(top 60%)
Impact Factor
(top 60%)
extended IF
176(top 1%)
H-Index
1.6K
authors
12.9K
papers
364K
citations
8K
citing journals
61.2K
citing authors

Most Cited Articles of American Journal of Medical Genetics Part A

TitleYearCitations
Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK)19981.4K
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome)20001.1K
Revised diagnostic criteria for the Marfan syndrome19961.1K
Cockayne syndrome: review of 140 cases1992668
Twin studies of schizophrenia: From bow-and-arrow concordances to Star Wars Mx and functional genomics2000639
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination2001594
International Nosology of Heritable Disorders of Connective Tissue, Berlin, 19861988539
Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits2004520
Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion1989492
Endogenous hydrogen sulfide overproduction in Down syndrome2003484
Unusual case of Smith-Lemli-Opitz syndrome "type II"1995484
Prevalence of fragile X syndrome1996477
Genetic variation in the serotonin transporter promoter region affects serotonin uptake in human blood platelets1999470
Prader-Willi syndrome: current understanding of cause and diagnosis1990466
Subclavian artery supply disruption sequence: hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies1986454
Age-related clinical profile of hereditary hemorrhagic telangiectasia in an epidemiologically recruited population1989444
A new genetic concept: uniparental disomy and its potential effect, isodisomy1980442
Analysis of neocortex in three males with the fragile X syndrome1991419
Epidemiology of neurofibromatosis type 11999406
Gardner syndrome in a man with an interstitial deletion of 5q1986405
Diagnostic criteria for Walker-Warburg syndrome1989397
Genetic influences on DSM-III-R drug abuse and dependence: a study of 3,372 twin pairs1996378
D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes2003367
Noonan syndrome: a review1985367
Velo-cardio-facial syndrome: a review of 120 patients1993363