Howard P. Levy

6.8k total citations · 3 hit papers
58 papers, 2.7k citations indexed

About

Howard P. Levy is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Howard P. Levy has authored 58 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Howard P. Levy's work include Connective tissue disorders research (17 papers), BRCA gene mutations in cancer (7 papers) and Genomics and Rare Diseases (4 papers). Howard P. Levy is often cited by papers focused on Connective tissue disorders research (17 papers), BRCA gene mutations in cancer (7 papers) and Genomics and Rare Diseases (4 papers). Howard P. Levy collaborates with scholars based in United States, United Kingdom and Canada. Howard P. Levy's co-authors include Brad T. Tinkle, Rodney Grahame, Marco Castori, Fransiska Malfait, Alan J. Hakim, Helen Cohen, Hanadi Kazkaz, Barbara B. Biesecker, Britta Berglund and Peter S. Rose and has published in prestigious journals such as New England Journal of Medicine, Annals of Internal Medicine and Spine.

In The Last Decade

Howard P. Levy

58 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A framework for the classification of joint hypermobility and related conditions

2017 370 citations Marco Castori, Brad T. Tinkle et al. American Journal of Medical Genetics Part C Seminars in Medical Genetics profile →
Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents

2015 354 citations Yvonne Bombard, Howard P. Levy et al. The American Journal of Human Genetics profile →
Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history

2017 317 citations Brad T. Tinkle, Marco Castori et al. American Journal of Medical Genetics Part C Seminars in Medical Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Howard P. Levy United States	25	1.7k	547	534	298	268	58	2.7k
Kenneth N. Rosenbaum United States	26	1.0k 0.6×	344 0.6×	627 1.2×	244 0.8×	99 0.4×	59	2.2k
Amaka C Offiah United Kingdom	30	748 0.4×	661 1.2×	639 1.2×	769 2.6×	296 1.1×	197	3.4k
Jaime L. Frías United States	34	1.4k 0.8×	879 1.6×	816 1.5×	689 2.3×	287 1.1×	119	3.3k
Helga V. Toriello United States	32	1.4k 0.8×	430 0.8×	1.3k 2.5×	707 2.4×	266 1.0×	97	3.1k
Daniela Larizza Italy	29	1.0k 0.6×	281 0.5×	767 1.4×	299 1.0×	248 0.9×	111	2.4k
Peter Farndon United Kingdom	24	969 0.6×	272 0.5×	1.4k 2.5×	482 1.6×	257 1.0×	63	3.0k
Philippe Backeljauw United States	28	1.4k 0.8×	449 0.8×	1.2k 2.3×	542 1.8×	171 0.6×	118	3.2k
Erica A. Eugster United States	34	1.2k 0.7×	499 0.9×	1.5k 2.7×	383 1.3×	420 1.6×	195	4.2k
Iain McIntosh United States	34	2.4k 1.4×	361 0.7×	1.7k 3.1×	195 0.7×	230 0.9×	83	4.1k
Philip F. Giampietro United States	30	1.4k 0.8×	660 1.2×	1.8k 3.3×	253 0.8×	349 1.3×	89	3.4k

Countries citing papers authored by Howard P. Levy

Since Specialization

Citations

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

Fields of papers citing papers by Howard P. Levy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard P. Levy. 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 Howard P. Levy. The network helps show where Howard P. Levy may publish in the future.

Co-authorship network of co-authors of Howard P. Levy

This figure shows the co-authorship network connecting the top 25 collaborators of Howard P. Levy. A scholar is included among the top collaborators of Howard P. Levy based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Howard P. Levy. Howard P. Levy is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Levy, Howard P., et al.. (2023). Documentation of results and medication prescribing after combinatorial psychiatric pharmacogenetic testing: A case for discrete results. Genetics in Medicine. 26(4). 101056–101056. 3 indexed citations

Miller, Amanda J., Lauren E. Stiles, Rebecca Bascom, et al.. (2020). Prevalence of hypermobile Ehlers-Danlos syndrome in postural orthostatic tachycardia syndrome. Autonomic Neuroscience. 224. 102637–102637. 40 indexed citations

Wolff, Jennifer L., Kimberley Lee, Roisín M. Connolly, et al.. (2019). Sharing in care: engaging care partners in the care and communication of breast cancer patients. Breast Cancer Research and Treatment. 177(1). 127–136. 22 indexed citations

Bombard, Yvonne, Kyle B. Brothers, Sara Fitzgerald‐Butt, et al.. (2019). The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results. The American Journal of Human Genetics. 104(4). 578–595. 77 indexed citations

Tinkle, Brad T. & Howard P. Levy. (2019). Symptomatic Joint Hypermobility. Medical Clinics of North America. 103(6). 1021–1033. 36 indexed citations

Ormond, Kelly E., Miranda L. G. Hallquist, Adam H. Buchanan, et al.. (2018). Developing a conceptual, reproducible, rubric-based approach to consent and result disclosure for genetic testing by clinicians with minimal genetics background. Genetics in Medicine. 21(3). 727–735. 38 indexed citations

Tinkle, Brad T., Marco Castori, Britta Berglund, et al.. (2017). Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 48–69. 317 indexed citations breakdown →

Castori, Marco, Brad T. Tinkle, Howard P. Levy, et al.. (2017). A framework for the classification of joint hypermobility and related conditions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 148–157. 370 indexed citations breakdown →

Li, H. Henry, Paula J. Busse, William R. Lumry, et al.. (2014). Comparison of Chromogenic and ELISA Functional C1 Inhibitor Tests in Diagnosing Hereditary Angioedema. The Journal of Allergy and Clinical Immunology In Practice. 3(2). 200–205. 33 indexed citations

10.

Masys, Daniel R., Gail P. Jarvik, Neil F. Abernethy, et al.. (2011). Technical desiderata for the integration of genomic data into Electronic Health Records. Journal of Biomedical Informatics. 45(3). 419–422. 72 indexed citations

11.

Turriff, Amy, Howard P. Levy, & Barbara B. Biesecker. (2011). Prevalence and psychosocial correlates of depressive symptoms among adolescents and adults with Klinefelter syndrome. Genetics in Medicine. 13(11). 966–972. 52 indexed citations

12.

Butrick, Morgan, Debra Roter, Kimberly A. Kaphingst, et al.. (2011). Patient reactions to personalized medicine vignettes: An experimental design. Genetics in Medicine. 13(5). 421–428. 19 indexed citations

13.

Kline, Antonie D., et al.. (2010). Characterization of sleep disturbance in Cornelia de Lange Syndrome. International Journal of Pediatric Otorhinolaryngology. 75(2). 215–218. 17 indexed citations

14.

Levy, Howard P., et al.. (2008). Twenty questions in genetic medicine—an assessment of World Wide Web databases for genetics information at the point of care. Genetics in Medicine. 10(9). 659–667. 11 indexed citations

15.

Levy, Howard P., et al.. (2008). Perspectives From the Clinic: Will the Average Physician Embrace Personalized Medicine?. Clinical Pharmacology & Therapeutics. 83(3). 492–493. 4 indexed citations

16.

Kline, Antonie D., Marco A. Grados, Paul D. Sponseller, et al.. (2007). Natural history of aging in Cornelia de Lange syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(3). 248–260. 118 indexed citations

17.

Rose, Peter S., Howard P. Levy, Ruth M. Liberfarb, et al.. (2005). Stickler syndrome: Clinical characteristics and diagnostic criteria. American Journal of Medical Genetics Part A. 138A(3). 199–207. 103 indexed citations

18.

Wilkin, Douglas J., Ruth M. Liberfarb, Joie Davis, et al.. (2000). Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: Analysis of potential premature termination codons. American Journal of Medical Genetics. 94(2). 141–148. 17 indexed citations

19.

Kass, Elizabeth M., et al.. (1994). Rickettsialpox in a New York City Hospital, 1980 to 1989. New England Journal of Medicine. 331(24). 1612–1617. 48 indexed citations

20.

Cohen, Maimon M. & Howard P. Levy. (1989). Chromosome Instability Syndromes. PubMed. 18. 43–149. 57 indexed citations

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.

Explore authors with similar magnitude of impact