Jeffrey E. Ming

8.3k total citations · 3 hit papers
68 papers, 5.4k citations indexed

About

Jeffrey E. Ming is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Jeffrey E. Ming has authored 68 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 27 papers in Genetics and 19 papers in Immunology. Recurrent topics in Jeffrey E. Ming's work include Hedgehog Signaling Pathway Studies (17 papers), Immunodeficiency and Autoimmune Disorders (8 papers) and Asthma and respiratory diseases (8 papers). Jeffrey E. Ming is often cited by papers focused on Hedgehog Signaling Pathway Studies (17 papers), Immunodeficiency and Autoimmune Disorders (8 papers) and Asthma and respiratory diseases (8 papers). Jeffrey E. Ming collaborates with scholars based in United States, France and Netherlands. Jeffrey E. Ming's co-authors include Maximilian Muenke, Jennifer D. Hamilton, Allen Radin, Gianluca Pirozzi, Neil M.H. Graham, George D. Yancopoulos, Neil Stahl, Ross E. Rocklin, Erich Roessler and Elaine H. Zackai and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Jeffrey E. Ming

68 papers receiving 5.3k citations

Hit Papers

Dupilumab Treatment in Adults with Moderate-to-Severe Ato... 2013 2026 2017 2021 2014 2013 2014 250 500 750 1000

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeffrey E. Ming United States 28 1.9k 1.6k 1.5k 1.3k 1.2k 68 5.4k
Vorasuk Shotelersuk Thailand 29 1.6k 0.8× 1.1k 0.7× 355 0.2× 252 0.2× 174 0.1× 230 4.3k
Jan Ulrik Prause Denmark 39 1.2k 0.6× 303 0.2× 725 0.5× 542 0.4× 112 0.1× 230 5.1k
Andreas Janecke Austria 37 2.2k 1.2× 1.3k 0.8× 239 0.2× 235 0.2× 172 0.1× 132 4.4k
Masatake Osawa Japan 33 2.2k 1.2× 420 0.3× 324 0.2× 461 0.4× 108 0.1× 92 5.4k
Rosetta Pedotti Italy 27 1.5k 0.8× 374 0.2× 403 0.3× 115 0.1× 265 0.2× 40 4.9k
Rolph Pfundt Netherlands 42 2.6k 1.4× 2.9k 1.9× 191 0.1× 246 0.2× 136 0.1× 136 5.2k
Pietro Luigi Poliani Italy 42 2.1k 1.1× 799 0.5× 501 0.3× 79 0.1× 117 0.1× 145 5.8k
Andrés F. Muro Italy 34 2.1k 1.1× 405 0.3× 382 0.3× 54 0.0× 894 0.8× 91 3.8k
Pamela R. Fain United States 37 1.9k 1.0× 1.4k 0.9× 110 0.1× 295 0.2× 93 0.1× 106 5.3k
Carol Peebles United States 30 1.3k 0.7× 339 0.2× 254 0.2× 222 0.2× 152 0.1× 48 3.8k

Countries citing papers authored by Jeffrey E. Ming

Since Specialization
Citations

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

Fields of papers citing papers by Jeffrey E. Ming

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jeffrey E. Ming. 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 Jeffrey E. Ming. The network helps show where Jeffrey E. Ming may publish in the future.

Co-authorship network of co-authors of Jeffrey E. Ming

This figure shows the co-authorship network connecting the top 25 collaborators of Jeffrey E. Ming. A scholar is included among the top collaborators of Jeffrey E. Ming 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 Jeffrey E. Ming. Jeffrey E. Ming is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Zhang, Huijuan, et al.. (2025). A Comprehensive Review: Advances in Mesenchymal Stem Cell Applications for Burn Wound Repair. Stem Cells International. 2025(1). 6683745–6683745. 1 indexed citations
4.
Kruszka, Paul, Ariel F. Martinez, Jeffrey E. Ming, et al.. (2018). Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(2). 175–186. 3 indexed citations
5.
Beck, Lisa A., Diamant Thaçi, Jennifer D. Hamilton, et al.. (2014). Dupilumab Treatment in Adults with Moderate-to-Severe Atopic Dermatitis. New England Journal of Medicine. 371(2). 130–139. 1008 indexed citations breakdown →
6.
Haldeman‐Englert, Chad, et al.. (2010). A 223-kb De Novo Deletion of PAX9 in a Patient With Oligodontia. Journal of Craniofacial Surgery. 21(3). 837–839. 7 indexed citations
7.
Wong, Dean F., Hiroto Kuwabara, Andrew G. Horti, et al.. (2010). Quantification of cerebral cannabinoid receptors subtype 1 (CB1) in healthy subjects and schizophrenia by the novel PET radioligand [11C]OMAR. NeuroImage. 52(4). 1505–1513. 152 indexed citations
8.
Ming, Jeffrey E. & E. Richard Stiehm. (2008). Genetic Syndromic Immunodeficiencies with Antibody Defects. Immunology and Allergy Clinics of North America. 28(4). 715–736. 6 indexed citations
9.
Ming, Jeffrey E., E. Richard Stiehm, & John M. Graham. (2003). Syndromic Immunodeficiencies: Genetic Syndromes Associated with Immune Abnormalities. Critical Reviews in Clinical Laboratory Sciences. 40(6). 587–642. 23 indexed citations
10.
Ming, Jeffrey E., Erich Roessler, Han G. Brunner, et al.. (2002). Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Human Genetics. 110(4). 297–301. 174 indexed citations
12.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
13.
Ming, Jeffrey E., Erich Roessler, Han G. Brunner, et al.. (2002). Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Human Genetics. 111(4-5). 464–464. 2 indexed citations
14.
Ming, Jeffrey E. & Maximilian Muenke. (2002). Multiple Hits during Early Embryonic Development: Digenic Diseases and Holoprosencephaly. The American Journal of Human Genetics. 71(5). 1017–1032. 233 indexed citations
15.
Russell, Karen, Jeffrey E. Ming, Ketan D. Patel, et al.. (2001). Dominant paternal transmission of Cornelia de Lange syndrome: A new case and review of 25 previously reported familial recurrences. American Journal of Medical Genetics. 104(4). 267–276. 41 indexed citations
17.
Ming, Jeffrey E., Natalie Blagowidow, Joan H.M. Knoll, et al.. (2000). Submicroscopic deletion in cousins with Prader‐Willi syndrome causes a grandmatrilineal inheritance pattern: Effects of imprinting. American Journal of Medical Genetics. 92(1). 19–24. 18 indexed citations
18.
Nanni, Luisa, Jeffrey E. Ming, Maureen Bocian, et al.. (1999). The Mutational Spectrum of the Sonic Hedgehog Gene in Holoprosencephaly: SHH Mutations Cause a Significant Proportion of Autosomal Dominant Holoprosencephaly. Human Molecular Genetics. 8(13). 2479–2488. 274 indexed citations
19.
Ming, Jeffrey E., Donna M. McDonald‐McGinn, Richard I. Markowitz, Eduardo D. Ruchelli, & Elaine H. Zackai. (1997). Heterotaxia in a fetus with campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys: Expanding the phenotype of Cumming syndrome. American Journal of Medical Genetics. 73(4). 419–424. 13 indexed citations
20.
Ming, Jeffrey E., Ralph M. Steinman, & Angela Granelli‐Piperno. (1992). IL-6 enhances the generation of cytolytic T lymphocytes in the allogeneic mixed leucocyte reaction. Clinical & Experimental Immunology. 89(1). 148–153. 25 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.

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