Terry Watnick

8.2k citations
78 papers · 5.3k indexed · 1 hit paper · h-index 41

Impact in

  • Genetics top 0.2%
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
  • Nephrology top 1%
    • Renal Diseases and Glomerulopathies

Papers in

    • Genetic and Kidney Cyst Diseases 73
    • Genetic Syndromes and Imprinting 23
    • Dialysis and Renal Disease Management 5

Terry Watnick

75 papers receiving 5.2k citations

Hit Papers

Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference 2015 · 384 citations
3842015202620182022100200300

Peers

Terry Watnick
Comparison fields: 5 of 112
  • Genetics 4.2k
  • Nephrology 459
  • Pathology and Forensic Medicine 1.1k
  • Molecular Biology 3.5k
  • Sensory Systems 183
Replace Alessandra Boletta with:
Alessandra Boletta Italy
Guanqing Wu United States
Lu W United States
Gregory G. Germino United States
Albrecht Kramer-Zucker Germany
James P. Calvet United States
Carla Rosenberg Brazil
Marjo Kestilä Finland
Andreas Winterpacht Germany
Sami A. Sanjad Lebanon
Terry Watnick relative to Alessandra Boletta Italy Alessandra Boletta's profile →
Citations per field
00.5×3.5×
Alessandra Boletta · 1×
Citations per year

Countries citing papers authored by Terry Watnick

Since Specialization
Citations

This map shows the geographic impact of Terry Watnick's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Terry Watnick with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Terry Watnick more than expected).

Fields of papers citing papers by Terry Watnick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Terry Watnick. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Terry Watnick. The network helps show where Terry Watnick may publish in the future.

Co-authors

The 25 scholars most cited alongside Terry Watnick, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Terry Watnick Line = papers co-authored together Terry Watnick links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown
#Work
1 20241
2 20231
3 20235
4 202252
5 20220
6 20204
7 20192
8 201878
9 201850
10 201895
11 2017123
12 201735
13 20138
14 201046
15 201079
16 2003134
17 2000102
18 199974
19 199875
20 1996469

About Terry Watnick

Terry Watnick is a scholar working on Genetics, Nephrology, Pathology and Forensic Medicine, Molecular Biology and Sensory Systems, having authored 78 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (73 papers), Renal and related cancers (41 papers), Genetic Syndromes and Imprinting (23 papers), Biomedical Research and Pathophysiology (17 papers), Hedgehog Signaling Pathway Studies (9 papers), Renal cell carcinoma treatment (7 papers), Dialysis and Renal Disease Management (5 papers) and Organ Donation and Transplantation (4 papers). The work is most often cited by research in Genetics (4.2k citations), Nephrology (459 citations), Pathology and Forensic Medicine (1.1k citations), Molecular Biology (3.5k citations) and Sensory Systems (183 citations). Terry Watnick has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Gregory G. Germino, Feng Qian, Luiz F. Onuchic, York Pei, Ronald D. Perrone, Vicente E. Torres, Patricia Outeda, Miguel A. García-González, Arlene B. Chapman and Patrick S. Parfrey. Their work appears in journals such as Kidney International, Journal of the American Society of Nephrology, Human Molecular Genetics, Proceedings of the National Academy of Sciences and Nature Communications.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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