Philippe M. Frossard

3.6k total citations
70 papers, 1.4k citations indexed

About

Philippe M. Frossard is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Philippe M. Frossard has authored 70 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Genetics and 16 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Philippe M. Frossard's work include Genetic Associations and Epidemiology (13 papers), Cystic Fibrosis Research Advances (11 papers) and Hormonal Regulation and Hypertension (10 papers). Philippe M. Frossard is often cited by papers focused on Genetic Associations and Epidemiology (13 papers), Cystic Fibrosis Research Advances (11 papers) and Hormonal Regulation and Hypertension (10 papers). Philippe M. Frossard collaborates with scholars based in United Arab Emirates, Pakistan and United States. Philippe M. Frossard's co-authors include Gilles G. Lestringant, K. P. Dawson, Danish Saleheen, G.G. Lestringant, Saman K. Hashmi, Juliette Faraco, Andrew J. Baker, Aisha Ambreen, John Shine and Mohammad Ishaq and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Hypertension.

In The Last Decade

Philippe M. Frossard

70 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philippe M. Frossard United Arab Emirates 21 390 361 305 271 240 70 1.4k
Ligong Chen United States 20 392 1.0× 124 0.3× 75 0.2× 429 1.6× 380 1.6× 59 1.5k
N. J. Samani United Kingdom 15 559 1.4× 178 0.5× 108 0.4× 196 0.7× 184 0.8× 37 1.1k
Tiina Heliö Finland 24 1.3k 3.2× 70 0.2× 411 1.3× 650 2.4× 316 1.3× 77 2.2k
Joachim Kreuder Germany 19 185 0.5× 59 0.2× 61 0.2× 508 1.9× 194 0.8× 53 1.4k
James Schwartz United States 13 176 0.5× 601 1.7× 139 0.5× 359 1.3× 225 0.9× 26 1.3k
Stella Bernardi Italy 27 446 1.1× 846 2.3× 100 0.3× 595 2.2× 621 2.6× 91 2.1k
V. Kerlan France 18 70 0.2× 786 2.2× 450 1.5× 277 1.0× 342 1.4× 90 1.6k
Agnieszka Szadkowska Poland 22 120 0.3× 1.1k 3.0× 868 2.8× 225 0.8× 770 3.2× 147 1.9k
Paul Ryan United Kingdom 20 44 0.1× 169 0.5× 271 0.9× 263 1.0× 212 0.9× 36 1.3k

Countries citing papers authored by Philippe M. Frossard

Since Specialization
Citations

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

Fields of papers citing papers by Philippe M. Frossard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philippe M. Frossard. 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 Philippe M. Frossard. The network helps show where Philippe M. Frossard may publish in the future.

Co-authorship network of co-authors of Philippe M. Frossard

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe M. Frossard. A scholar is included among the top collaborators of Philippe M. Frossard 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 Philippe M. Frossard. Philippe M. Frossard 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.
Jeeva, Irfan, et al.. (2007). Atypical Takayasu arteritis: a family with five affected siblings.. PubMed. 13(4). 59–5. 6 indexed citations
2.
Saleheen, Danish, et al.. (2005). Strong Association of a Renin Intronic Dimorphism with Essential Hypertension. Hypertension Research. 28(4). 339–344. 23 indexed citations
3.
Lestringant, G.G., et al.. (2004). Xeroderma Pigmentosum in Four Siblings With Three Different Types of Malignancies Simultaneously in One. Journal of Pediatric Hematology/Oncology. 26(8). 473–475. 5 indexed citations
4.
Iqbal, Mohammad Perwaiz & Philippe M. Frossard. (2003). Methylene tetrahydrofolate reductase gene and coronary artery disease.. PubMed. 53(1). 33–6. 8 indexed citations
5.
Sprecher, Eli, Gilles G. Lestringant, Raymonde Szargel, et al.. (2000). Reply. Journal of Investigative Dermatology. 115(4). 762–763. 2 indexed citations
6.
Dawson, K. P. & Philippe M. Frossard. (2000). The geographic distribution of cystic fibrosis mutations gives clues about population origins. European Journal of Pediatrics. 159(7). 496–499. 25 indexed citations
7.
Lestringant, Gilles G., et al.. (1999). Allergic contact dermatitis in the United Arab Emirates. International Journal of Dermatology. 38(3). 181–186. 20 indexed citations
8.
Frossard, Philippe M., Gilles G. Lestringant, Mary J. Malloy, & John P. Kane. (1999). Human renin gene BglI dimorphism associated with hypertension in two independent populations. Clinical Genetics. 56(6). 428–433. 30 indexed citations
9.
Frossard, Philippe M. & Gilles G. Lestringant. (1999). Analysis of the Apolipoprotein B Gene 3' Hypervariable Region Among Nationals of the Abu Dhabi Emirate and Comparisons with Other Populations. Annals of Saudi Medicine. 19(6). 490–494. 4 indexed citations
10.
Frossard, Philippe M., Emmanuelle Girodon, K. P. Dawson, et al.. (1998). Identification of cystic fibrosis mutations in the United Arab Emirates. Human Mutation. 11(5). 412–413. 39 indexed citations
11.
Frossard, Philippe M., et al.. (1998). The Angiotensin-Converting Enzyme (ACE) Gene Insertion/Deletion Dimorphism Tracks with Higher Serum ACE Activities in Both Younger and Older Subjects. Annals of Saudi Medicine. 18(5). 389–392. 4 indexed citations
12.
Lestringant, G.G., Virginia P. Sybert, Moshe Frydman, et al.. (1997). Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde. The American Journal of Human Genetics. 61(1). 94–100. 51 indexed citations
13.
Frossard, Philippe M. & Gilles G. Lestringant. (1995). Association between a dimorphic site on chromosome 12 and clinical diagnosis of hypertension in three independent populations. Clinical Genetics. 48(6). 284–287. 14 indexed citations
14.
Ijaz, M. Khalid, Marta Sabara, P.J. Frenchick, et al.. (1995). Characterization of a synthetic peptide mimicking trypsin-cleavage site of rotavirus VP4. Comparative Immunology Microbiology and Infectious Diseases. 18(3). 145–160. 2 indexed citations
15.
Frossard, Philippe M., et al.. (1994). TaqI dimorphic site in a human pancreatic phospholipase A2 (PLA2) gene localized on chromosome 12. Human Genetics. 93(6). 720–720. 2 indexed citations
16.
Faraco, Juliette, Nigel A. Morrison, Andrew J. Baker, John Shine, & Philippe M. Frossard. (1989). ApaI dimorphism at the human vitamin D receptor gene locus. Nucleic Acids Research. 17(5). 2150–2150. 93 indexed citations
17.
Genest, Jacques, et al.. (1988). Two new ApoB gene polymorphisms: Rs1 and Rs2. Nucleic Acids Research. 16(17). 8746–8746. 1 indexed citations
18.
Masharani, Umesh, et al.. (1988). NsiI andScaI restriction fragment length polymorphisms at the atrial natriuretic peptides (ANP) gene locus. Human Genetics. 80(3). 307–307. 7 indexed citations
19.
Frossard, Philippe M., et al.. (1987). BanI dimorphic site in the third intron of the human apolipoprotein AI gene (Apo A1). Nucleic Acids Research. 15(1). 381–381. 1 indexed citations
20.
Frossard, Philippe M., et al.. (1986). Apal RFLP 5.4 kb 5′ to the human apolipoprotein AI (APO Al) gene. Nucleic Acids Research. 14(4). 1922–1922. 8 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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