Mark D. Ludman

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Duane L. Guernsey, Haiyan Jiang, Dean R. Campagna et al. · Nature Genetics · 2009 · 243 citations

Mendelian Disorder, Genetic Disorder, Genetics +8

Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

Duane L. Guernsey, Haiyan Jiang, Julie Hussin et al. · The American Journal of Human Genetics · 2010 · 194 citations · Full text

Developmental Biology, Cell Division, Molecular Genetics +3

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Duane L. Guernsey, Makoto Matsuoka, Haiyan Jiang et al. · Nature Genetics · 2011 · 171 citations

Allelic Variant, Mendelian Disorder, Genetic Disorder +6

Overlapping spectra of <i>SMAD4</i> mutations in juvenile polyposis (JP) and JP–HHT syndrome

Carol J. Gallione, Arthur S. Aylsworth, Jill Beis et al. · American Journal of Medical Genetics Part A · 2010 · 147 citations

Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in theCOL1A1 andCOL1A2 genes of type I collagen

Peter H. Byers, Madeleine Duvic, Mary Atkinson et al. · American Journal of Medical Genetics · 1997 · 126 citations · Full text