Galen M. Schauer

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

Frank Rutsch, Nico Ruf, Sucheta M. Vaingankar et al. · Nature Genetics · 2003 · 603 citations

Life Sciences, Genetics, Molecular Genetics +8

Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway

Justyna A. Karolak, Marie Vincent, Gail Deutsch et al. · The American Journal of Human Genetics · 2019 · 183 citations · Full text

Life Sciences, Developmental Biology, Genetics +15

Neuronal loss in Pelizaeus–Merzbacher disease differs in various mutations of the proteolipid protein 1

Anders A. F. Sima, Christopher R. Pierson, Randall L. Woltjer et al. · Acta Neuropathologica · 2009 · 48 citations · Full text

Life Sciences, Genetics, Neuroscience +11

Craniosynostosis: Another feature of the 22q11.2 deletion syndrome

Donna M. McDonald‐McGinn, Karen W. Gripp, Richard E. Kirschner et al. · American Journal of Medical Genetics Part A · 2005 · 45 citations

Medicine, Surgery, Craniofacial Development +11

Facial Infiltrating Lipomatosis

Jieon Kim, Joshua A. Gottschall, Ronald Bachman et al. · Archives of Otolaryngology - Head and Neck Surgery · 2010 · 30 citations

Dentistry, Oral Pathology, Oral Radiology +14