Kristin Petras

Mutations of <i>ARX</i> are associated with striking pleiotropy and consistent genotype–phenotype correlation

Mitsuhiro Kato, Soma Das, Kristin Petras et al. · Human Mutation · 2004 · 327 citations

Genetics, Pathology, Molecular Genetics +17

Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1–p23.1, 4q21.21–q22.1, 6q26–q27, and 21q2

William B. Dobyns, Ghayda Mirzaa, Susan L. Christian et al. · American Journal of Medical Genetics Part A · 2008 · 174 citations

Clonal evolution underlying leukemia progression and Richter transformation in patients with ibrutinib-relapsed CLL

Sabah Kadri, Jimmy Lee, Carrie Fitzpatrick et al. · Blood Advances · 2017 · 131 citations · Full text

Polyalanine expansion of <i>ARX</i> associated with cryptogenic West syndrome

Mitsuhiro Kato, Soma Das, Kristin Petras et al. · Neurology · 2003 · 100 citations

Age-specific Epilepsy Syndrome, Brain Development, Immunodeficiencies +24

Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia

Eden Haverfield, Amanda J Whited, Kristin Petras et al. · European Journal of Human Genetics · 2008 · 69 citations · Full text

Developmental Biology, Neurobiology Of Disease, Cell Division +9