W Halliday

Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome

Karen Buysse, Moniek Riemersma, Gareth T. Powell et al. · Human Molecular Genetics · 2013 · 141 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The Degree of Facial Movement following Microvascular Muscle Transfer in Pediatric Facial Reanimation Depends on Donor Motor Nerve Axonal Density

Alison K. Snyder‐Warwick, Adel Fattah, Leanne Zive et al. · Plastic & Reconstructive Surgery · 2015 · 122 citations

Medicine, Maxillofacial Surgery, Plastic Surgery +16

Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.

Tracey Weiler, Cheryl R. Greenberg, Edward Nylen et al. · PubMed · 1996 · 90 citations

Life Sciences, Genetics, Molecular Genetics +12

Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization

Jessie M. Cameron, Valeriy Levandovskiy, Nevena MacKay et al. · Mitochondrion · 2010 · 45 citations

Life Sciences, Cell Biology, Molecular Biology +9

Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci

Tracey Weiler, Cheryl R. Greenberg, Edward Nylen et al. · American Journal of Medical Genetics · 1997 · 18 citations

Life Sciences, Genetics, Molecular Genetics +11