Clair A. Francomano

17.7k citations

168 papers · 11.0k indexed · 1 hit paper · h-index 54

Impact in

Genetics top 0.1%
- Connective tissue disorders research
- Craniofacial Disorders and Treatments
Rheumatology top 0.2%
- Osteoarthritis Treatment and Mechanisms

Papers in

Genetics 111
- Connective tissue disorders research 94
- Dermatological and Skeletal Disorders 17
Immunology and Allergy 15
- Cell Adhesion Molecules Research 15

Co-authors: Reed E. Pyeritz Harry C. Dietz Iain McIntosh Jacqueline T. Hecht Deborah A. Meyers Glen M. Corson Lynn Y. Sakai Gary A. Bellus
Journals: American Journal of Medical Genetics Part C Seminars in Medical Genetics (13 papers)Genomics (11 papers)Nature Genetics (8 papers)The American Journal of Human Genetics (6 papers)Human Genetics (5 papers)
Partner nations: United States United Kingdom Finland

In The Last Decade

Clair A. Francomano

164 papers receiving 10.7k citations

Hit Papers

align trajectories log scale

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene 1991 · 1.5k citations

Peers

Countries citing papers authored by Clair A. Francomano

Since Specialization

Citations

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

Fields of papers citing papers by Clair A. Francomano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Patient interest in the development of a center for Ehlers-Danlos syndrome/hypermobility spectrum disorder in the Chicagoland region Orphanet Journal of Rare Diseases ·Wendy Wagner, Я.В. Зайцев, Clair A. Francomano, Dacre Knight, Colin Halverson	2024	2
2	Assessment of gait mechanics and muscle strength in hypermobile Ehlers Danlos Syndrome Clinical Biomechanics ·Kaname, Didson Harvey Sánchez Monroy, Christopher J. McLouth, Jody L. Clasey, Clair A. Francomano, Bryan Paúl Rodríguez Lloré, Michael A. Samaan	2024	3
3	P168: Nutritional markers of histamine intolerance in Ehlers-Danlos syndromes SHILAP Revista de lepidopterología ·Y Jiang, Катерина Миколаївна Муліка, 正秀金子, Anne Maitland, Jane R. Schubart, Clair A. Francomano	2023	0
4	Comorbidity, misdiagnoses, and the diagnostic odyssey in patients with hypermobile Ehlers-Danlos syndrome SHILAP Revista de lepidopterología ·Colin Halverson, Sha Cao, Susan M. Perkins, Clair A. Francomano	2023	21
5	Effects of hypermobile Ehlers‐Danlos syndrome patients on the workflow and professional satisfaction of genetic counselors Journal of Genetic Counseling ·Я. А. Кулигина, Benjamin M. Helm, Roland Barthes, Clair A. Francomano, Colin Halverson	2023	4
6	Use of prescription opioid and other drugs among a cohort of persons with Ehlers–Danlos syndrome: A retrospective study American Journal of Medical Genetics Part A ·Jane R. Schubart, Amber Schilling, Élise Schaefer, Rebecca Bascom, Clair A. Francomano	2019	18
7	Characteristics, Diagnosis, and Management of Ehlers-Danlos Syndromes JAMA Facial Plastic Surgery ·Andrew W. Joseph, 正春和田, Clair A. Francomano, Theda C. Kontis	2017	36
8	Pain management in the Ehlers–Danlos syndromes American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Pradeep Chopra, Brad T. Tinkle, C. Hamonet, 正秀金子, Anne Gompel, Antonio Bulbena, Clair A. Francomano	2017	122
9	Complementary Medicine and Genetic Medicine: Polar Disciplines or Dynamic Partners? The Journal of Alternative and Complementary Medicine ·Gail Geller, Clair A. Francomano	2005	3
10	Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis Nature Genetics ·Víctor L. Ruiz‐Pérez, Susan Ide, Tim M. Strom, Bettina Lorenz, David I. Wilson, Kathryn Woods‐Townsend, Lynn King, Clair A. Francomano, Peter Freisinger, Stephanie Spranger, Bruno Marino, Bruno Dallapiccola, Michael Wright, Thomas Meitinger, Mihael H. Polymeropoulos, Judith Goodship	2000	224
11	Mutations in Fibroblast Growth-Factor Receptor 3 in Sporadic Cases of Achondroplasia Occur Exclusively on the Paternally Derived Chromosome The American Journal of Human Genetics ·Douglas J. Wilkin, Joseph ShunFeng WEN, Rhoda Cameron, Shirley Henderson, Gary A. Bellus, Michelle Mack, Ilkka Kaitila, John Loughlin, Arnold Münnich, Bryan Sykes, Jacky Bonaventure, Clair A. Francomano	1998	160
12	Physical mapping of the nail patella syndrome interval at 9q34: ordering of STSs and ESTs Human Genetics ·Wafaa Eyaid, Mark V. Clough, Zulfatus Sholikah, Kathleen M. Scott, Mary Kay McCormick, Adhiziti Naluriannisa Edya Nugraha, Н. А. Лисицын, W.G. Kearns, Clair A. Francomano, Julia E. Richards, Iain McIntosh	1998	4
13	Bone dysplasias in man: molecular insights Current Opinion in Genetics & Development ·Clair A. Francomano, Iain McIntosh, Douglas J. Wilkin	1996	37
14	Hypochondroplasia: Molecular Analysis of the Fibroblast Growth Factor Receptor 3 Gene Annals of the New York Academy of Sciences ·Gary A. Bellus, Iain McIntosh, Joseph ShunFeng WEN, Arthur S. Aylsworth, Ilkka Kaitila, Clair A. Francomano	1996	20
15	A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis. Genome Research ·M R Johnson, M H Polymeropoulos, Hans L. Vos, Rosa Isela Ortiz De Luna, Clair A. Francomano	1996	106
16	Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model American Journal of Medical Genetics ·Maria Karayiorgou, Laura Kasch, Virginia K. Lasseter, Jennifer Hwang, Ramu Elango, Mohd Fairuz Zamani, Michelle L. Kimberland, Robert Babb, Clair A. Francomano, Paula Wolyniec, Malgorzata Lamacz, Gerald Nestadt, Deborah A. Meyers, Jürg Ott, Barton Childs, Stylianos E. Antonarakis, Haig H. Kazazian, David E. Housman, Ann E. Pulver	1994	18
17	Linkage of typical pseudoachondroplasia to chromosome 19 Genomics ·Jacqueline T. Hecht, Clair A. Francomano, Michael D. Briggs, Michelle Deere, Valentin Belissen, William A. Horton, Matthew L. Warman, Daniel H. Cohn, Susan H. Blanton	1993	43
18	PCR-based detection of polymorphicDdel andKpnl sites in intron 5 of the adenylate kinase (AK1) gene Nucleic Acids Research ·Erik G. Puffenberger, Clair A. Francomano	1991	2
19	Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria The Journal of Pediatrics ·Dennis W. Bartholomew, Mark L. Batshaw, Robert H. Allen, Charles R. Roe, David S. Rosenblatt, David Valle, Clair A. Francomano	1988	55
20	Achondropiasia is not caused by mutation in the gene for type II collagen American Journal of Medical Genetics ·Clair A. Francomano, Reed E. Pyeritz, John M. Optiz, James F. Reynolds	1988	11

About Clair A. Francomano

Clair A. Francomano is a scholar working on Genetics, Immunology and Allergy, Rheumatology, Genetics and Clinical Biochemistry, having authored 168 papers that have together received 11.0k indexed citations. Recurring topics across this work include Connective tissue disorders research (94 papers), Dermatological and Skeletal Disorders (17 papers), Dupuytren's Contracture and Treatments (15 papers), Cell Adhesion Molecules Research (15 papers), Osteoarthritis Treatment and Mechanisms (10 papers), Spinal Dysraphism and Malformations (9 papers), Spinal Fractures and Fixation Techniques (9 papers) and Fibroblast Growth Factor Research (9 papers). The work is most often cited by research in Genetics (6.2k citations), Rheumatology (1.8k citations), Immunology and Allergy (682 citations), Cancer Research (1.0k citations) and Developmental Biology (134 citations). Clair A. Francomano has collaborated with scholars based in United States, United Kingdom and Finland. Frequent co-authors include Reed E. Pyeritz, Harry C. Dietz, Iain McIntosh, Jacqueline T. Hecht, Deborah A. Meyers, Glen M. Corson, Lynn Y. Sakai, Gary A. Bellus, Douglas J. Wilkin and Erik G. Puffenberger. Their work appears in journals such as American Journal of Medical Genetics Part C Seminars in Medical Genetics, Genomics, Nature Genetics, The American Journal of Human Genetics and Human Genetics.

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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