Gabriel C. Dworschak

Author

Also Known As

G Dworschak, G. Dworschak, G.C. Dworschak, GABRIEL C. DWORSCHAK, Gabriel C Dworschak, Gabriel C. Dworschak, Gabriel Clemens Dworschak, Gabriel Dworschak, Stephanie Geitmann

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

University Hospital Bonn University of Bonn Harvard University Boston Children's Hospital Heidelberg University

About

Gabriel C. Dworschak is an author at University Hospital Bonn specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	469
2	Engineering	1	1	41
3	Natural Sciences	1	1	127
4	Biology	1	1	127
5	Immunology	1	1	55

Gabriel C. Dworschak

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract Daw‐Yang Hwang, Gabriel C. Dworschak, Stefan Kohl, Kidney International	2014	256
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association Pawaree Saisawat, Stefan Kohl, Alina C. Hilger, Kidney International BiologyGenetic DisorderNatural SciencesGeneticsVacterl Association	2013	127
Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Journal of the American Society of Nephrology GeneticsRenal PathologyPathologyMolecular GeneticsDisease Gene Identification	2014	108
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract Daw‐Yang Hwang, Stefan Kohl, Xueping Fan, Human Genetics UrologyDevelopmental BiologyMolecular PhysiologyUrinary TractGenetics	2015	67
De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL‐like association and analysis of <i>EFNB2</i> in patients with anorectal malformations Gabriel C. Dworschak, Markus Draaken, Carlo Marcelis, American Journal of Medical Genetics Part A	2013	66
Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease Roslyn Simms, Kah Mean Thong, Gabriel C. Dworschak, Nephrology Dialysis Transplantation	2015	63
Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate<i>ZIC3</i>and<i>FOXF1</i>in Human VATER/VACTERL Association Alina C. Hilger, Jan Halbritter, Tracie Pennimpede, Human Mutation GeneticsImmunologyGenomic MechanismPathologyGene Characterization	2015	55
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations Dervla M. Connaughton, Rufeng Dai, Danielle Owen, The American Journal of Human Genetics MedicineGeneticsDevelopmental BiologyNeurogenetics	2020	49
Rare Variants in BNC2 Are Implicated in Autosomal-Dominant Congenital Lower Urinary-Tract Obstruction Caroline M. Kolvenbach, Gabriel C. Dworschak, Sandra Frese, The American Journal of Human Genetics	2019	44
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association Alina C. Hilger, Charlotte Schramm, Tracie Pennimpede, European Journal of Human Genetics EngineeringMedicinePathogenesisPathologyVirology	2013	41

Page 1