Davor Lessel - Concepedia

Author

Davor Lessel

University Medical Center Hamburg-Eppendorf ORCID

Also Known As

Azad Razack, D Lessel, D. Lessel, D., Lessel, Davor Lessel, Fowke, J.H., George McMahon, Hadonou, Medard, Joana A. Vidigal, Julian Schulze zur Wiesch

163

Publications

7.8K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Hamburg-Eppendorf Universität Hamburg University of Washington Helmholtz Zentrum München Harvard University

About

Davor Lessel is an author at University Medical Center Hamburg-Eppendorf specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	22	24	1.9K
2	Social Sciences	3	3	218
3	Engineering	1	1	53
4	Public Health	1	1	25
5	Biology	1	1	32

Davor Lessel

Publications

4.3K

Citations

H-Index

Page 1

	Year	Citations
Integrated Molecular Characterization of Testicular Germ Cell Tumors Hui Shen, Juliann Shih, Daniel P. Hollern, Cell Reports	2018	445
Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features Davor Lessel, Bruno Vaz, Swagata Halder, Nature Genetics HepatologyMedicineGeneticsPathologyCancer Genomics	2014	241
Lessons learned from additional research analyses of unsolved clinical exome cases Mohammad K. Eldomery, Zeynep Coban‐Akdemir, Tamar Harel, Genome Medicine	2017	230
Large-scale transcriptome-wide association study identifies new prostate cancer risk regions Nicholas Mancuso, Simon A. Gayther, Alexander Gusev, Nature Communications	2018	171
BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells Davor Lessel, Christina Gehbauer, Nuria C. Bramswig, Brain Bcl11b MutationsBrain DevelopmentLymphocyte DevelopmentGeneticsInnate Lymphoid Cells	2018	132
Recessive mutations in <i>VPS13D</i> cause childhood onset movement disorders Julie Gauthier, Inge A. Meijer, Davor Lessel, Annals of Neurology	2018	128
Shared heritability and functional enrichment across six solid cancers Xia Jiang, Hilary K. Finucane, Fredrick R. Schumacher, Nature Communications	2019	123
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome Jung‐Hyun Kim, Deepali N. Shinde, Margot R.F. Reijnders, The American Journal of Human Genetics Developmental BiologyMendelian DisorderBrain DevelopmentGenetic DisorderGenetics	2016	111
Chromatin retention of DNA damage sensors DDB2 and XPC through loss of p97 segregase causes genotoxicity Marjo-Riitta Puumalainen, Davor Lessel, Peter Rüthemann, Nature Communications ChromatinGenome InstabilityChromatin RetentionDna DamageChromatin Remodeling	2014	107
De Novo Missense Mutations in DHX30 Impair Global Translation and Cause a Neurodevelopmental Disorder Davor Lessel, Claudia Schob, Sébastien Küry, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2017	107

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