Johannes Schumacher - Concepedia

Author

Johannes Schumacher

Also Known As

Aaron P. Thrift, Carlo Maj, Eric Fombonne, J Schumacher, J. SCHUMACHER, J. Schumacher, Johannes Schumacher, Johannes H. Smit, Jörg Schumacher, Schumacher, Johannes

212

Publications

11.2K

Citations

H-Index

156

Concepts

All Affiliations

University of Bonn Life & Brain (Germany)Philipps University of Marburg University Hospital Bonn Max Planck Institute of Psychiatry

About

Johannes Schumacher is an author at University of Bonn specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	40	4.6K
2	Education	2	2	85
3	Engineering	1	1	16
4	Language Studies	1	1	41
5	Natural Sciences	1	1	16

Johannes Schumacher

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations Sarah Kim-Hellmuth, Matthias Bechheim, Benno Pütz, Nature Communications Disease EtiologyGeneticsImmunologyGenetic EpidemiologyImmune Regulation	2017	248
Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q Matthew B. McQueen, Bernie Devlin, Stephen V. Faraone, The American Journal of Human Genetics Linkage DisequilibriumPsychiatryEleven Linkage StudiesChromosomes 6QGenetics	2005	244
Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia Johannes Schumacher, Heidi Anthoni, Faten Dahdouh, The American Journal of Human Genetics Neurodevelopmental DisordersMolecular NeuroscienceCorticobasal DegenerationStrong Genetic EvidenceGenetic Disorder	2005	238
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8 Kym M. Boycott, Chandree L. Beaulieu, Kristin D. Kernohan, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderAutosomal-recessive Intellectual DisabilityGenetic DisorderGenetics	2015	224
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases Tobias L. Lenz, Aaron J. Deutsch, Buhm Han, Nature Genetics HistocompatibilityHlaImmunogeneticsAllergyHuman Leukocyte Antigen	2015	202
Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heterogeneity in reflux diagnosis Jue‐Sheng Ong, Jiyuan An, Xikun Han, Gut	2021	179
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection Marco Henneke, Simone Diekmann, Andreas Ohlenbusch, Nature Genetics NeurovirologyMedicinePathogenesisImmunologyPathology	2009	151
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber, Molecular Psychiatry	2020	127
Comparison of Neoadjuvant Nab-Paclitaxel+Carboplatin vs Nab-Paclitaxel+Gemcitabine in Triple-Negative Breast Cancer: Randomized WSG-ADAPT-TN Trial Results Oleg Gluz, Ulrike Nitz, Cornelia Liedtke, JNCI Journal of the National Cancer Institute	2017	122

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