H. J. M. Smeets

Normal phenotype in two brothers with a full FMR1 mutation

H. J. M. Smeets, Anne Smits, Coleta Verheij et al. · Human Molecular Genetics · 1995 · 178 citations

Epigenetic Change, Genetics, Pathology +17

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

E.J. Meijers-Heijboer, L. Sandkuijl, Han G. Brunner et al. · Journal of Medical Genetics · 1992 · 50 citations · Full text

Genetics, Molecular Genetics, Genomic Imprinting +16

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers

Marion Drüsedau, Jos Dreesen, I. A. P. Derks-Smeets et al. · European Journal of Human Genetics · 2013 · 23 citations · Full text

Universal Tests, Breast Oncology, Medicine +11

Different distribution of the genetic subtypes of the Prader–Willi syndrome in the elderly

Margje Sinnema, Kees E. P. van Roozendaal, Marian A. Maaskant et al. · European Journal of Human Genetics · 2010 · 13 citations · Full text

Genetic Subtypes, Clinical Genetic Disorders, Genetic Disorder +13

Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors

Nicole Y. Souren, Aimée Paulussen, Anja Steyls et al. · International Journal of Obesity · 2009 · 13 citations

Obesity, Metabolic Syndrome, Growth Hormone +9