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Principles of haplotype mapping and potential applications to attention-deficit/hyperactivity disorderSKLAR, Pamela.Biological psychiatry (1969). 2005, Vol 57, Num 11, pp 1357-1366, issn 0006-3223, 10 p.Conference Paper

Genetics of bipolar disorderCRADDOCK, Nick; SKLAR, Pamela.Lancet (British edition). 2013, Vol 381, Num 9878, pp 1654-1662, issn 0140-6736, 9 p.Article

Genetics of bipolar disorder : successful start to a long journeyCRADDOCK, Nick; SKLAR, Pamela.Trends in genetics (Regular ed.). 2009, Vol 25, Num 2, pp 99-105, issn 0168-9525, 7 p.Article

The ANK3 Bipolar Disorder Gene Regulates Psychiatric-Related Behaviors That Are Modulated by Lithium and StressLEUSSIS, Melanie P; BERRY-SCOTT, Erin M; ROOT, David E et al.Biological psychiatry (1969). 2013, Vol 73, Num 7, pp 683-690, issn 0006-3223, 8 p.Article

Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and DepressionJIE HUANG; PERLIS, Roy H; PURCELL, Shaun et al.The American journal of psychiatry. 2010, Vol 167, Num 10, pp 1254-1263, issn 0002-953X, 10 p.Article

Family-Based Association Study of Lithium-Related and Other Candidate Genes in Bipolar DisorderPERLIS, Roy H; PURCELL, Shaun; FAGERNESS, Jesen et al.Archives of general psychiatry. 2008, Vol 65, Num 1, pp 53-61, issn 0003-990X, 9 p.Article

Non-random mating, parent-of-origin, and maternal―fetal incompatibility effects in schizophreniaKIM, Yunjung; RIPKE, Stephan; KIROV, George et al.Schizophrenia research. 2013, Vol 143, Num 1, pp 11-17, issn 0920-9964, 7 p.Article

zCall: a rare variant caller for array-based genotypingGOLDSTEIN, Jacqueline I; CRENSHAW, Andrew; SCHIZOPHRENIA CONSORTIUM, Swedish et al.Bioinformatics (Oxford. Print). 2012, Vol 28, Num 19, pp 2543-2545, issn 1367-4803, 3 p.Article

Investigation of parent-of-origin effects in ADHD candidate genesJANG WOO KIM; WALDMAN, Irwin D; FARAONE, Stephen V et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2007, Vol 144, Num 6, pp 776-780, issn 1552-4841, 5 p.Article

Absence of association with DAT1 polymorphism and response to methylphenidate in a sample of adults with ADHDMICK, Eric; BIEDERMAN, Joseph; SPENCER, Thomas et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2006, Vol 141, Num 8, pp 890-894, issn 1552-4841, 5 p.Article

Recurrence risks for schizophrenia in a Swedish National CohortLICHTENSTEIN, Paul; BJÖRK, Camilla; HULTMAN, Christina M et al.Psychological medicine (Print). 2006, Vol 36, Num 10, pp 1417-1425, issn 0033-2917, 9 p.Article

Reciprocal Duplication of the Williams-Beuren Syndrome Deletion on Chromosome 7q11.23 Is Associated with SchizophreniaMULLE, Jennifer Gladys; PULVER, Ann E; HURLES, Matthew et al.Biological psychiatry (1969). 2014, Vol 75, Num 5, pp 371-377, issn 0006-3223, 7 p.Article

Disruption of a Large Intergenic Noncoding RNA in Subjects with Neurodevelopmental DisabilitiesTALKOWSKI, Michael E; MAUSSION, Gilles; DIALLO, Alpha B et al.American journal of human genetics. 2012, Vol 91, Num 6, pp 1128-1134, issn 0002-9297, 7 p.Article

PLINK : A tool set for whole-genome association and population-based linkage analysesPURCELL, Shaun; NEALE, Benjamin; SHAM, Pak C et al.American journal of human genetics. 2007, Vol 81, Num 3, pp 559-575, issn 0002-9297, 17 p.Article

Analysis of high-resolution hapmap of DTNBP1 (dysbindin) suggests no consistency between reported common variant associations and schizophreniaMUTSUDDI, Mousumi; MORRIS, Derek W; WAGGONER, Skye G et al.American journal of human genetics. 2006, Vol 79, Num 5, pp 903-909, issn 0002-9297, 7 p.Article

Molecular genetics of attention-deficit/hyperactivity disorderFARAONE, Stephen V; PERLIS, Roy H; DOYLE, Alysa E et al.Biological psychiatry (1969). 2005, Vol 57, Num 11, pp 1313-1323, issn 0006-3223, 11 p.Conference Paper

Implication of a Rare Deletion at Distal 16p11.2 in SchizophreniaGUHA, Saurav; REES, Elliott; CICHON, Sven et al.JAMA psychiatry (Chicago, Ill. Print). 2013, Vol 70, Num 3, pp 253-260, issn 2168-622X, 8 p.Article

Exome sequencing and the genetic basis of complex traitsKIEZUN, Adam; GARIMELLA, Kiran; HULTMAN, Christina M et al.Nature genetics. 2012, Vol 44, Num 6, pp 623-630, issn 1061-4036, 8 p.Article

Linkage Disequilibrium Mlapping of the Chromosome 6q21―22.31 Bipolar I Disorder Susceptibility LocusJINBO FAN; LONITA-LAZA, Iuliana; FRIEDMAN, Edward S et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 1, pp 29-37, issn 1552-4841, 9 p.Article

A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar DisorderPERLIS, Roy H; SMOLLER, Jordan W; SKLAR, Pamela et al.The American journal of psychiatry. 2009, Vol 166, Num 6, pp 718-725, issn 0002-953X, 8 p.Article

Serotonin gene polymorphisms and bipolar I disorder : Focus on the serotonin transporterMANSOUR, Hader A; TALKOWSKI, Michael E; FAGIOLINI, Andrea et al.Annals of medicine (Helsinki). 2005, Vol 37, Num 8, pp 590-602, issn 0785-3890, 13 p.Article

Psychiatric genetics : A survey of Psychiatrists' knowledge, opinions, and practice patternsFINN, Christine T; WILCOX, Marsha A; KORF, Bruce R et al.The Journal of clinical psychiatry. 2005, Vol 66, Num 7, pp 821-830, issn 0160-6689, 10 p.Article

Specific Glial Functions Contribute to Schizophrenia SusceptibilityGOUDRIAAN, Andrea; DE LEEUW, Christiaan; RIPKE, Stephan et al.Schizophrenia bulletin. 2014, Vol 40, Num 4, pp 925-935, issn 0586-7614, 11 p.Article

Extremely low-coverage sequencing and imputation increases power for genome-wide association studiesPASANIUC, Bogdan; ROHLAND, Nadin; SULLIVAN, Patrick F et al.Nature genetics. 2012, Vol 44, Num 6, pp 631-635, issn 1061-4036, 5 p.Article

Analysis of genetic deletions and duplications in the University College London bipolar disorder case control sampleMCQUILLIN, Andrew; BASS, Nicholas; ANJORIN, Adebayo et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 588-592, issn 1018-4813, 5 p.Article

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