Works by Klei, Lambertus

Results: 41

Discovering genetic ancestry using spectral graph theory.

Published in:

Genetic Epidemiology, 2010, v. 34, n. 1, p. 51, doi. 10.1002/gepi.20434

By:

Lee, Ann B.;
Luca, Diana;
Klei, Lambertus;
Devlin, Bernie;
Roeder, Kathryn

Publication type:

Article

Pleiotropy and principal components of heritability combine to increase power for association analysis.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 1, p. 9, doi. 10.1002/gepi.20257

By:

Klei, Lambertus;
Luca, Diana;
Devlin, B.;
Roeder, Kathryn

Publication type:

Article

Most genetic risk for autism resides with common variation.

Published in:

Nature Genetics, 2014, v. 46, n. 8, p. 881, doi. 10.1038/ng.3039

By:

Gaugler, Trent;
Klei, Lambertus;
Sanders, Stephan J;
Bodea, Corneliu A;
Goldberg, Arthur P;
Lee, Ann B;
Mahajan, Milind;
Manaa, Dina;
Pawitan, Yudi;
Reichert, Jennifer;
Ripke, Stephan;
Sandin, Sven;
Sklar, Pamela;
Svantesson, Oscar;
Reichenberg, Abraham;
Hultman, Christina M;
Devlin, Bernie;
Roeder, Kathryn;
Buxbaum, Joseph D

Publication type:

Article

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.

Published in:

Nature Genetics, 2012, v. 44, n. 12, p. 1349, doi. 10.1038/ng.2466

By:

Whitcomb, David C;
LaRusch, Jessica;
Krasinskas, Alyssa M;
Klei, Lambertus;
Smith, Jill P;
Brand, Randall E;
Neoptolemos, John P;
Lerch, Markus M;
Tector, Matt;
Sandhu, Bimaljit S;
Guda, Nalini M;
Orlichenko, Lidiya;
Albert, Marilyn S;
Albin, Roger L;
Apostolova, Liana G;
Arnold, Steven E;
Baldwin, Clinton T;
Barber, Robert;
Barnes, Lisa L;
Beach, Thomas G

Publication type:

Article

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.

Published in:

Nature Genetics, 2011, v. 43, n. 7, p. 699, doi. 10.1038/ng.859

By:

Höglinger, Günter U.;
Melhem, Nadine M.;
Dickson, Dennis W.;
Sleiman, Patrick M. A.;
Li-San Wang;
Klei, Lambertus;
Rademakers, Rosa;
de Silva, Rohan;
Litvan, Irene;
Riley, David E.;
van Swieten, John C.;
Heutink, Peter;
Wszolek, Zbigniew K.;
Uitti, Ryan J.;
Vandrovcova, Jana;
Hurtig, Howard I.;
Gross, Rachel G.;
Maetzler, Walter;
Goldwurm, Stefano;
Tolosa, Eduardo

Publication type:

Article

Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

Published in:

2009

By:

Silverberg, Mark S;
Cho, Judy H;
Rioux, John D;
McGovern, Dermot P B;
Wu, Jing;
Annese, Vito;
Achkar, Jean-Paul;
Goyette, Philippe;
Scott, Regan;
Xu, Wei;
Barmada, M Michael;
Klei, Lambertus;
Daly, Mark J;
Abraham, Clara;
Bayless, Theodore M;
Bossa, Fabrizio;
Griffiths, Anne M;
Ippoliti, Andrew F;
Lahaie, Raymond G;
Latiano, Anna

Publication type:

Correction Notice

Ulcerative colitis–risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

Published in:

Nature Genetics, 2009, v. 41, n. 2, p. 216, doi. 10.1038/ng.275

By:

Silverberg, Mark S.;
Cho, Judy H.;
Rioux, John D.;
McGovern, Dermot P. B.;
Jing Wu;
Annese, Vito;
Achkar, Jean-Paul;
Goyette, Philippe;
Scott, Regan;
Wei Xu;
Barmada, M. Michael;
Klei, Lambertus;
Daly, Mark J.;
Abraham, Clara;
Bayless, Theodore M.;
Bossa, Fabrizio;
Griffiths, Anne M.;
Ippoliti, Andrew F.;
Lahaie, Raymond G.;
Latiano, Anna

Publication type:

Article

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk.

Published in:

Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02071-0

By:

McKinney, Brandon C.;
McClain, Lora L.;
Hensler, Christopher M.;
Wei, Yue;
Klei, Lambertus;
Lewis, David A.;
Devlin, Bernie;
Wang, Jiebiao;
Ding, Ying;
Sweet, Robert A.

Publication type:

Article

Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart.

Published in:

Human Brain Mapping, 2020, v. 41, n. 15, p. 4187, doi. 10.1002/hbm.25118

By:

Jalbrzikowski, Maria;
Liu, Fuchen;
Foran, William;
Klei, Lambertus;
Calabro, Finnegan J.;
Roeder, Kathryn;
Devlin, Bernie;
Luna, Beatriz

Publication type:

Article

Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children.

Published in:

2012

By:

Brehm JM;
Acosta-Pérez E;
Klei L;
Roeder K;
Barmada M;
Boutaoui N;
Forno E;
Kelly R;
Paul K;
Sylvia J;
Litonjua AA;
Cabana M;
Alvarez M;
Colón-Semidey A;
Canino G;
Celedón JC;
Brehm, John M;
Acosta-Pérez, Edna;
Klei, Lambertus;
Roeder, Kathryn

Publication type:

journal article

Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican Children.

Published in:

American Journal of Respiratory & Critical Care Medicine, 2012, v. 186, n. 2, p. 140, doi. 10.1164/rccm.201203-0431oc

By:

Brehm, John M.;
Acosta-Pérez, Edna;
Klei, Lambertus;
Roeder, Kathryn;
Barmada, Michael;
Boutaoui, Nadia;
Forno, Erick;
Kelly, Roxanne;
Paul, Kathryn;
Sylvia, Jody;
Litonjua, Augusto A.;
Cabana, Michael;
Alvarez, María;
Colón-Semidey, Angel;
Canino, Glorisa;
Celedón, Juan C.

Publication type:

Article

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation.

Published in:

Human Genetics, 2007, v. 121, n. 6, p. 675, doi. 10.1007/s00439-007-0358-7

By:

Devlin, Bernie;
Klei, Lambertus;
Myles-Worsley, Marina;
Tiobech, Josepha;
Otto, Caleb;
Byerley, William;
Roeder, Kathryn

Publication type:

Article

Testing for association based on excess allele sharing in a sample of related cases and controls.

Published in:

Human Genetics, 2007, v. 121, n. 5, p. 549, doi. 10.1007/s00439-007-0345-z

By:

Klei, Lambertus;
Roeder, Kathyrn

Publication type:

Article

Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia.

Published in:

Human Genetics, 2005, v. 117, n. 4, p. 349, doi. 10.1007/s00439-005-1320-1

By:

Klei, Lambertus;
Bacanu, Silviu-Alin;
Myles-Worsley, Marina;
Galke, Brandi;
Weiting Xie;
Tiobech, Josepha;
Otto, Caleb;
Roeder, Kathyrn;
Devlin, Bernie;
Byerley, William

Publication type:

Article

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 6, p. 521, doi. 10.1002/ajmg.b.32255

By:

Melhem, Nadine M.;
Lu, Cong;
Dresbold, Cara;
Middleton, Frank A.;
Klei, Lambertus;
Wood, Shawn;
Faraone, Stephen V.;
Vinogradov, Sophia;
Tiobech, Josepha;
Yano, Victor;
Roeder, Kathryn;
Byerley, William;
Myles‐Worsley, Marina;
Devlin, Bernie

Publication type:

Article

GENETIC RISK FOR SCHIZOPHRENIA AND PSYCHOSIS IN ALZHEIMER DISEASE.

Published in:

Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P973, doi. 10.1016/j.jalz.2017.06.1313

By:

Ann A DeMichele-Sweet, Mary;
Weamer, Elise A.;
Lambertus, Klei;
Vrana, Dylan T.;
Hollingshead, Deborah J.;
Seltman, Howard J.;
Sims, Rebecca;
Foroud, Tatiana;
Hernandez, Isabel;
Moreno-Grau, Sonia;
Tarraga, Lluis;
Boada, Mercè;
Ruiz, Agustin;
Williams, Julie;
Mayeux, Richard;
lopez, Oscar L.;
Sibille, Etienne L.;
Kamboh, M. Ilyas;
Devlin, Bernie;
Sweet, Robert A.

Publication type:

Article

Genome-Wide Association Study for Alzheimer’s Disease with Psychotic Symptoms

Published in:

2011

By:

Hollingworth, Paul;
Sweet, Robert;
Sims, Rebecca;
Harold, Denise;
Abraham, Richard;
Gerrish, Amy;
Devlin, Bernie;
Klei, Lambertus;
Barmada, Michael;
Demirci, Yesim;
DeKosky, Steven;
Lopez, Oscar;
Peter Passmore;
Mayeux, Richard;
Kamboh, Ilyas;
Williams, Julie

Publication type:

Abstract

Heritability of Morningness‐Eveningness and Self‐Report Sleep Measures in a Family‐Based Sample of 521 Hutterites.

Published in:

Chronobiology International: The Journal of Biological & Medical Rhythm Research, 2005, v. 22, n. 6, p. 1041, doi. 10.1080/07420520500397959

By:

Klei, Lambertus;
Reitz, Patrick;
Miller, Mary;
Wood, Joel;
Maendel, Selma;
Gross, David;
Waldner, Tony;
Eaton, Joseph;
Monk, Timothy H.;
Nimgaonkar, Vishwajit L.

Publication type:

Article

Cohort profile: Epidemiology and Genetics of Obsessive-compulsive disorder and chronic tic disorders in Sweden (EGOS).

Published in:

2020

By:

Mahjani, Behrang;
Dellenvall, Karin;
Grahnat, Anna-Carin Säll;
Karlsson, Gun;
Tuuliainen, Aki;
Reichert, Jennifer;
Mahjani, Christina G.;
Klei, Lambertus;
De Rubeis, Silvia;
Reichenberg, Abraham;
Devlin, Bernie;
Hultman, Christina M.;
Buxbaum, Joseph D.;
Sandin, Sven;
Grice, Dorothy E.

Publication type:

journal article

Individual common variants exert weak effects on the risk for autism spectrum disorderspi.

Published in:

Human Molecular Genetics, 2012, v. 21, n. 21, p. 4781, doi. 10.1093/hmg/dds301

By:

Anney, Richard;
Klei, Lambertus;
Pinto, Dalila;
Almeida, Joana;
Bacchelli, Elena;
Baird, Gillian;
Bolshakova, Nadia;
Bölte, Sven;
Bolton, Patrick F.;
Bourgeron, Thomas;
Brennan, Sean;
Brian, Jessica;
Casey, Jillian;
Conroy, Judith;
Correia, Catarina;
Corsello, Christina;
Crawford, Emily L.;
de Jonge, Maretha;
Delorme, Richard;
Duketis, Eftichia

Publication type:

Article

A genome-wide scan for common alleles affecting risk for autism.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 20, p. 4072, doi. 10.1093/hmg/ddq307

By:

Anney, Richard;
Klei, Lambertus;
Pinto, Dalila;
Regan, Regina;
Conroy, Judith;
Magalhaes, Tiago R.;
Correia, Catarina;
Abrahams, Brett S.;
Sykes, Nuala;
Pagnamenta, Alistair T.;
Almeida, Joana;
Bacchelli, Elena;
Bailey, Anthony J.;
Baird, Gillian;
Battaglia, Agatino;
Berney, Tom;
Bolshakova, Nadia;
Bölte, Sven;
Bolton, Patrick F.;
Bourgeron, Thomas

Publication type:

Article

Candidate Gene Analysis of Femoral Neck Trabecular and Cortical Volumetric Bone Mineral Density in Older Men.

Published in:

Journal of Bone & Mineral Research, 2010, v. 25, n. 2, p. 330, doi. 10.1359/jbmr.090729

By:

Yerges, Laura M.;
Klei, Lambertus;
Cauley, Jane A.;
Roeder, Kathryn;
Kammerer, Candace M.;
Ensrud, Kristine E.;
Nestlerode, Cara S.;
Lewis, Cora;
Lang, Thomas F.;
Barrett-Connor, Elizabeth;
Moffett, Susan P.;
Hoffman, Andrew R.;
Ferrell, Robert E.;
Orwoll, Eric S.;
Zmuda, Joseph M.

Publication type:

Article

High-Density Association Study of 383 Candidate Genes for Volumetric BMD at the Femoral Neck and Lumbar Spine Among Older Men.

Published in:

Journal of Bone & Mineral Research, 2009, v. 24, n. 12, p. 2039, doi. 10.1359/JBMR.090524

By:

Yerges, Laura M.;
Klei, Lambertus;
Cauley, Jane A.;
Roeder, Kathryn;
Kammerer, Candace M.;
Moffett, Susan P.;
Ensrud, Kristine E.;
Nestlerode, Cara S.;
Marshall, Lynn M.;
Hoffman, Andrew R.;
Lewis, Cora;
Lang, Thomas F.;
Barrett-Connor, Elizabeth;
Ferrell, Robert E.;
Orwoll, Eric S.;
Zmuda, Joseph M.

Publication type:

Article

Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies.

Published in:

Statistics in Medicine, 2010, v. 29, n. 28, p. 2932, doi. 10.1002/sim.4057

By:

Crossett, Andrew;
Kent, Brian P.;
Klei, Lambertus;
Ringquist, Steven;
Trucco, Massimo;
Roeder, Kathryn;
Devlin, Bernie

Publication type:

Article

How rare and common risk variation jointly affect liability for autism spectrum disorder.

Published in:

Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00466-2

By:

Klei, Lambertus;
McClain, Lora Lee;
Mahjani, Behrang;
Panayidou, Klea;
De Rubeis, Silvia;
Grahnat, Anna-Carin Säll;
Karlsson, Gun;
Lu, Yangyi;
Melhem, Nadine;
Xu, Xinyi;
Reichenberg, Abraham;
Sandin, Sven;
Hultman, Christina M.;
Buxbaum, Joseph D.;
Roeder, Kathryn;
Devlin, Bernie

Publication type:

Article

Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder.

Published in:

Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00465-3

By:

Mahjani, Behrang;
De Rubeis, Silvia;
Gustavsson Mahjani, Christina;
Mulhern, Maureen;
Xu, Xinyi;
Klei, Lambertus;
Satterstrom, F. Kyle;
Fu, Jack;
Talkowski, Michael E.;
Reichenberg, Abraham;
Sandin, Sven;
Hultman, Christina M.;
Grice, Dorothy E.;
Roeder, Kathryn;
Devlin, Bernie;
Buxbaum, Joseph D.

Publication type:

Article

Heritable Composite Phenotypes Defined by Combinations of Conduct Problem, Depression, and Temperament Features: Contributions to risk for Alcohol Problems.

Published in:

Research on Child & Adolescent Psychopathology, 2024, v. 52, n. 4, p. 535, doi. 10.1007/s10802-023-01129-x

By:

Wang, Frances L.;
Klei, Lambertus;
Devlin, Bernie;
Molina, Brooke S.G.;
Chassin, Laurie

Publication type:

Article

The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.

Published in:

Nature Communications, 2015, v. 6, n. 3, p. 6404, doi. 10.1038/ncomms7404

By:

Cotney, Justin;
Muhle, Rebecca A.;
Sanders, Stephan J.;
Liu, Li;
Willsey, A. Jeremy;
Niu, Wei;
Liu, Wenzhong;
Klei, Lambertus;
Lei, Jing;
Yin, Jun;
Reilly, Steven K.;
Tebbenkamp, Andrew T.;
Bichsel, Candace;
Pletikos, Mihovil;
Sestan, Nenad;
Roeder, Kathryn;
State, Matthew W.;
Devlin, Bernie;
Noonan, James P.

Publication type:

Article

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q11.2, Specifically Breakpoints 1 to 2.

Published in:

Autism Research: Official Journal of the International Society for Autism Research, 2014, v. 7, n. 3, p. 355, doi. 10.1002/aur.1378

By:

Chaste, Pauline;
Sanders, Stephan J.;
Mohan, Kommu N.;
Klei, Lambertus;
Song, Youeun;
Murtha, Michael T.;
Hus, Vanessa;
Lowe, Jennifer K.;
Willsey, A. Jeremy;
Moreno‐De‐Luca, Daniel;
Yu, Timothy W.;
Fombonne, Eric;
Geschwind, Daniel;
Grice, Dorothy E.;
Ledbetter, David H.;
Lord, Catherine;
Mane, Shrikant M.;
Martin, Donna M.;
Morrow, Eric M.;
Walsh, Christopher A.

Publication type:

Article

MULTIPLE GENOMIC MEASURES OF SCHIZOPHRENIA RISK ARE RELATED TO CORTICAL THICKNESS IN TYPICALLY DEVELOPING YOUTH AND YOUNG ADULTS.

Published in:

Schizophrenia Bulletin, 2020, v. 46, p. S27, doi. 10.1093/schbul/sbaa028.061

By:

Jalbrzikowski, Maria;
Klei, Lambertus;
Foran, William;
Luna, Beatriz;
Devlin, Bernie

Publication type:

Article

T20. POLYGENIC RISK FOR SCHIZOPHRENIA IS ASSOCIATED WITH HIPPOCAMPAL VOLUME IN TYPICALLY DEVELOPING YOUTH.

Published in:

Schizophrenia Bulletin, 2019, v. 45, p. S211, doi. 10.1093/schbul/sbz019.300

By:

Jalbrzikowski, Maria;
Klei, Lambertus;
Devlin, Bernie

Publication type:

Article

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects.

Published in:

2013

By:

Wiener, Howard;
Klei, Lambertus;
Calkins, Monica;
Wood, Joel;
Nimgaonkar, Vishwajit;
Gur, Ruben;
Bradford, L. DiAnne;
Richard, Jan;
Edwards, Neil;
Savage, Robert;
Kwentus, Joseph;
Allen, Trina;
McEvoy, Joseph;
Santos, Alberto;
Gur, Raquel;
Devlin, Bernie;
Go, Rodney

Publication type:

Journal Article

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects.

Published in:

Schizophrenia Bulletin, 2013, v. 39, n. 2, p. 464, doi. 10.1093/schbul/sbr161

By:

Wiener, Howard;
Klei, Lambertus;
Calkins, Monica;
Wood, Joel;
Nimgaonkar, Vishwajit;
Gur, Ruben;
Bradford, L. DiAnne;
Richard, Jan;
Edwards, Neil;
Savage, Robert;
Kwentus, Joseph;
Allen, Trina;
McEvoy, Joseph;
Santos, Alberto;
Gur, Raquel;
Devlin, Bernie;
Go, Rodney

Publication type:

Article

Evaluation of HLA Polymorphisms in Relation to Schizophrenia Risk and Infectious Exposure.

Published in:

2012

By:

Bamne, Mikhil;
Wood, Joel;
Chowdari, Kodavali;
Watson, Annie M;
Celik, Cemil;
Mansour, Hader;
Klei, Lambertus;
Gur, Ruben C;
Bradford, L Dianne;
Calkins, Monica E;
Santos, Alberto B;
Edwards, Neil;
Kwentus, Joseph;
McEvoy, Joseph P;
Allen, Trina B;
Savage, Robert M;
Nasrallah, Henry A;
Gur, Raquel E;
Perry, Rodney T;
Go, Rodney C P

Publication type:

Journal Article

Evaluation of HLA Polymorphisms in Relation to Schizophrenia Risk and Infectious Exposure.

Published in:

Schizophrenia Bulletin, 2012, v. 38, n. 6, p. 1149, doi. 10.1093/schbul/sbs087

By:

Bamne, Mikhil;
Wood, Joel;
Chowdari, Kodavali;
Watson, Annie M.;
Celik, Cemil;
Mansour, Hader;
Klei, Lambertus;
Gur, Ruben C.;
Bradford, L. DiAnne;
Calkins, Monica E.;
Santos, Alberto B.;
Edwards, Neil;
Kwentus, Joseph;
McEvoy, Joseph P.;
Allen, Trina B.;
Savage, Robert M.;
Nasrallah, Henry A.;
Gur, Raquel E.;
Perry, Rodney T.;
Go, Rodney C.P.

Publication type:

Article

Genetic associations with psychosis and affective disturbance in Alzheimer's disease.

Published in:

Alzheimer's & Dementia: Translational Research & Clinical Interventions, 2024, v. 10, n. 2, p. 1, doi. 10.1002/trc2.12472

By:

Antonsdottir, Inga Margret;
Creese, Byron;
Klei, Lambertus;
DeMichele‐Sweet, Mary Ann A.;
Weamer, Elise A.;
Garcia‐Gonzalez, Pablo;
Marquie, Marta;
Boada, Mercè;
Alarcón‐Martín, Emilio;
Valero, Sergi;
Liu, Yushi;
Hooli, Basavaraj;
Aarsland, Dag;
Selbaek, Geir;
Bergh, Sverre;
Rongve, Arvid;
Saltvedt, Ingvild;
Skjellegrind, Håvard K.;
Engdahl, Bo;
Andreassen, Ole A.

Publication type:

Article

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder.

Published in:

Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01290-1

By:

Piantadosi, Sean C.;
McClain, Lora L.;
Klei, Lambertus;
Wang, Jiebiao;
Chamberlain, Brittany L.;
Springer, Sara A.;
Lewis, David A.;
Devlin, Bernie;
Ahmari, Susanne E.

Publication type:

Article

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.

Published in:

Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-22

By:

Li Liu;
Jing Lei;
Sanders, Stephan J.;
Willsey, Arthur Jeremy;
Yan Kou;
Cicek, Abdullah Ercument;
Klei, Lambertus;
Cong Lu;
Xin He;
Mingfeng Li;
Muhle, Rebecca A.;
Ma'ayan, Avi;
Noonan, James P.;
Sestan, Nenad;
McFadden, Kathryn A.;
State, Matthew W.;
Buxbaum, Joseph D.;
Devlin, Bernie;
Roeder, Kathryn

Publication type:

Article

Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.

Published in:

Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-31

By:

Gupta, Abha R.;
Pirruccello, Michelle;
Feng Cheng;
Hyo Jung Kang;
Fernandez, Thomas V.;
Baskin, Jeremy M.;
Murim Choi;
Li Liu;
Ercan-Sencicek, Adife Gulhan;
Murdoch, John D.;
Klei, Lambertus;
Neale, Benjamin M.;
Franjic, Daniel;
Daly, Mark J.;
Lifton, Richard P.;
De Camilli, Pietro;
Hongyu Zhao;
Šestan, Nenad;
State, Matthew W.

Publication type:

Article

Common genetic variants, acting additively, are a major source of risk for autism.

Published in:

Molecular Autism, 2012, v. 3, n. 1, p. 1, doi. 10.1186/2040-2392-3-9

By:

Klei, Lambertus;
Sanders, Stephan J.;
Murtha, Michael T.;
Hus, Vanessa;
Lowe, Jennifer K.;
Jeremy Willsey, A.;
Moreno-De-Luca, Daniel;
Yu, Timothy W.;
Fombonne, Eric;
Geschwind, Daniel;
Grice, Dorothy E.;
Ledbetter, David H.;
Lord, Catherine;
Mane, Shrikant M.;
Martin, Christa Lese;
Martin, Donna M.;
Morrow, Eric M.;
Walsh, Christopher A.;
Melhem, Nadine M.;
Chaste, Pauline

Publication type:

Article

Functional impact of global rare copy number variation in autism spectrum disorders.

Published in:

Nature, 2010, v. 466, n. 7304, p. 368, doi. 10.1038/nature09146

By:

Pinto, Dalila;
Pagnamenta, Alistair T.;
Klei, Lambertus;
Anney, Richard;
Merico, Daniele;
Regan, Regina;
Conroy, Judith;
Magalhaes, Tiago R.;
Correia, Catarina;
Abrahams, Brett S.;
Almeida, Joana;
Bacchelli, Elena;
Bader, Gary D.;
Bailey, Anthony J.;
Baird, Gillian;
Battaglia, Agatino;
Berney, Tom;
Bolshakova, Nadia;
Bölte, Sven;
Bolton, Patrick F.

Publication type:

Article