasman, Daniel ; Neale, Benjamin

American journal of human genetics, 2015-10, Vol.97 (4), p.576-592 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
5
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q
Material Type:
Artigo 		Adicionar ao Meu Espaço

Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q

McQueen, Matthew B. ; Devlin, B. ; Faraone, Stephen V. ; Nimgaonkar, Vishwajit L. ; Sklar, Pamela ; Smoller, Jordan W. ; Abou Jamra, Rami ; Albus, Margot ; Bacanu, Silviu-Alin ; Baron, Miron ; Barrett, Thomas B. ; Berrettini, Wade ; Blacker, Deborah ; Byerley, William ; Cichon, Sven ; Coryell, Willam ; Craddock, Nick ; Daly, Mark J. ; DePaulo, J. Raymond ; Edenberg, Howard J. ; Foroud, Tatiana ; Gill, Michael ; Gilliam, T. Conrad ; Hamshere, Marian ; Jones, Ian ; Jones, Lisa ; Juo, Suh-Hang ; Kelsoe, John R. ; Lambert, David ; Lange, Christoph ; Lerer, Bernard ; Liu, Jianjun ; Maier, Wolfgang ; MacKinnon, James D. ; McInnis, Melvin G. ; McMahon, Francis J. ; Murphy, Dennis L. ; Nöthen, Markus M. ; Nurnberger, John I. ; Pato, Carlos N. ; Pato, Michele T. ; Potash, James B. ; Propping, Peter ; Pulver, Ann E. ; Rice, John P. ; Rietschel, Marcella ; Scheftner, William ; Schumacher, Johannes ; Segurado, Ricardo ; Van Steen, Kristel ; Xie, Weiting ; Zandi, Peter P. ; Laird, Nan M.

American journal of human genetics, 2005-10, Vol.77 (4), p.582-595 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

Texto completo disponível

Citações Citado por
6
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Material Type:
Artigo 		Adicionar ao Meu Espaço

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

Trynka, Gosia ; Stahl, Eli ; Neale, Benjamin M. ; Farh, Kai-How ; Pers, Tune H. ; Albus, Margot ; Cahn, Wiepke ; Cai, Guiqing ; Carr, Vaughan J. ; Carrera, Noa ; Cheng, Wei ; Cheung, Eric F.C. ; Cohen, David ; Cormican, Paul ; Craddock, Nick ; Demontis, Ditte ; Djurovic, Srdjan ; Donohoe, Gary ; Dudbridge, Frank ; Durmishi, Naser ; Eriksson, Johan ; Farrell, Martilias S. ; Freimer, Nelson B. ; Fromer, Menachem ; Godard, Stephanie ; Goldstein, Jacqueline I. ; Grove, Jakob ; Hartmann, Annette M. ; Henskens, Frans A. ; Herms, Stefan ; Hirschhorn, Joel N. ; Hoffmann, Per ; Hougaard, David M. ; Ikeda, Masashi ; Julià, Antonio ; Kelly, Brian J. ; Kennedy, James L. ; Kucinskas, Vaidutis ; Kuzelova-Ptackova, Hana ; Laurent, Claudine ; Lee, S. Hong ; Li, Tao ; Lieberman, Jeffrey ; Limborska, Svetlana ; Loughland, Carmel M. ; Lnnqvist, Jouko ; Marsal, Sara ; McCarley, Robert W. ; Meijer, Carin J. ; Melegh, Bela ; Melle, Ingrid ; Milani, Lili ; Mors, Ole ; Myin-Germeys, Inez ; Nikitina-Zake, Liene ; O’Callaghan, Eadbhard ; O’Dushlaine, Colm ; O’Neill, F. Anthony ; Oh, Sang-Yun ; Pantelis, Christos ; Parkhomenko, Elena ; Perkins, Diana O. ; Powell, John ; Quested, Digby ; Salomaa, Veikko ; Schubert, Christian R. ; Shi, Jianxin ; Sigurdsson, Engilbert ; Sim, Kang ; Stogmann, Elisabeth ; Strengman, Eric ; Suvisaari, Jaana ; Thirumalai, Srinivas ; Veijola, Juha ; Walsh, Dermot ; Weiser, Mark ; Witt, Stephanie H. ; Wong, Emily H.M. ; Wu, Jing Qin ; Stefansson, Kari ; Blackwood, Douglas H.R. ; Ehrenreich, Hannelore ; Gurling, Hugh ; Hultman, Christina M. ; Kirov, George ; Malhotra, Anil K. ; McCarroll, Steven A. ; McQuillin, Andrew ; Palotie, Aarno ; Rietschel, Marcella ; Sham, Pak C. ; O’Donovan, Michael C. ; Bergen, Sarah ; Magnusson, Patrik K.E. ; Scolnick, Edward ; Purcell, Shaun M. ; Pasaniuc, Bogdan ; Sullivan, Patrick F. ; Raychaudhuri, Soumya ; Price, Alkes L.

American journal of human genetics, 2014-11, Vol.95 (5), p.535-552 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
7
Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing
Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing
Material Type:
Artigo 		Adicionar ao Meu Espaço

Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing

Hanks, Sarah C. ; Forer, Lukas ; Schönherr, Sebastian ; LeFaive, Jonathon ; Martins, Taylor ; Welch, Ryan ; Gagliano Taliun, Sarah A. ; Braff, David ; Johnsen, Jill M. ; Kenny, Eimear E. ; Konkle, Barbara A. ; Laakso, Markku ; Loos, Ruth F.J. ; McCarroll, Steven ; Pato, Carlos ; Pato, Michele T. ; Smith, Albert V. ; Boehnke, Michael ; Scott, Laura J. ; Fuchsberger, Christian

American journal of human genetics, 2022-09, Vol.109 (9), p.1653-1666 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
8
Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors
Material Type:
Artigo 		Adicionar ao Meu Espaço

Improved Detection of Common Variants Associated with Schizophrenia by Leveraging Pleiotropy with Cardiovascular-Disease Risk Factors

Andreassen, Ole A. ; Djurovic, Srdjan ; Thompson, Wesley K. ; Schork, Andrew J. ; Kendler, Kenneth S. ; O’Donovan, Michael C. ; Rujescu, Dan ; Werge, Thomas ; van de Bunt, Martijn ; Morris, Andrew P. ; McCarthy, Mark I. ; Roddey, J. Cooper ; McEvoy, Linda K. ; Desikan, Rahul S. ; Dale, Anders M.

American journal of human genetics, 2013-02, Vol.92 (2), p.197-209 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
9
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
Material Type:
Artigo 		Adicionar ao Meu Espaço

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Moser, Gerhard ; Agartz, Ingrid ; Andreassen, Ole A. ; Anjorin, Adebayo ; Bass, Nicholas ; Bergen, Sarah E. ; Betancur, Catalina ; Black, Donald W. ; Bloss, Cinnamon S. ; Buxbaum, Joseph D. ; Cantor, Rita M. ; Cormand, Bru ; Coryell, William H. ; Craig, Ian W. ; Crosbie, Jennifer ; Djurovic, Srdjan ; Ebstein, Richard P. ; Etain, Bruno ; Faraone, Stephen V. ; Farmer, Anne E. ; Ferrier, I. Nicol ; Fombonne, Eric ; Frank, Josef ; Franke, Barbara ; Freitag, Christine M. ; Friedl, Marion ; Gershon, Elliot S. ; Gill, Michael ; Gordon, Scott D. ; Green, Elaine K. ; De Haan, Lieuwe ; Haines, Jonathan L. ; Hakonarson, Hakon ; Hallmayer, Joachim ; Hamilton, Steven P. ; Hamshere, Marian L. ; Hoogendijk, Witte J. ; Hottenga, Jouke-Jan ; Hus, Vanessa ; Jamain, Stéphane ; Jones, Lisa ; Kenny, Elaine ; Krabbendam, Lydia ; Kuntsi, Jonna ; Landén, Mikael ; Lesch, Klaus-Peter ; Lichtenstein, Paul ; Lieberman, Jeffrey A. ; Linszen, Don H. ; Loo, Sandra K. ; Lowe, Jennifer K. ; Lucae, Susanne ; Magnusson, Patrik K.E. ; Mahon, Pamela B. ; Martin, Christa L. ; McGhee, Kevin A. ; McGuffin, Peter ; McInnis, Melvin G. ; McIntosh, Andrew ; McLean, Alan W. ; McMahon, William M. ; Meier, Sandra ; Meng, Fan ; Meyer, Jobst ; Middeldorp, Christel M. ; Miranda, Ana ; Montgomery, Grant W. ; Mühleisen, Thomas W. ; Neale, Benjamin M. ; Nyholt, Dale R. ; O’Donovan, Michael C. ; Olsen, Line ; Penninx, Brenda W. ; Pergadia, Michele L. ; Pericak-Vance, Margaret A. ; Perlis, Roy H. ; Posthuma, Danielle ; Rasmussen, Henrik B. ; Reif, Andreas ; Ribasés, Marta ; Rice, John P. ; Rossin, Lizzy ; Sanders, Stephan J. ; Schachar, Russell ; Schellenberg, Gerard D. ; Schumacher, Johannes ; Scott, Laura J. ; Smalley, Susan L. ; Smit, Johannes H. ; Szelinger, Szabocls ; Thapar, Anita ; Thirumalai, Srinivasa ; Treutlein, Jens ; Visscher, Peter M. ; Willemsen, Gonneke ; Young, Allan H. ; Zammit, Stanley ; Zitman, Frans G. ; Potash, James B. ; Shi, Jianxin

American journal of human genetics, 2015-02, Vol.96 (2), p.283-294 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por
10
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals
Material Type:
Artigo 		Adicionar ao Meu Espaço

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Howrigan, Daniel P. ; Abbott, Liam E. ; Tashman, Katherine ; Singh, Tarjinder ; Watts, Nick ; Lal, Dennis ; Hakonarson, Hakon ; Weckhuysen, Sarah ; Petrovski, Slavé ; Cossette, Patrick ; Cotsapas, Chris ; De Jonghe, Peter ; Guerrini, Renzo ; Marson, Anthony G. ; Depondt, Chantal ; Striano, Pasquale ; Freyer, Catharine ; Regan, Brigid M. ; Leu, Costin ; Johns, Esther M.C. ; Macdonald, Alexandra ; Bahlo, Melanie ; Todaro, Marian ; Stamberger, Hannah ; Sadoway, Tara R. ; Kousiappa, Ioanna ; Tanteles, George A. ; Štěrbová, Katalin ; Kunz, Wolfram S. ; Zsurka, Gábor ; Elger, Christian E. ; Rademacher, Michael ; van Baalen, Andreas ; von Spiczak, Sarah ; Afawi, Zaid ; Canavati, Christina ; Kluger, Gerhard ; Blatt, Ilan ; Weber, Yvonne G. ; Wolking, Stefan ; Rau, Sarah ; Steinhoff, Bernhard J. ; Schulze-Bonhage, Andreas ; Borggräfe, Ingo ; Madeleyn, Rene ; Kälviäinen, Reetta ; Linnankivi, Tarja ; Chung, Seo-Kyung ; Balestrini, Simona ; Braatz, Vera ; Johnson, Michael R. ; Auce, Pauls ; Sham, Pak C. ; Lui, Colin H.T. ; Doherty, Colin P. ; Shukralla, Arif ; El-Naggar, Hany ; Vari, Maria Stella ; Salpietro, Vincenzo ; Tinuper, Paolo ; Gagliardi, Monica ; Montomoli, Martino ; Doccini, Viola ; Inoue, Yushi ; Yamakawa, Kazuhiro ; Tumiene, Birute ; Sadleir, Lynette G. ; Caglayan, S. Hande ; Arslan, Mutluay ; Yis, Uluc ; Topaloglu, Pınar ; Baykan, Betül ; Salman, Barış ; Haryanyan, Garen ; Özkara, Çiğdem ; Poduri, Annapurna ; Shiedley, Beth R. ; Shain, Catherine ; French, Jacqueline A. ; Kuzniecky, Ruben I. ; Hegde, Manu ; Helbig, Katherine L. ; Piras, Federica ; Reif, Andreas ; McQuillin, Andrew ; Johnstone, Mandy ; Palotie, Aarno ; Carvalho, Celia Barreto ; Achtyes, Eric D. ; Azevedo, Maria Helena ; Kotov, Roman ; Lehrer, Douglas S. ; Marder, Stephen R. ; Medeiros, Helena ; Morley, Christopher P. ; Rapaport, Mark H. ; Knowles, James A. ; McCarroll, Steven A. ; Lowenstein, Daniel H. ; Goldstein, David B.

American journal of human genetics, 2019-08, Vol.105 (2), p.267-282 [Periódico revisado por pares]

United States: Elsevier Inc

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Mostrar Somente

  1. Recursos Online (14)
  2. Revistas revisadas por pares (14)

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.