H. Guillermit

490 total citations
10 papers, 353 citations indexed

About

H. Guillermit is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, H. Guillermit has authored 10 papers receiving a total of 353 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pulmonary and Respiratory Medicine, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in H. Guillermit's work include Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (4 papers) and Congenital Ear and Nasal Anomalies (3 papers). H. Guillermit is often cited by papers focused on Cystic Fibrosis Research Advances (9 papers), Neonatal Respiratory Health Research (4 papers) and Congenital Ear and Nasal Anomalies (3 papers). H. Guillermit collaborates with scholars based in France, Switzerland and Germany. H. Guillermit's co-authors include Claude Férec, Bernard Mercier, I. Quéré, C. Verlingue, M.‐P. Audrézet, Marie‐Pierre Audrézet, G. Rault, Ulrich Wulbrand, Thomas Neumann and Julian Zielenski and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Human Molecular Genetics.

In The Last Decade

H. Guillermit

10 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
H. Guillermit France	8	308	98	42	29	20	10	353
Ling Jun Huan Canada	7	194 0.6×	15 0.2×	101 2.4×	21 0.7×	22 1.1×	8	261
Anya T. Joynt United States	8	247 0.8×	31 0.3×	108 2.6×	53 1.8×	8 0.4×	11	317
Javier Sanz Switzerland	7	158 0.5×	29 0.3×	83 2.0×	29 1.0×	5 0.3×	16	263
Melis A. Aksit United States	8	171 0.6×	26 0.3×	84 2.0×	40 1.4×	16 0.8×	17	239
Carmelina Magnani Italy	7	136 0.4×	42 0.4×	38 0.9×	13 0.4×	5 0.3×	9	178
T. Piskáčková Czechia	6	65 0.2×	9 0.1×	28 0.7×	16 0.6×	5 0.3×	6	152
Lisa Wagner-Britz Germany	8	181 0.6×	58 0.6×	115 2.7×	8 0.3×	1 0.1×	8	349
Julie Goepp Canada	10	303 1.0×	10 0.1×	130 3.1×	16 0.6×	1 0.1×	12	390
Anne-Marie Van Der Kevie-Kersemaekers Netherlands	7	30 0.1×	11 0.1×	92 2.2×	124 4.3×	10 0.5×	13	212
Arianna Franca United States	6	79 0.3×	23 0.2×	73 1.7×	40 1.4×	4 0.2×	6	153

Countries citing papers authored by H. Guillermit

Since Specialization

Citations

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

Fields of papers citing papers by H. Guillermit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Guillermit. 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 H. Guillermit. The network helps show where H. Guillermit may publish in the future.

Co-authorship network of co-authors of H. Guillermit

This figure shows the co-authorship network connecting the top 25 collaborators of H. Guillermit. A scholar is included among the top collaborators of H. Guillermit 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 H. Guillermit. H. Guillermit 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:

10 of 10 papers shown

1.

Jehanne, M, M.‐P. Audrézet, Bernard Mercier, et al.. (1994). Association of 1078 del T cystic fibrosis mutation with severe disease.. Journal of Medical Genetics. 31(2). 159–161. 7 indexed citations

2.

Guillermit, H., et al.. (1993). A novel mutation in exon 3 of the CFTR gene. Human Genetics. 91(3). 233–5. 13 indexed citations

3.

Férec, Claude, C. Verlingue, Marie‐Pierre Audrézet, et al.. (1993). Prenatal Diagnosis of Cystic Fibrosis in Different European Populations: Application of Denaturing Gradient Gel Electrophoresis. Fetal Diagnosis and Therapy. 8(5). 341–350. 7 indexed citations

4.

Audrézet, Marie‐Pierre, Bernard Mercier, H. Guillermit, et al.. (1993). Identification of 12 novel mutations in the CFTR gene. Human Molecular Genetics. 2(1). 51–54. 60 indexed citations

5.

Dörk, Thilo, Thomas Neumann, Ulrich Wulbrand, et al.. (1992). Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families. Human Genetics. 88(4). 417–425. 58 indexed citations

6.

Férec, Claude, M.‐P. Audrézet, Bernard Mercier, et al.. (1992). Detection of over 98% cystic fibrosis mutations in a Celtic population. Nature Genetics. 1(3). 188–191. 139 indexed citations

7.

Quéré, I., H. Guillermit, Bernard Mercier, Marie‐Pierre Audrézet, & Claude Férec. (1991). A polymorphism in intron 20 of the CFTR gene. Nucleic Acids Research. 19(19). 5453–5453. 8 indexed citations

8.

Férec, Claude, H. Guillermit, & André Chaventré. (1991). [Gene mutations of cystic fibrosis in Brittany population].. PubMed. 39(6). 577–80. 3 indexed citations

9.

Vidaud, Michel, Claude Férec, Olivier Attree, et al.. (1990). Frequency of the cystic fibrosis ΔF508 mutation in a large sample of the French population. Human Genetics. 85(4). 434–435. 6 indexed citations

10.

Guillermit, H., et al.. (1990). A 3′ splice site consensus sequence mutation in the cystic fibrosis gene. Human Genetics. 85(4). 450–453. 52 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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