Sue Kenwrick

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling

Rainer Döffinger, Asma Smahi, Christine Bessia et al. · Nature Genetics · 2001 · 819 citations

Life Sciences, Genetics, Molecular Genetics +13

Cis and trans interactions of L1 with neuropilin‐1 control axonal responses to semaphorin 3A

Valérie Castellani, Elena De Angelis, Sue Kenwrick et al. · The EMBO Journal · 2002 · 216 citations · Full text

Life Sciences, Neurobiology, Neuroscience +10

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

Judith E. Grolleman, Richarda M. de Voer, Fadwa A. Elsayed et al. · Cancer Cell · 2019 · 175 citations · Full text

Medicine, Molecular Biology, Molecular Genetics +12

Mutations in <i>ZIC2</i> in human holoprosencephaly: description of a Novel <i>ZIC2</i> specific phenotype and comprehensive analysis of 157 individuals

B. D. Solomon, Felicitas Lacbawan, Sandra Mercier et al. · Journal of Medical Genetics · 2009 · 85 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Pilot morpholino screen in <i>Xenopus tropicalis</i> identifies a novel gene involved in head development

Sue Kenwrick, Enrique Amaya, Nancy Papalopulu · Developmental Dynamics · 2003 · 52 citations

Life Sciences, Genetics, Molecular Genetics +14