Alexander Münchau

Also affiliated with University of Lübeck

PsychologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD”.

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Nature Communications(2023)10.1038/s41467-023-43776-0

N/A

0.657DataRank · unranked

24 citations

Belinda Wang, Vanessa Drury, Sam Drake, Nawei Sun, Hasan Alkhairo +63 more

Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome

Biological Psychiatry(2023)10.1016/j.biopsych.2023.01.023

N/A

0.520DataRank · unranked

31 citations

Apostolia Topaloudi, Pritesh Jain, Zhiyu Yang, Dongmei Yu, Petros Kolovos +94 more

Investigation of gene–environment interactions in relation to tic severity

Journal of Neural Transmission(2021)10.1007/s00702-021-02396-y

N/A

0DataRank · unranked

9 citations

Dongmei Yu, Lisa Osiecki, Robert A. King, Thomas Fernandez, Lawrence W. Brown +36 more

Investigation of gene-environment interactions in relation to tic severity

medRxiv(2021)10.1101/2021.05.12.21257005

N/A

0DataRank · unranked

0 citations

Dongmei Yu, Lisa Osiecki, Robert A. King, Thomas Fernandez, Lawrence W. Brown +36 more

Enhancing neuroimaging genetics through meta-analysis for Tourette syndrome (ENIGMA-TS): A worldwide platform for collaboration

Frontiers in Psychiatry(2022)10.3389/fpsyt.2022.958688

N/A

0DataRank · unranked

11 citations

Yin Jin, Kirsten Müller‐Vahl, Harald E. Möller, Renata Rizzo, Pieter J. Hoekstra +56 more

Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome

medRxiv(2022)10.1101/2022.09.01.22279340

N/A

0DataRank · unranked

3 citations

Tyne W. Miller‐Fleming, Apostolia Topaloudi, Dongmei Yu, Petros Drineas, Marianthi Georgitsi +46 more

Transitional Care for Young People with Movement Disorders: Consensus‐Based Recommendations from the MDS Task Force on Pediatrics

Movement Disorders Clinical Practice(2023)10.1002/mdc3.13728

N/A

0DataRank · unranked

10 citations

Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi‐Fakhari +18 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

Genetic Risk Factors in Isolated Dystonia Escape Genome‐Wide Association Studies

Movement Disorders(2024)10.1002/mds.29968

N/A

0DataRank · unranked

4 citations

Katja Lohmann, Eva‐Juliane Vollstedt, Tobias Reinberger, Lisa‐Marie Nuxoll, Gamze Kilic‐Berkmen +53 more

Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree

Molecular Psychiatry(2021)10.1038/s41380-021-01277-w

N/A

0DataRank · unranked

10 citations

Jin Szatkiewicz, Poorva Mudgal, Dongmei Yu, H.N. Aschauer, Gil Atzmon +94 more