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Gabriel C. Dworschak
ResearcherPublications, citations & collaboration network
Gabriel C. Dworschak is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 46 works, 1,649 citations, an h-index of 21 and an i10-index of 27.
46
Works
1,649
Citations
21
h-index
27
i10-index
How has Gabriel C. Dworschak's publication output changed over time?
ScholarIQpublication output · 2013–2024
Output declined50% over the shown period — from 2 works in 2013 to 1 in 2024.
2
3
3
1
1
20132014201520162024
What are the most-cited papers on Gabriel C. Dworschak?
ScholarIQmost cited works
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, Pawaree Saisawat, Asaf Vivante, Alina C. Hilger, Heiko Reutter, Neveen A. Soliman, Radovan Bogdanović, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt
Kidney International. 2014266 CitationsOPEN ACCESS
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans
Asaf Vivante, Stefan Kohl, Daw‐Yang Hwang, Gabriel C. Dworschak, Friedhelm Hildebrandt
Pediatric Nephrology. 2014231 Citations
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association
Pawaree Saisawat, Stefan Kohl, Alina C. Hilger, Daw‐Yang Hwang, Heon Yung Gee, Gabriel C. Dworschak, Velibor Tasić, Tracie Pennimpede, S. Natarajan, Ethan D. Sperry, Danilo Swann Matassa, Nataša Stajić, Radovan Bogdanović, Ivo de Blaauw, Carlo Marcelis, Charlotte H. W. Wijers, Enrika Bartels, Eberhard Schmiedeke, Dominik Schmidt, Stefanie Märzheuser, Sabine Grasshoff‐Derr, Stefan Holland‐Cunz, Michael Ludwig, Markus M. Nöthen, Markus Draaken, Erwin Brosens, Hugo A. Heij, Dick Tibboel, Bernhard G. Herrmann, Benjamin D. Solomon, Annelies de Klein, Iris A.L.M. van Rooij, Franca Esposito, Heiko Reutter, Friedhelm Hildebrandt
Kidney International. 2013129 CitationsOPEN ACCESS
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, Alina C. Hilger, Pawaree Saisawat, Asaf Vivante, Nataša Stajić, Radovan Bogdanović, Heiko Reutter, Elijah O. Kehinde, Velibor Tasić, Friedhelm Hildebrandt
Journal of the American Society of Nephrology. 2014117 CitationsOPEN ACCESS
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, Asaf Vivante, Stefanie Chan, Gabriel C. Dworschak, Julian Schulz, Albertien M. van Eerde, Alina C. Hilger, Heon Yung Gee, Tracie Pennimpede, Bernhard G. Herrmann, Glenn van de Hoek, Kirsten Y. Renkema, Christoph Schell, Tobias B. Huber, Heiko Reutter, Neveen A. Soliman, Nataša Stajić, Radovan Bogdanović, Elijah O. Kehinde, Richard P. Lifton, Velibor Tasić, Lu W, Friedhelm Hildebrandt
S199832308. 201570 CitationsOPEN ACCESS
Related on ScholarIQ
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract
Paper
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans
Paper
Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association
Paper
Mild Recessive Mutations in Six Fraser Syndrome–Related Genes Cause Isolated Congenital Anomalies of the Kidney and Urinary Tract
Paper
Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract
Paper
Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney disease
Paper