Concepedia

Tobias Willer

TW

Statistics

Publications

31

Citations

3.1K

H-Index

25

Active since

2002

Affiliations

University of Iowa(Current)

Howard Hughes Medical Institute

University College London

Heidelberg University

Inserm

Tobias Willer is an author at University of Iowa specializing in life sciences, genetics, and genetic disorders.

Publications per year

2002–2022

31

Publications

31

A Dystroglycan Mutation Associated with Limb-Girdle Muscular Dystrophy

Yuji Hara, Burcu Balcı-Hayta, Takako Yoshida‐Moriguchi et al. · New England Journal of Medicine · 2011 · 283 citations · Full text

, , +17

Mutations in GDP-Mannose Pyrophosphorylase B Cause Congenital and Limb-Girdle Muscular Dystrophies Associated with Hypoglycosylation of α-Dystroglycan

Keren Carss, Elizabeth Stevens, A. Reghan Foley et al. · The American Journal of Human Genetics · 2013 · 240 citations · Full text

, , +17

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Tobias Willer, Hane Lee, Mark Lommel et al. · Nature Genetics · 2012 · 239 citations · Full text

, , +7

SGK196 Is a Glycosylation-Specific <i>O</i> -Mannose Kinase Required for Dystroglycan Function

Takako Yoshida‐Moriguchi, Tobias Willer, Mary E. Anderson et al. · Science · 2013 · 219 citations · Full text

, , +13

Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of α-Dystroglycan

Elizabeth Stevens, Keren Carss, Sebahattin Çirak et al. · The American Journal of Human Genetics · 2013 · 195 citations · Full text

, , +9

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