Carol A. Wise

12.5k citations

133 papers · 9.8k · 2 hit papers · h-index 48

Impact in

Immunology top 0.5%
- Psoriasis: Treatment and Pathogenesis
- Immune Cell Function and Interaction
Dermatology top 0.5%
- Dermatology and Skin Diseases

Papers in

Genetics 51
- Connective tissue disorders research 33
Molecular Biology 59
- Congenital heart defects research 11
- TGF-β signaling in diseases 9
- RNA and protein synthesis mechanisms 9
- RNA modifications and cancer 7

Co-authors: Pragna I. Patel (5 shared papers)James R. Lupski (4 shared papers)Anne M. Bowcock (6 shared papers)Nitza G. Shoham (2 shared papers)Michael Lovett (8 shared papers)Daniel L. Kastner (2 shared papers)Geryl Wood (2 shared papers)A. Craig Chinault (1 shared paper)
Journals: Nature Genetics (7 papers)Human Molecular Genetics (7 papers)The American Journal of Human Genetics (6 papers)Human Mutation (6 papers)Proceedings of the National Academy of Sciences (4 papers)
Partner nations: United States United Kingdom Japan

In The Last Decade

Carol A. Wise

128 papers receiving 9.5k citations

Carol A. Wise's Hit Papers

align trajectories log scale

Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways 2009 · 1.2k citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2009 Nature Genetics
2008 PLoS Genetics

Peers

Countries citing papers authored by Carol A. Wise

Since Specialization

Citations

This map shows the geographic impact of Carol A. Wise'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 Carol A. Wise with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carol A. Wise more than expected).

Fields of papers citing papers by Carol A. Wise

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carol A. Wise. 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 Carol A. Wise. The network helps show where Carol A. Wise may publish in the future.

Co-authors

The 25 scholars most cited alongside Carol A. Wise, 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 Carol A. Wise Line = papers co-authored together Carol A. Wise links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 133 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways Nature Genetics ·Rajan P. Nair, Kristina Callis Duffin, Cynthia Helms, Jun Ding, Philip E. Stuart, David E. Goldgar, Johann Eli Gudjonsson, Yun Li Hit paper breakdown →	2009	1194
2	A Genome-Wide Association Study of Psoriasis and Psoriatic Arthritis Identifies New Disease Loci PLoS Genetics ·Ying Liu, Cynthia Helms, Wilson J. Liao, Lisa C. Zaba, Shenghui Duan, Jennifer Margaret Gardner, Carol A. Wise, Andrew G. Miner Hit paper breakdown →	2008	566
3	Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome Proceedings of the National Academy of Sciences ·Kim E. Nichols, D. Paul Harkin, Seth Levitz, Michael Krainer, Kathryn Ann Kolquist, Cameo Genovese, Amy Bernard, Martin L. Ferguson	1998	447
4	Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway Proceedings of the National Academy of Sciences ·Nitza G. Shoham, Michael B Centola, Elizabeth A. Mansfield, Keith M. Hull, Geryl Wood, Carol A. Wise, Daniel L. Kastner	2003	415
5	Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder Human Molecular Genetics ·Carol A. Wise	2002	374
6	Charcot–Marie–Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit Nature Genetics ·Carol A. Wise, A. Craig Chinault, Pragna I. Patel, James R. Lupski +1 other	1992	323
7	Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene New England Journal of Medicine ·Benjamin B. Roa, Carlos Alberto Severo Garcia Júnior, Ueli Suter, Deanna A. Kulpa, Carol A. Wise, J.J. Mueller, Andrew A. Welcher, G. Jackson Snipes	1993	302
8	Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis The American Journal of Human Genetics ·Catherine T. Jordan, Li Hua Cao, Elisha D. O. Roberson, Shenghui Duan, Cynthia Helms, Rajan P. Nair, Kristina Callis Duffin, Philip E. Stuart	2012	300
9	Infevers: An evolving mutation database for auto-inflammatory syndromes Human Mutation ·Isabelle Touitou, Suzanne R. Lesage, Michael McDermott, Laurence Cuisset, Hal M. Hoffman, Catherine Dodé, Nitza G. Shoham, Ebun Aganna	2004	272
10	Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A Nature Genetics ·James R. Lupski, Carol A. Wise, Akira Kuwano, Julie T. Parke, Daniel G. Glaze, David H. Ledbetter, Frank Greenberg, Pragna I. Patel +1 other	1992	234
11	The infevers autoinflammatory mutation online registry: update with new genes and functions Human Mutation ·Florian Milhavet, Laurence Cuisset, Hal M. Hoffman, Rima Slim, Hatem El‐Shanti, Ivona A Aksentijevich, Suzanne Lesage, Hans R. Waterham	2008	232
12	Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis Nature Genetics ·Ikuyo Kou, Yohei Takahashi, Todd A. Johnson, Atsushi Takahashi, Long Zhe Guo, Jin Dai, Xusheng Qiu, Swarkar Sharma	2013	224
13	Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases Nature Medicine ·Jin Li, Sihai Dave Zhao, Jonathan P. Bradfield, Frank D. Mentch, Sólrún Melkorka Maggadóttir, Cuiping Hou, Debra J. Abrams, Diana Juhee Chang	2015	196
14	Mutations in the pre-replication complex cause Meier-Gorlin syndrome Nature Genetics ·Louise S. Bicknell, Ernie M.H.F. Bongers, Andrea Leitch, Stephen Brown, Jeroen Schoots, Margaret E Harley, Salim F. Aftimos, Jumana Yousuf Al-Aama	2011	194
15	Blood leukocyte microarrays to diagnose systemic onset juvenile idiopathic arthritis and follow the response to IL-1 blockade The Journal of Experimental Medicine ·Florence Allantaz, Damien Chaussabel, Dorothee Stichweh, Lynda B. Bennett, Windy Allman, Asunción Mejías, Monica I. Ardura, Wendy K. Chung	2007	193
16	Association of TALS Developmental Disorder with Defect in Minor Splicing Component U4atac snRNA Science ·Patrick Edery, Charles Marcaillou, Mourad Sahbatou, Audrey Labalme, Joëlle Chastang, Renaud L. Touraine, Emmanuel Tubacher, Faiza Senni	2011	181
17	Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. PubMed ·Carol A. Wise, Carlos A. Garcia, Stewart N. Davis, Pragna I. Patel, James R. Lupski +2 others	1993	168
18	Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome Nature Genetics ·Louise S. Bicknell, Sarah K. Walker, Anna Klingseisen, Tom Stiff, Andrea Leitch, Claudia Kerzendorfer, Carol-Anne Martin, Patricia Levy Yeyati	2011	158
19	Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes Human Molecular Genetics ·Swarkar Sharma, Xiaochong Gao, Douglas Londoño, Shonn E. Devroy, Kristen Mauldin, Jessica T. Frankel, January Brandon, Dongping Zhang	2011	156
20	Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review Current Genomics ·Elisabeth J. Smith, Florence Allantaz, Lynda B. Bennett, Dongping Zhang, Xiaochong Gao, Geryl Wood, Daniel L. Kastner, Marilynn Punaro	2010	146

About Carol A. Wise

Carol A. Wise is a scholar working on Genetics, Molecular Biology, Immunology, Rheumatology and Pathology and Forensic Medicine, having authored 133 papers that have together received 9.8k indexed citations. Recurring topics across this work include Connective tissue disorders research (33 papers), Scoliosis diagnosis and treatment (22 papers), Genetic factors in colorectal cancer (13 papers), Congenital heart defects research (11 papers), TGF-β signaling in diseases (9 papers), RNA and protein synthesis mechanisms (9 papers), RNA modifications and cancer (7 papers) and Hereditary Neurological Disorders (7 papers). The work is most often cited by research in Immunology (2.9k citations), Dermatology (799 citations), Hematology (849 citations), Rheumatology (1.0k citations) and Genetics (1.9k citations). Carol A. Wise has collaborated with scholars based in United States, United Kingdom and Japan. Frequent co-authors include Pragna I. Patel, James R. Lupski, Anne M. Bowcock, Nitza G. Shoham, Michael Lovett, Daniel L. Kastner, Geryl Wood, A. Craig Chinault, Xiaochong Gao and John A. Herring. Their work appears in journals such as Nature Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Human Mutation and Proceedings of the National Academy of Sciences.

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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Carol A. Wise

Carol A. Wise's Hit Papers

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All Works

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