S
Stephen V. Faraone
Researcher at State University of New York Upstate Medical University
Publications - 1470
Citations - 155368
Stephen V. Faraone is an academic researcher from State University of New York Upstate Medical University. The author has contributed to research in topics: Attention deficit hyperactivity disorder & Bipolar disorder. The author has an hindex of 188, co-authored 1427 publications receiving 140298 citations. Previous affiliations of Stephen V. Faraone include University of Bergen & National Institute for Health Research.
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Meta-analysis of data from the Psychiatric Genomics Consortium and additional samples supports association of CACNA1C with risk for schizophrenia.
Sakae Takahashi,Stephen J. Glatt,Makoto Uchiyama,Stephen V. Faraone,Ming T. Tsuang,Ming T. Tsuang +5 more
TL;DR: This study followed up on top GWAS hits by genotyping implicated loci in additional schizophrenia family samples from the Psychiatric Genomics Consortium by meta-analysis, and found that the well replicated results from the PGC hold up in new samples, and may suggest that the top hits are generalizable, even to other ancestral groups.
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Re-examining the risk for switch from unipolar to bipolar major depressive disorder in youth with ADHD: a long term prospective longitudinal controlled study.
Joseph Biederman,Janet Wozniak,Laura Tarko,Giulia Serra,Mariely Hernandez,Katie McDermott,K. Yvonne Woodsworth,Mai Uchida,Stephen V. Faraone +8 more
TL;DR: Switches from unipolar MDD to BP-I disorder in children with ADHD and MDD were predicted by baseline subthreshold BP- I disorder symptoms and baseline deficits in emotional regulation.
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Autism spectrum disorder traits in Slc9a9 knock-out mice
TL;DR: This study provides strong evidence that lack of Slc9a9 leads to ASD‐like behaviors in mice and provides the field with a new mouse model of ASDs.
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Genetic counseling for psychiatric disorders.
TL;DR: The principles of genetic counseling for psychiatric disorders are reviewed, as well as the social and ethical dilemmas that genetic testing may bring.
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Family-based association study of SELENBP1 in schizophrenia.
Tetsufumi Kanazawa,Stephen J. Glatt,Stephen V. Faraone,Hai-Gwo Hwu,Hiroshi Yoneda,Ming T. Tsuang,Ming T. Tsuang,Ming T. Tsuang +7 more
TL;DR: One of four haplotype-tagging SNPs and two different two-marker haplotypes showed nominally significant evidence for association with schizophrenia under an additive model, suggesting that genetic variation in SELENBP1 may influence risk for the disorder.