Tobias Moll

University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN)

385a Glossop Road

Sheffield

United Kingdom

SCHOLARLY PAPERS

2

DOWNLOADS

38

SSRN CITATIONS

0

CROSSREF CITATIONS

1

Scholarly Papers (2)

1.

Rare Variant Burden Analysis within Enhancers Identifies CAV1 as a New ALS Risk Gene

Number of pages: 38 Posted: 11 Jun 2020
University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), Stanford University - Stanford Center for Genomics and Personalized Medicine, University of Massachusetts Worcester - Department of Neurology, University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), Weizmann Institute of Science - Department of Molecular Genetics, Weizmann Institute of Science - Department of Molecular Genetics, Weizmann Institute of Science - Department of Molecular Genetics, Lund University - Department of Biology, University of Sheffield - Sheffield Institute for Nucleic Acids (SInFoNiA), University of Sheffield - Sheffield Institute for Nucleic Acids (SInFoNiA), Massachusetts General Hospital and Harvard Medical School - Analytic and Translational Genetics Unit, Weizmann Institute of Science - Department of Molecular Genetics, Weizmann Institute of Science - Department of Molecular Genetics, University of Southampton - Faculty of Medicine, Health and Life Sciences, King's College London - Maurice Wohl Clinical Neuroscience Institute, King’s College London - Institute of Psychiatry, Psychology and Neuroscience, affiliation not provided to SSRN, Utrecht University - Department of Neurology, University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), Stanford University - Stanford Center for Genomics and Personalized Medicine and University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN)
Downloads 26 (594,587)
Citation 1

Abstract:

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Amyotrophic lateral sclerosis, whole genome sequencing, CAV1, CAV2, noncoding DNA

2.

Genome-Wide Identification of the Genetic Basis of Amyotrophic Lateral Sclerosis

Number of pages: 71 Posted: 07 Dec 2020
Stanford University - Stanford Center for Genomics and Personalized Medicine, University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), Stanford University - Department of Genetics, Stanford University - Department of Genetics, University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of California, San Francisco (UCSF) - Department of Neurology, University of California, San Francisco (UCSF) - Department of Neurology, Weizmann Institute of Science - Department of Molecular Genetics, Weizmann Institute of Science - Department of Molecular Genetics, University Medical Center Utrecht - Department of Neurology, affiliation not provided to SSRN, Utrecht University - Department of Neurology, University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN), University of Sheffield - Sheffield Institute for Translational Neuroscience (SITraN) and Stanford University - Stanford Center for Genomics and Personalized Medicine
Downloads 12 (694,511)

Abstract:

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