Gerard Schwartz

Biallelic Mutations in DNAJC12 Cause Hyperphenylalaninemia, Dystonia, and Intellectual Disability

Yair Anikster, Tobias B. Haack, Thierry Vilboux et al. · The American Journal of Human Genetics · 2017 · 155 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Insulin autoantibodies in the pre-diabetic period: Correlation with islet cell antibodies and development of diabetes

B.M. Dean, Frank Becker, J. M. McNally et al. · Diabetologia · 1986 · 122 citations · Full text

Life Sciences, Endocrinology, Immunology +15

Peak bone mass in patients with phenylketonuria

Dalit Modan‐Moses, Iris Vered, Gerard Schwartz et al. · Journal of Inherited Metabolic Disease · 2007 · 115 citations

Medicine, Endocrinology, Orthopedic Surgery +10

A single origin of phenylketonuria in Yemenite Jews

Smadar Avigad, B. E. Cohen, Sofía Bauer et al. · Nature · 1990 · 70 citations

Life Sciences, Genetics, Jewish Studies +4

A DR3-related DX? gene polymorphism strongly associates with insulin-dependent diabetes mellitus

G. A. Hitman, J. A. Sachs, Paul G. Cassell et al. · Immunogenetics · 1986 · 59 citations

Medicine, Genetics, Molecular Genetics +8