Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lynn DeLisi"'
Autor:
Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas, Nicholas Bass, Tim B. Bigdeli, Gerome Breen, Evelyn J. Bromet, Peter F. Buckley, William E. Bunney, Jonas Bybjerg-Grauholm, William F. Byerley, Sinéad B. Chapman, Wei J. Chen, Claire Churchhouse, Nicholas Craddock, Caroline M. Cusick, Lynn DeLisi, Sheila Dodge, Michael A. Escamilla, Saana Eskelinen, Ayman H. Fanous, Stephen V. Faraone, Alessia Fiorentino, Laurent Francioli, Stacey B. Gabriel, Diane Gage, Sarah A. Gagliano Taliun, Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei-Hua Hall, Eija Hämäläinen, Henrike O. Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai-Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, Richard M. Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Dost Ongur, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark H. Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan Schatzberg, Edward Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine R. Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas H. Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden P. Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St. Clair, Ming T. Tsuang, Marquis P. Vawter, James T. Walters, Thomas M. Werge, Roel A. Ophoff, Patrick F. Sullivan, Michael J. Owen, Michael Boehnke, Michael C. O’Donovan, Benjamin M. Neale, Mark J. Daly
Publikováno v:
Singh, T, Poterba, T, Curtis, D, Akil, H, Al Eissa, M, Barchas, J D, Bass, N, Bigdeli, T B, Breen, G, Bromet, E J, Buckley, P F, Bunney, W E, Bybjerg-Grauholm, J, Byerley, W F, Chapman, S B, Chen, W J, Churchhouse, C, Craddock, N, Cusick, C M, DeLisi, L, Dodge, S, Escamilla, M A, Eskelinen, S, Fanous, A H, Faraone, S V, Fiorentino, A, Francioli, L, Gabriel, S B, Gage, D, Gagliano Taliun, S A, Ganna, A, Genovese, G, Glahn, D C, Grove, J, Hall, M H, Hämäläinen, E, Heyne, H O, Holi, M, Hougaard, D M, Howrigan, D P, Huang, H, Hwu, H G, Kahn, R S, Kang, H M, Karczewski, K J, Kirov, G, Knowles, J A, Lee, F S, Lehrer, D S, Lescai, F, Malaspina, D, Marder, S R, McCarroll, S A, McIntosh, A M, Medeiros, H, Milani, L, Morley, C P, Morris, D W, Mortensen, P B, Myers, R M, Nordentoft, M, O’Brien, N L, Olivares, A M, Ongur, D, Ouwehand, W H, Palmer, D S, Paunio, T, Quested, D, Rapaport, M H, Rees, E, Rollins, B, Satterstrom, F K, Schatzberg, A, Scolnick, E, Scott, L J, Sharp, S I, Sklar, P, Smoller, J W, Sobell, J L, Solomonson, M, Stahl, E A, Stevens, C R, Suvisaari, J, Tiao, G, Watson, S J, Watts, N A, Blackwood, D H, Børglum, A D, Cohen, B M, Corvin, A P, Esko, T, Freimer, N B, Glatt, S J, Hultman, C M, McQuillin, A, Palotie, A, Pato, C N, Pato, M T, Pulver, A E, St. Clair, D, Tsuang, M T, Vawter, M P, Walters, J T, Werge, T M, Ophoff, R A, Sullivan, P F, Owen, M J, Boehnke, M, O’Donovan, M C, Neale, B M & Daly, M J 2022, ' Rare coding variants in ten genes confer substantial risk for schizophrenia ', Nature, vol. 604, no. 7906, pp. 509-516 . https://doi.org/10.1038/s41586-022-04556-w
Singh, T, Poterba, T, Curtis, D, Akil, H, Al Eissa, M, Barchas, J D, Bass, N, Bigdeli, T B, Breen, G, Bromet, E J, Buckley, P F, Bunney, W E, Bybjerg-Grauholm, J, Byerley, W F, Chapman, S B, Chen, W J, Churchhouse, C, Craddock, N, Cusick, C M, DeLisi, L, Dodge, S, Escamilla, M A, Eskelinen, S, Fanous, A H, Faraone, S V, Fiorentino, A, Francioli, L, Gabriel, S B, Gage, D, Gagliano Taliun, S A, Ganna, A, Genovese, G, Glahn, D C, Grove, J, Hall, M-H, Hämäläinen, E, Heyne, H O, Holi, M, Hougaard, D M, Howrigan, D P, Huang, H, Hwu, H-G, Kahn, R S, Kang, H M, Karczewski, K J, Kirov, G, Knowles, J A, Lee, F S, Lehrer, D S, Lescai, F, Malaspina, D, Marder, S R, McCarroll, S A, McIntosh, A M, Medeiros, H, Milani, L, Morley, C P, Morris, D W, Mortensen, P B, Myers, R M, Nordentoft, M, O'Brien, N L, Olivares, A M, Ongur, D, Ouwehand, W H, Palmer, D S, Paunio, T, Quested, D, Rapaport, M H, Rees, E, Rollins, B, Satterstrom, F K, Schatzberg, A, Scolnick, E, Scott, L J, Sharp, S I, Sklar, P, Smoller, J W, Sobell, J L, Solomonson, M, Stahl, E A, Stevens, C R, Suvisaari, J, Tiao, G, Watson, S J, Watts, N A, Blackwood, D H, Børglum, A D, Cohen, B M, Corvin, A P, Esko, T, Freimer, N B, Glatt, S J, Hultman, C M, McQuillin, A, Palotie, A, Pato, C N, Pato, M T, Pulver, A E, St Clair, D, Tsuang, M T, Vawter, M P, Walters, J T, Werge, T M, Ophoff, R A, Sullivan, P F, Owen, M J, Boehnke, M, O'Donovan, M C, Neale, B M & Daly, M J 2022, ' Rare coding variants in ten genes confer substantial risk for schizophrenia ', Nature, vol. 604, no. 7906, pp. 509-516 . https://doi.org/10.1038/s41586-022-04556-w
Nature, 604(7906), 509-516. Nature Publishing Group
Nature
Singh, T, Poterba, T, Curtis, D, Akil, H, Al Eissa, M, Barchas, J D, Bass, N, Bigdeli, T B, Breen, G, Bromet, E J, Buckley, P F, Bunney, W E, Bybjerg-Grauholm, J, Byerley, W F, Chapman, S B, Chen, W J, Churchhouse, C, Craddock, N, Cusick, C M, DeLisi, L, Dodge, S, Escamilla, M A, Eskelinen, S, Fanous, A H, Faraone, S V, Fiorentino, A, Francioli, L, Gabriel, S B, Gage, D, Gagliano Taliun, S A, Ganna, A, Genovese, G, Glahn, D C, Grove, J, Hall, M-H, Hämäläinen, E, Heyne, H O, Holi, M, Hougaard, D M, Howrigan, D P, Huang, H, Hwu, H-G, Kahn, R S, Kang, H M, Karczewski, K J, Kirov, G, Knowles, J A, Lee, F S, Lehrer, D S, Lescai, F, Malaspina, D, Marder, S R, McCarroll, S A, McIntosh, A M, Medeiros, H, Milani, L, Morley, C P, Morris, D W, Mortensen, P B, Myers, R M, Nordentoft, M, O'Brien, N L, Olivares, A M, Ongur, D, Ouwehand, W H, Palmer, D S, Paunio, T, Quested, D, Rapaport, M H, Rees, E, Rollins, B, Satterstrom, F K, Schatzberg, A, Scolnick, E, Scott, L J, Sharp, S I, Sklar, P, Smoller, J W, Sobell, J L, Solomonson, M, Stahl, E A, Stevens, C R, Suvisaari, J, Tiao, G, Watson, S J, Watts, N A, Blackwood, D H, Børglum, A D, Cohen, B M, Corvin, A P, Esko, T, Freimer, N B, Glatt, S J, Hultman, C M, McQuillin, A, Palotie, A, Pato, C N, Pato, M T, Pulver, A E, St Clair, D, Tsuang, M T, Vawter, M P, Walters, J T, Werge, T M, Ophoff, R A, Sullivan, P F, Owen, M J, Boehnke, M, O'Donovan, M C, Neale, B M & Daly, M J 2022, ' Rare coding variants in ten genes confer substantial risk for schizophrenia ', Nature, vol. 604, no. 7906, pp. 509-516 . https://doi.org/10.1038/s41586-022-04556-w
Nature, 604(7906), 509-516. Nature Publishing Group
Nature
Rare coding variation has historically provided the most direct connections between gene function and disease pathogenesis. By meta-analysing the whole exomes of 24,248 schizophrenia cases and 97,322 controls, we implicate ultra-rare coding variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe2ccc8fbcc9e1444b626bc8351e653
https://pure.au.dk/portal/da/publications/rare-coding-variants-in-ten-genes-confer-substantial-risk-for-schizophrenia(18614934-0efa-4d5e-be5b-93b19a40453d).html
https://pure.au.dk/portal/da/publications/rare-coding-variants-in-ten-genes-confer-substantial-risk-for-schizophrenia(18614934-0efa-4d5e-be5b-93b19a40453d).html
Autor:
Michael Gill, Homero Vallada, David Collier, Pak Sham, Peter Holmans, Robin Murray, Peter McGuffin, Shin Nanko, Mike Owen, Stylianos Antonarakis, David Housman, Haig Kazazian, Gerald Nestadt, Ann E. Pulver, Richard E. Straub, Charles J. MacLean, Dermot Walsh, Kenneth S. Kendler, Lynn DeLisi, Mihael Polymeropoulos, Hilary Coon, William Byerley, Ray Lofthouse, Elliot Gershon, Lynn Golden, Timothy Crow, Robert Freedman, Claudine Laurent, Sylvie Bodeau-Pean, Thierry d'Amato, Maurice Jay, Dominique Campion, Jacques Mallet, Dieter B. Wildenauer, Bernard Lerer, Margot Albus, Manfred Ackenheil, Richard P. Ebstein, Joachim Hallmayer, Wolfgang Maier, Hugh Gurling, David Curtis, Gusharon Kalsi, Jon Brynjolfsson, Thordur Sigmundson, Hannes Petursson, Douglas Blackwood, Walter Muir, David St. Clair, Lin He, Susan Maguire, Hans W. Moises, Hai-Gwo Hwu, Liu Yang, Claudia Wiese, Li Tao, Xiehe Liu, Helgi Kristbjarnason, Douglas F. Levinson, Bryan J. Mowry, Helen Donis-Keller, Nicholas K. Hayward, Raymond R. Crowe, Jeremy M. Silverman, Derek J. Nancarrow, Christina M. Read
Publikováno v:
American Journal of Medical Genetics. 67:40-45
Several groups have reported weak evidence for linkage between schizophrenia and genetic markers located on chromosome 22q using the lod score method of analysis. However these findings involved different genetic markers and methods of analysis, and
Autor:
Lynn DeLisi, Alice Mule
Publikováno v:
Schizophrenia Research. 136:S1