Kathryn F. Peters

A Mosaic Activating Mutation in <i>AKT1</i> Associated with the Proteus Syndrome

Marjorie J. Lindhurst, Julie C. Sapp, Jamie K. Teer et al. · New England Journal of Medicine · 2011 · 872 citations · Full text

Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Jennifer J. Johnston, Isabelle Olivos‐Glander, Christina Killoran et al. · The American Journal of Human Genetics · 2005 · 276 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10

Process studies in genetic counseling: Peering into the black box

Barbara B. Biesecker, Kathryn F. Peters · American Journal of Medical Genetics · 2001 · 163 citations

Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.

Wendy McKinnon, Bonnie Jeanne Baty, Robin L. Bennett et al. · PubMed · 1997 · 106 citations

Family Medicine, Genetic Testing, Psychiatric Disorders +28

Clinical differentiation between proteus syndrome and hemihyperplasia: Description of a distinct form of hemihyperplasia

Leslie G. Biesecker, Kathryn F. Peters, Thomas N. Darling et al. · American Journal of Medical Genetics · 1998 · 104 citations

Diagnosis, Gynecology, Pathology +17