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International Journal of Adolescent Medicine and Health|October 20, 2005
Family-based association study of 5-HT(2A) receptor T102C polymorphism and suicidal behavior in Ashkenazi inpatient adolescentsGil Zalsman, Amos Frisch, Ruth Baruch-Movshovits, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|September 25, 2004
CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish populationMaya Koronyo-Hamaoui, Eva Gak, Daniel Stein, et al.
Psychiatric Genetics|June 2, 2017
Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindredNadine M Melhem, Sami Hamdan, Lambertus Klei, et al.
Journal of Psychiatric Research|September 15, 2005
Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosaMaya Koronyo-Hamaoui, Amos Frisch, Daniel Stein, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|August 16, 2016
Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndromeRonnie Weinberger, James Yi, Monica Calkins, et al.
European Child & Adolescent Psychiatry|July 17, 2025
Early developmental milestones associated with tics and psychopathological comorbidity: An EMTICS studyTamar Steinberg, Dana Feldman-Sadeh, Alan Apter, et al.
Circulation. Cardiovascular Genetics|October 14, 2017
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3Tingwei Guo, Gabriela M Repetto, Donna M McDonald McGinn, et al.
Medrxiv : the Preprint Server for Health Sciences|March 27, 2026
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndromeJhih-Rong Lin, Daniella Miller, Dana Luong, et al.
Molecular Psychiatry|February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionIsabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
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