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James A. Knowles

Rutgers University

68H指数
172论文数
2.6W被引数
收录论文 53
发表时间
Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia基于全基因组序列的关联分析:非裔美国人个体中双相障碍与精神分裂症的研究
err2025-08-30
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errRunjia Li; Sarah A. Gagliano Taliun; Kevin Liao; Matthew Flickinger; Janet L. Sobell; Giulio Genovese; Adam E. Locke; Rebeca Rothwell Chiu; Jonathon LeFaive; Jiongming Wang; Taylor Martins; Sinéad Chapman; Anna Neumann; Robert E. Handsaker; Donna K. Arnett; Kathleen C. Barnes; Eric Boerwinkle; David Braff; Brian E. Cade; Myriam Fornage; Richard A. Gibbs; Karin F. Hoth; Lifang Hou; Charles Kooperberg; Ruth J.F. Loos; Ginger A. Metcalf; Courtney G. Montgomery; Alanna C. Morrison; Zhaohui S. Qin; Susan Redline; Alexander P. Reiner; Stephen S. Rich; Jerome I. Rotter; Kent D. Taylor; Karine A. Viaud-Martinez; Tim B. Bigdeli; Stacey Gabriel; Sebastian Zollner; Albert V. Smith; Goncalo Abecasis; Steve A. McCarroll; Michele T. Pato; Carlos N. Pato; Michael Boehnke; James Knowles; Hyun Min Kang; Roel A. Ophoff; Jason Ernst; Laura J. Scott
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Prevalence and correlates of lifetime suicide attempt in obsessive-compulsive disorder with major depression
err2023-05-01
err1
errOAAI
errSamuels, Jack; Bienvenu, Joseph; Krasnow, Janice; Grados, Marco A.; Cullen, Bernadette A.; Goes, Fernando S.; McLaughlin, Nicole C.; Rasmussen, Steven A.; Fyer, Abby J.; Knowles, James A.; McCracken, James T.; Geller, Dan; Riddle, Mark A.; Piacentini, John; Stewart, S. Evelyn; Greenberg, Benjamin D.; Nestadt, Gerald; Nestadt, Paul
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Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations罕见的蛋白质截断变体赋予的精神分裂症风险在不同人群中是保守的
err2023-03-13
err21
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errLiu, Dongjing; Meyer, Dara; Fennessy, Brian; Feng, Claudia; Cheng, Esther; Johnson, Jessica; Park, You Jeong; Rieder, Marysia-Kolbe; Ascolillo, Steven; de Pins, Agathe; Dobbyn, Amanda; Lebovitch, Dannielle; Moya, Emily; Nguyen, Tan-Hoang; Wilkins, Lillian; Hassan, Arsalan; Aghanwa, Henry; Burdick, Katherine E.; Buxbaum, Joseph D.; Domenici, Enrico; Frangou, Sophia; Hartmann, Annette M.; Laurent-Levinson, Claudine; Malhotra, Dheeraj; Pato, Carlos N.; Pato, Michele T.; Ressler, Kerry; Roussos, Panos; Rujescu, Dan; Arango, Celso; Bertolino, Alessandro; Blasi, Giuseppe; Bocchio-Chiavetto, Luisella; Campion, Dominique; Carr, Vaughan; Fullerton, Janice M.; Gennarelli, Massimo; Gonzalez-Penas, Javier; Levinson, Douglas F.; Mowry, Bryan; Nimgaokar, Vishwajit L.; Pergola, Giulio; Rampino, Antonio; Cervilla, Jorge A.; Rivera, Margarita; Schwab, Sibylle G.; Wildenauer, Dieter B.; Daly, Mark; Neale, Benjamin; Singh, Tarjinder; O'Donovan, Michael C.; Owen, Michael J.; Walters, James T.; Ayub, Muhammad; Malhotra, Anil K.; Lencz, Todd; Sullivan, Patrick F.; Sklar, Pamela; Stahl, Eli A.; Huckins, Laura M.; Charney, Alexander W.; Aghanwa, Henry S.; Ansari, Moin; Asif, Aftab; Aslam, Rubina; Ayuso, Jose L.; Bigdeli, Tim; Bignotti, Stefano; Bobes, Julio; Bradley, Bekh; Buckley, Peter; Cairns, Murray J.; Catts, Stanley V.; Chaudhry, Abdul Rashid; Cohen, David; Collins, Brett L.; Consoli, Angele; Costas, Javier; Crespo-Facorro, Benedicto; Daskalakis, Nikolaos P.; Davidson, Michael; Davis, Kenneth L.; Dickerson, Faith; Dogar, Imtiaz A.; Drapeau, Elodie; Fananas, Lourdes; Fanous, Ayman; Fatima, Warda; Fatjo, Mar; Filippich, Cheryl; Friedman, Joseph; Fullard, John F.; Georgakopoulos, Penelope; Giannitelli, Marianna; Giegling, Ina; Green, Melissa J.; Guillin, Olivier; Gutierrez, Blanca; Handoko, Herlina Y.; Hansen, Stella Kim; Haroon, Maryam; Haroutunian, Vahram; Henskens, Frans A.; Hussain, Fahad; Jablensky, Assen V.; Junejo, Jamil; Kelly, Brian J.; Khan, Shams-Ud-Din A.; Khan, Muhammad N. S.; Khan, Anisuzzaman; Khawaja, Hamid R.; Khizar, Bakht; Kleopoulos, Steven P.; Knowles, James; Konte, Bettina; Kusumawardhani, Agung A. A. A.; Leghari, Naeemullah; Liu, Xudong; Lori, Adriana; Loughland, Carmel M.; Mahmood, Khalid; Mahmood, Saqib; Malaspina, Dolores; Malik, Danish; McNaughton, Amy; Michie, Patricia T.; Michopolous, Vasiliki; Molina, Esther; Molto, Maria D.; Munir, Asim; Muntane, Gerard; Naeem, Farooq; Nancarrow, Derek J.; Nasar, Amina; Nasr, Tanvir; Ohaeri, Jude U.; Ott, Jurg; Pantelis, Christos; Periyasamy, Sathish; Pinto, Ana G.; Powers, Abigail; Ramos, Belen; Rana, Nusrat H.; Rapaport, Mark; Reichenberg, Abraham; Saker-Delye, Safaa; Schall, Ulrich; Schofield, Peter R.; Scott, Rodney J.; Shanahan, Megan; Weickert, Cynthia Shannon; Sjaarda, Calvin; Smith, Heather J.; Suarez-Rama, Jose Javier; Tariq, Muhammad; Thibaut, Florence; Tooney, Paul A.; Umar, Muhammad; Vilella, Elisabet; Weiser, Mark; Wu, Jin Qin; Yolken, Robert
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Characterisation of age and polarity at onset in bipolar disorder双相情感障碍发病时的年龄和极性特征
err2021-08-25
err18
errOAAI
errKalman, Janos L.; Loohuis, Loes M. Olde; Vreeker, Annabel; McQuillin, Andrew; Stahl, Eli A.; Ruderfer, Douglas; Grigoroiu-Serbanescu, Maria; Panagiotaropoulou, Georgia; Ripke, Stephan; Bigdeli, Tim B.; Stein, Frederike; Meller, Tina; Meinert, Susanne; Pelin, Helena; Streit, Fabian; Papiol, Sergi; Adams, Mark J.; Adolfsson, Rolf; Adorjan, Kristina; Agartz, Ingrid; Aminoff, Sofie R.; Anderson-Schmidt, Heike; Andreassen, Ole A.; Ardau, Raffaella; Aubry, Jean-Michel; Balaban, Ceylan; Bass, Nicholas; Baune, Bernhard T.; Bellivier, Frank; Benabarre, Antoni; Bengesser, Susanne; Berrettini, Wade H.; Boks, Marco P.; Bromet, Evelyn J.; Brosch, Katharina; Budde, Monika; Byerley, William; Cervantes, Pablo; Chillotti, Catina; Cichon, Sven; Clark, Scott R.; Comes, Ashley L.; Corvin, Aiden; Coryell, William; Craddock, Nick; Craig, David W.; Croarkin, Paul E.; Cruceanu, Cristiana; Czerski, Piotr M.; Dalkner, Nina; Dannlowski, Udo; Degenhardt, Franziska; Del Zompo, Maria; DePaulo, J. Raymond; Djurovic, Srdjan; Edenberg, Howard J.; Al Eissa, Mariam; Elvsashagen, Torbjorn; Etain, Bruno; Fanous, Ayman H.; Fellendorf, Frederike; Fiorentino, Alessia; Forstner, Andreas J.; Frye, Mark A.; Fullerton, Janice M.; Gade, Katrin; Garnham, Julie; Gershon, Elliot; Gill, Michael; Goes, Fernando S.; Gordon-Smith, Katherine; Grof, Paul; Guzman-Parra, Jose; Hahn, Tim; Hasler, Roland; Heilbronner, Maria; Heilbronner, Urs; Jamain, Stephane; Jimenez, Esther; Jones, Ian; Jones, Lisa; Jonsson, Lina; Kahn, Rene S.; Kelsoe, John R.; Kennedy, James L.; Kircher, Tilo; Kirov, George; Kittel-Schneider, Sarah; Klohn-Saghatolislam, Farah; Knowles, James A.; Kranz, Thorsten M.; Lagerberg, Trine Vik; Landen, Mikael; Lawson, William B.; Leboyer, Marion; Li, Qingqin S.; Maj, Mario; Malaspina, Dolores; Manchia, Mirko; Mayoral, Fermin; McElroy, Susan L.; McInnis, Melvin G.; McIntosh, Andrew M.; Medeiros, Helena; Melle, Ingrid; Milanova, Vihra; Mitchell, Philip B.; Monteleone, Palmiero; Monteleone, Alessio Maria; Nothen, Markus M.; Novak, Tomas; Nurnberger, John, I; O'Brien, Niamh; O'Connell, Kevin S.; O'Donovan, Claire; O'Donovan, Michael C.; Opel, Nils; Ortiz, Abigail; Owen, Michael J.; Palsson, Erik; Pato, Carlos; Pato, Michele T.; Pawlak, Joanna; Pfarr, Julia-Katharina; Pisanu, Claudia; Potash, James B.; Rapaport, Mark H.; Reich-Erkelenz, Daniela; Reif, Andreas; Reininghaus, Eva; Repple, Jonathan; Richard-Lepouriel, Helene; Rietschel, Marcella; Ringwald, Kai; Roberts, Gloria; Rouleau, Guy; Schaupp, Sabrina; Scheftner, William A.; Schmitt, Simon; Schofield, Peter R.; Schubert, K. Oliver; Schulte, Eva C.; Schweizer, Barbara; Senner, Fanny; Severino, Giovanni; Sharp, Sally; Slaney, Claire; Smeland, Olav B.; Sobell, Janet L.; Squassina, Alessio; Stopkova, Pavla; Strauss, John; Tortorella, Alfonso; Turecki, Gustavo; Twarowska-Hauser, Joanna; Veldic, Marin; Vieta, Eduard; Vincent, John B.; Xu, Wei; Zai, Clement C.; Zandi, Peter P.; Di Florio, Arianna; Smoller, Jordan W.; Biernacka, Joanna M.; McMahon, Francis J.; Alda, Martin; Muller-Myhsok, Bertram; Koutsouleris, Nikolaos; Falkai, Peter; Freimer, Nelson B.; Andlauer, Till F. M.; Schulze, Thomas G.; Ophoff, Roel A.
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Recurrent Rare Copy Number Variants Increase Risk for Esotropia复发性罕见拷贝数变异增加内斜视的风险
err2020-08-11
err9
errOAAI
errWhitman, Mary C.; Di Gioia, Silvio Alessandro; Chan, Wai-Man; Gelber, Alon; Pratt, Brandon M.; Bell, Jessica L.; Collins, Thomas E.; Knowles, James A.; Armoskus, Christopher; Pato, Michele; Pato, Carlos; Shaaban, Sherin; Staffieri, Sandra; MacKinnon, Sarah; Maconachie, Gail D. E.; Elder, James E.; Traboulsi, Elias I.; Gottlob, Irene; Mackey, David A.; Hunter, David G.; Engle, Elizabeth C.
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Deconvolution of transcriptional networks identifies TCF4 as a master regulator in schizophrenia
err2019-09-06
err41
errOAAI
errTorshizi, Abolfazl Doostparast; Armoskus, Chris; Zhang, Hanwen; Forrest, Marc P.; Zhang, Siwei; Souaiaia, Tade; Evgrafov, Oleg V.; Knowles, James A.; Duan, Jubao; Wang, Kai
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Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases罕见的拷贝数变异对双相情感障碍风险的贡献仅限于分裂情感病例
err2019-07-01
err43
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errCharney, Alexander W.; Stahl, Eli A.; Green, Elaine K.; Chen, Chia-Yen; Moran, Jennifer L.; Chambert, Kimberly; Belliveau, Richard A., Jr.; Forty, Liz; Gordon-Smith, Katherine; Lee, Phil H.; Bromet, Evelyn J.; Buckley, Peter F.; Escamilla, Michael A.; Fanous, Ayman H.; Fochtmann, Laura J.; Lehrer, Douglas S.; Malaspina, Dolores; Marder, Stephen R.; Morley, Christopher P.; Nicolini, Humberto; Perkins, Diana O.; Rakofsky, Jeffrey J.; Rapaport, Mark H.; Medeiros, Helena; Sobell, Janet L.; Backlund, Lena; Bergen, Sarah E.; Jureus, Anders; Schalling, Martin; Lichtenstein, Paul; Knowles, James A.; Burdick, Katherine E.; Jones, Ian; Jones, Lisa A.; Hultman, Christina M.; Perlis, Roy; Purcell, Shaun M.; McCarroll, Steven A.; Pato, Carlos N.; Pato, Michele T.; Di Florio, Ariana; Craddock, Nick; Landen, Mikael; Smoller, Jordan W.; Ruderfer, Douglas M.; Sklar, Pamela
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Genome-wide Burden of Rare Short Deletions Is Enriched in Major Depressive Disorder in Four Cohorts罕见短缺失的全基因组负担在四个队列的重性抑郁症中富集
err2019-06-01
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errZhang, Xianglong; Abdellaoui, Abdel; Rucker, James; de Jong, Simone; Potash, James B.; Weissman, Myrna M.; Shi, Jianxin; Knowles, James A.; Pato, Carlos; Pato, Michele; Sobell, Janet; Smit, Johannes H.; Hottenga, Jouke-Jan; de Geus, Eco J. C.; Lewis, Cathryn M.; Buttenschon, Henriette N.; Craddock, Nick; Jones, Ian; Jones, Lisa; McGuffin, Peter; Mors, Ole; Owen, Michael J.; Preisig, Martin; Rietschel, Marcella; Rice, John P.; Rivera, Margarita; Uher, Rudolf; Gejman, Pablo V.; Sanders, Alan R.; Boomsma, Dorret; Penninx, Brenda W. J. H.; Breen, Gerome; Levinson, Douglas F.
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POLYGENIC ADAPTATION UNDERLIES EVOLUTION OF BRAIN STRUCTURES AND BEHAVIORAL TRAITS
err2019-01-01
err1
PREAI
errDavis, Lea; Beiter, Evan; Khramtsova, Ekaterina; Van der Merwe, Celia; Chimusa, Emile; Simonti, Corinne; Stein, Dan; Capra, John; Knowles, James; Straub, Peter; Hucks, Donald; Stranger, Barbara
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CONTRIBUTIONS OF COMMON GENETIC VARIANTS TO SCHIZOPHRENIA RISK IN INDIVIDUALS WITH AFRICAN AND LATINO ANCESTRY
err2019-01-01
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PREAI
errBigdeli, Tim; Genovese, Giulio; Medeiros, Helena; Sobell, Janet; Knowles, James; Pato, Michele; Fanous, Ayman; McCarroll, Steven; Pato, Carlos
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Using 3D epigenomic maps of primary olfactory neuronal cells from living individuals to understand gene regulation
err2018-12-07
err42
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errRhie, Suhn K.; Schreiner, Shannon; Witt, Heather; Armoskus, Chris; Lay, Fides D.; Camarena, Adrian; Spitsyna, Valeria N.; Guo, Yu; Berman, Benjamin P.; Evgrafov, Oleg V.; Knowles, James A.; Farnham, Peggy J.
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Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder
err2018-08-07
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errYilmaz, Zeynep; Halvorsen, Matthew; Bryois, Julien; Yu, Dongmei; Thornton, Laura M.; Zerwas, Stephanie; Micali, Nadia; Moessner, Rainald; Burton, Christie L.; Zai, Gwyneth; Erdman, Lauren; Kas, Martien J.; Arnold, Paul D.; Davis, Lea K.; Knowles, James A.; Breen, Gerome; Scharf, Jeremiah M.; Nestadt, Gerald; Mathews, Carol A.; Bulik, Cynthia M.; Mattheisen, Manuel; Crowley, James J.
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Characterizing Neurotrophic Systems in the Primate Amygdala That are Relevant to Mediating and Treating Anxiety Disorders
err2018-05-01
err0
PREAI
errRoseboom, Patrick; Kovner, Rothem; Souaiaia, Tade; Lu, Jianfeng; Dong, Yi; Fathi, Ali; Tao, Yezheng; French, Delores; Fox, Andrew; Oler, Jonathan; Bhattacharyya, Anita; Zhang, Su-chun; Knowles, James; Kalin, Ned
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Integrating evolutionary and regulatory information with multispecies approach implicates genes and pathways in obsessive-compulsive disorder
err2017-10-17
err50
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errNoh, Hyun Ji; Tang, Ruqi; Flannick, Jason; O'Dushlaine, Colm; Swofford, Ross; Howrigan, Daniel; Genereux, Diane P.; Johnson, Jeremy; van Grootheest, Gerard; Grunblatt, Edna; Andersson, Erik; Djurfeldt, Diana R.; Patel, Paresh D.; Koltookian, Michele; Hultman, Christina M.; Pato, Michele T.; Pato, Carlos N.; Rasmussen, Steven A.; Jenike, Michael A.; Hanna, Gregory L.; Stewart, S. Evelyn; Knowles, James A.; Ruhrmann, Stephan; Grabe, Hans-Joergen; Wagner, Michael; Ruck, Christian; Mathews, Carol A.; Walitza, Susanne; Cath, Danielle C.; Feng, Guoping; Karlsson, Elinor K.; Lindblad-Toh, Kerstin
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Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD多基因风险评分和遗传力估计揭示了ASD和OCD之间的遗传关系
err2017-07-01
err41
PREAI
errGuo, W.; Samuels, J. F.; Wang, Y.; Cao, H.; Ritter, M.; Nestadt, P. S.; Krasnow, J.; Greenberg, B. D.; Fyer, A. J.; McCracken, J. T.; Geller, D. A.; Murphy, D. L.; Knowles, J. A.; Grados, M. A.; Riddle, M. A.; Rasmussen, S. A.; McLaughlin, N. C.; Nurmi, E. L.; Askland, K. D.; Culten, B. A.; Piacentini, J.; Pauls, D. L.; Bienvenu, O. J.; Stewart, S. E.; Goes, F. S.; Maher, B.; Pulver, A. E.; Valle, D.; Mattheisen, M.; Qian, J.; Nestad, G.; Shugart, Y. Y.
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
errNEURON
IF15
err2017-06-01
err133
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errHuang, Alden Y.; Yu, Dongmei; Davis, Lea K.; Sul, Jae Hoon; Tsetsos, Fotis; Ramensky, Vasily; Zelaya, Ivette; Ramos, Eliana Marisa; Osiecki, Lisa; Chen, Jason A.; McGrath, Lauren M.; Illmann, Cornelia; Sandor, Paul; Barr, Cathy L.; Grados, Marco; Singer, Harvey S.; Noethen, Markus M.; Hebebrand, Johannes; King, Robert A.; Dion, Yves; Rouleau, Guy; Budman, Cathy L.; Depienne, Christel; Worbe, Yulia; Hartmann, Andreas; Mueller-Vahl, Kirsten R.; Stuhrmann, Manfred; Aschauer, Harald; Stamenkovic, Mara; Schloegelhofer, Monika; Konstantinidis, Anastasios; Lyon, Gholson J.; McMahon, William M.; Barta, Csaba; Tarnok, Zsanett; Nagy, Peter; Batterson, James R.; Rizzo, Renata; Cath, Danielle C.; Wolanczyk, Tomasz; Berlin, Cheston; Malaty, Irene A.; Okun, Michael S.; Woods, Douglas W.; Rees, Elliott; Pato, Carlos N.; Pato, Michele T.; Knowles, James A.; Posthuma, Danielle; Pauls, David L.; Cox, Nancy J.; Neale, Benjamin M.; Freimer, Nelson B.; Paschou, Peristera; Mathews, Carol A.; Scharf, Jeremiah M.; Coppola, Giovanni
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Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder
err2017-01-10
err145
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errCharney, A. W.; Ruderfer, D. M.; Stahl, E. A.; Moran, J. L.; Chambert, K.; Belliveau, R. A.; Forty, L.; Gordon-Smith, K.; Di Florio, A.; Lee, P. H.; Bromet, E. J.; Buckley, P. F.; Escamilla, M. A.; Fanous, A. H.; Fochtmann, L. J.; Lehrer, D. S.; Malaspina, D.; Marder, S. R.; Morley, C. P.; Nicolini, H.; Perkins, D. O.; Rakofsky, J. J.; Rapaport, M. H.; Medeiros, H.; Sobell, J. L.; Green, E. K.; Backlund, L.; Bergen, S. E.; Jureus, A.; Schalling, M.; Lichtenstein, P.; Roussos, P.; Knowles, J. A.; Jones, I.; Jones, L. A.; Hultman, C. M.; Perlis, R. H.; Purcell, S. M.; McCarroll, S. A.; Pato, C. N.; Pato, M. T.; Craddock, N.; Landen, M.; Smoller, J. W.; Sklar, P.
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Reconstructing genetic history of Siberian and Northeastern European populations
err2016-12-13
err49
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errWong, Emily N. M.; Khrunin, Andrey; Nichols, Larissa; Pushkarev, Dmitry; Khokhrin, Denis; Verbenko, Dmitry; Evgrafov, Oleg; Knowles, James; Novembre, John; Limborska, Svetlana; Valouev, Anton
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