Concepedia

Till Stuhlmann

TS

Statistics

Publications

5

Citations

821

H-Index

5

Active since

2013

Affiliations

Max Delbrück Center(Current)

Leibniz-Forschungsinstitut für Molekulare Pharmakologie

Imaging, Brain, and Neuropsychiatry

Centre Hospitalier Universitaire de Tours

Radboud University Nijmegen

Till Stuhlmann is an author at Max Delbrück Center specializing in life sciences, genetics, and exome sequencing.

Publications per year

2013–2020

5

Publications

5

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

Hao Hu, Stefan A. Haas, Jamel Chelly et al. · Molecular Psychiatry · 2015 · 309 citations · Full text

, , +17

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies

Krishna R. Veeramah, Laurel Johnstone, Tatiana M. Karafet et al. · Epilepsia · 2013 · 293 citations · Full text

, , +17

LRRC8/VRAC anion channels enhance β-cell glucose sensing and insulin secretion

Till Stuhlmann, Rosa Planells‐Cases, Thomas J. Jentsch · Nature Communications · 2018 · 97 citations · Full text

, , +12

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

Elizabeth E. Palmer, Till Stuhlmann, Stefanie Weinert et al. · Molecular Psychiatry · 2016 · 72 citations · Full text

, , +17

Uncoupling endosomal CLC chloride/proton exchange causes severe neurodegeneration

Stefanie Weinert, Niclas Gimber, Dorothea Anni Deuschel et al. · The EMBO Journal · 2020 · 50 citations · Full text

, , +13

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