Author

Manfred Stuhrmann

Medizinische Hochschule Hannover

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:GWAS / association mapping· 2 Organism:human· 2 Approach:statistical model· 2 Assay:GWAS summary statistics· 1

Frequent Co-Authors

Andreas HartmanniD· 2 shared Christel DepienneiD· 2 shared Cornelia Illmann· 2 shared Csaba BartaiD· 2 shared Dongmei YuiD· 2 shared Fotis TsetsosiD· 2 shared Harald Aschauer· 2 shared Johannes HebebrandiD· 2 shared

Activity by Year

2016-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Andreas HartmannORCID

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Synaptic processes and immune-related pathways implicated in Tourette Syndrome

Fotis Tsetsos, Dongmei Yu, Jae Hoon Sul, Alden Y. Huang, Cornelia Illmann, Lisa Osiecki, Sabrina Michelle Darrow, Matthew E. Hirschtritt, Erica Greenberg, Kirsten Müller‐Vahl, Manfred Stuhrmann, Yves Dion, Guy Armand Rouleau, Harald N. Aschauer, Mara Stamenkovic, , Harald Aschauer

This study identifies gene sets associated with Tourette Syndrome using genome-wide data, highlighting synaptic and immune-related pathways.

Translational Psychiatry · Jan 18, 2021Peer-reviewedGenetic & Genomic Medicine

Rare copy number variants in NRXN1 and CNTN6 increase risk for Tourette syndrome

Alden Y Huang, Dongmei Yu, Lea K Davis, Jae-Hoon Sul, Fotis Tsetsos, Vasily Ramensky, Ivette Zelaya, Eliana Marisa Ramos, Lisa Osiecki, Jason A Chen, Lauren M McGrath, Cornelia Illmann, Paul Sandor, Cathy L Barr, Marco Grados, , Danielle C Cath

The paper identifies two rare copy number variants, NRXN1 and CNTN6, significantly increasing the risk of Tourette syndrome in a European ancestry sample.

bioRxiv · Jul 8, 2016Genetics