🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Chen‐Han Wilfred Wu

Boston Children's Hospital

ORCID: 0000-0003-4827-9920

Also affiliated with University Hospitals of Cleveland, University of Alabama at Birmingham, Boston Children's Museum, University School, Case Comprehensive Cancer Center, Case Western Reserve University

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 13 papers. Top paper: “Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases”.

Sengers syndrome and AGK-related disorders - Minireview of phenotypic variability and clinical outcomes in molecularly confirmed cases

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107626

N/A

0.425DataRank · unranked

16 citations

Martin Caha, Leslie Smoot, David J. Harris, Amy E. Roberts, Stephanie Sacharow +2 more

Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62644

N/A

0.312DataRank · unranked

7 citations

Steve Seltzsam, Bixia Zheng, Chen‐Han Wilfred Wu, Camille Nicolas‐Frank, Kirollos Yousef +23 more

Recessive CHRM5 variant as a potential cause of neurogenic bladder

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63241

N/A

0.241DataRank · unranked

4 citations

Luca Schierbaum, Wessel A. C. Burger, Steve Seltzsam, Chunyan Wang, Bixia Zheng +13 more

Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs

Journal of the American Society of Nephrology(2022)10.1681/asn.2022010050

N/A

0DataRank · unranked

8 citations

Friedhelm Hildebrandt, Chunyan Wang, Thomas Naert, Karin Richter, Theresa Nauth +28 more

The role of double heterozygotes of SLC3A1 and SLC7A9 in the prevalence of cystine stones

Genetics in Medicine(2024)10.1016/j.gim.2024.101281

N/A

0DataRank · unranked

1 citations

Ishita Patel, Katreya Lovrenert, Brian H. Eisner, Naomi Meeks, Anne Chun‐Hui Tsai +4 more

Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families

Genetics in Medicine(2025)10.1016/j.gim.2025.101432

N/A

0DataRank · unranked

5 citations

Caroline M. Kolvenbach, Chunyan Wang, Nils D. Mertens, Steve Seltzsam, Bshara Mansour +49 more

Increased risk of upper tract urothelial carcinoma in patients with kidney stones: a large-scale analysis of the UK biobank

Urolithiasis(2025)10.1007/s00240-025-01758-5

N/A

0DataRank · unranked

3 citations

Adam Calaway, Sanjay Gupta, Donald R. Bodner, Jason R. Brown, Fredrick R. Schumacher +2 more

Genetic Insights Into Nephrolithiasis and Renal Cancer Predisposition: Precision Medicine in Genes, Diagnosis, and Therapy

Seminars in Nephrology(2025)10.1016/j.semnephrol.2025.151655

N/A

0DataRank · unranked

1 citations

Yu-Ren Mike Huang, Hachem Ziadeh, Bor-En Jong, Prapti Dalal, Hsin-Ti Lin +7 more

Genetic analysis of two bladder exstrophy populations of South Asian and North American origin

Journal of Pediatric Urology(2025)10.1016/j.jpurol.2025.04.018

N/A

0DataRank · unranked

1 citations

Dana Weiß, Austin Thompson, Rakesh Joshi, Jaishri Ramji, Aseem R. Shukla +10 more

Phenotype expansion of heterozygous FOXC1 pathogenic variants toward involvement of congenital anomalies of the kidneys and urinary tract (CAKUT)

Genetics in Medicine(2020)10.1038/s41436-020-0844-z

N/A

0DataRank · unranked

22 citations

Nina Mann, Makiko Nakayama, Dervla M. Connaughton, Rufeng Dai, Caroline M. Kolvenbach +17 more

Isolated multinodular goiter and follicular adenoma associated with a novel germline DICER1 variant: A benign presentation

Cancer Genetics(2025)10.1016/j.cancergen.2025.07.013

N/A

0DataRank · unranked

0 citations

Rachel Rabenn, Aditi Shah Parikh, Chen‐Han Wilfred Wu, Joshua C. Chang

Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract

Nephrology Dialysis Transplantation(2021)10.1093/ndt/gfab253

N/A

0DataRank · unranked

11 citations

Steve Seltzsam, Chunyan Wang, Luca Schierbaum, Sophia Schneider, Chen‐Han Wilfred Wu +12 more

Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract

European Urology Open Science(2022)10.1016/j.euros.2022.08.004

N/A

0DataRank · unranked

12 citations

Tze Yin Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum +31 more