ScholarIQanswers from OpenAlex & ORCID
Gabriel C. Dworschak
ResearcherPublications, citations & collaboration network
Gabriel C. Dworschak is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Gabriel C. Dworschak have?
ScholarIQindexed works
Gabriel C. Dworschak has 46 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Gabriel C. Dworschak have?
ScholarIQcitation count
Gabriel C. Dworschak has 1,649 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Gabriel C. Dworschak?
ScholarIQh-index
Gabriel C. Dworschak has an h-index of 21 in OpenAlex.
What is the i10-index of Gabriel C. Dworschak?
ScholarIQi10-index
Gabriel C. Dworschak has an i10-index of 27 in OpenAlex.
What is the ORCID of Gabriel C. Dworschak?
ScholarIQorcid
The ORCID for Gabriel C. Dworschak is on the source record.
What is the OpenAlex record for Gabriel C. Dworschak?
ScholarIQopenalex
The OpenAlex for Gabriel C. Dworschak is on the source record.
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
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
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
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
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