Sansnee Chatkupt

New 19 bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?

William G. Johnson, Edward S. Stenroos, John R. Spychala et al. · American Journal of Medical Genetics Part A · 2003 · 152 citations

Life Sciences, Genetics, Molecular Genetics +15

Clinical manifestations of mitochondria1 DNA depletion

Tuan Vu, Monica Sciacco, Kurenai Tanji et al. · Neurology · 1998 · 127 citations

Life Sciences, Genetics, Neurology +17

Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene

Victor Ionâşescu, Charles Searby, R. Ionasescu et al. · Muscle & Nerve · 1997 · 77 citations

Medicine, Genetics, Neurology +17

PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.

Frans A. Hol, M.P.A. Geurds, Sansnee Chatkupt et al. · Journal of Medical Genetics · 1996 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Parental sex effect in spina bifida: A role for genomic imprinting?

Sansnee Chatkupt, Paul R. Lucek, M. Richard Koenigsberger et al. · American Journal of Medical Genetics · 1992 · 50 citations

Life Sciences, Genetics, Molecular Genetics +14