Florence Fellmann

4.5k total citations
54 papers, 1.4k citations indexed

About

Florence Fellmann is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Florence Fellmann has authored 54 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 18 papers in Genetics and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Florence Fellmann's work include Cardiovascular Effects of Exercise (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Cardiac electrophysiology and arrhythmias (6 papers). Florence Fellmann is often cited by papers focused on Cardiovascular Effects of Exercise (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Cardiac electrophysiology and arrhythmias (6 papers). Florence Fellmann collaborates with scholars based in Switzerland, France and United Kingdom. Florence Fellmann's co-authors include Martina C. Cornel, Carla van El, Heidi Howard, Ros Hastings, Wybo Dondorp, Pascal Borry, Lisbeth Tranebjærg, Shirley V. Hodgson, Hans Scheffer and Hanne Meijers‐Heijboer and has published in prestigious journals such as Nature Communications, Neurology and Journal of Allergy and Clinical Immunology.

In The Last Decade

Florence Fellmann

48 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Fellmann Switzerland 18 691 417 227 193 188 54 1.4k
Lora Jh Bean United States 24 606 0.9× 862 2.1× 162 0.7× 176 0.9× 216 1.1× 58 1.6k
Boleslaw Goldman Israel 22 575 0.8× 746 1.8× 94 0.4× 179 0.9× 246 1.3× 74 1.7k
Dianne Abuelo United States 23 768 1.1× 757 1.8× 158 0.7× 80 0.4× 298 1.6× 52 1.9k
Christopher J. Groves United Kingdom 20 569 0.8× 459 1.1× 75 0.3× 99 0.5× 89 0.5× 33 1.3k
Ishwar C. Verma India 20 386 0.6× 625 1.5× 75 0.3× 69 0.4× 325 1.7× 139 1.7k
Gail V. Benson United States 13 457 0.7× 894 2.1× 292 1.3× 139 0.7× 71 0.4× 16 1.9k
Ayumi Takakura United States 17 726 1.1× 915 2.2× 233 1.0× 94 0.5× 51 0.3× 28 1.6k
Tanya N. Nelson Canada 21 450 0.7× 308 0.7× 126 0.6× 38 0.2× 276 1.5× 51 1.0k
Ralph Telgmann Germany 16 249 0.4× 315 0.8× 198 0.9× 72 0.4× 40 0.2× 30 1.2k
Katarina Trebušak Podkrajšek Slovenia 22 278 0.4× 373 0.9× 57 0.3× 89 0.5× 81 0.4× 92 1.2k

Countries citing papers authored by Florence Fellmann

Since Specialization
Citations

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

Fields of papers citing papers by Florence Fellmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Fellmann

This figure shows the co-authorship network connecting the top 25 collaborators of Florence Fellmann. A scholar is included among the top collaborators of Florence Fellmann 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 Florence Fellmann. Florence Fellmann 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.
Wert, Guido de, Carla van El, Angus Clarke, et al.. (2025). Cascade counselling and testing. Recommendations of the European Society of Human Genetics. European Journal of Human Genetics. 34(2). 171–184.
2.
Fellmann, Florence, Jan Nový, Sébastien Lebon, et al.. (2024). Tuberous sclerosis: a survey in the canton of Vaud, Switzerland. Frontiers in Medicine. 11. 1513619–1513619.
3.
Haro, Endika, Florence Petit, Fabienne Escande, et al.. (2021). Identification of limb-specific Lmx1b auto-regulatory modules with Nail-patella syndrome pathogenicity. Nature Communications. 12(1). 5533–5533. 15 indexed citations
4.
Bibert, Stéphanie, Jocelyne Piret, Mathieu Quinodoz, et al.. (2019). Herpes simplex encephalitis in adult patients with MASP-2 deficiency. PLoS Pathogens. 15(12). e1008168–e1008168. 19 indexed citations
5.
Phan-Hug, Franziska, Ariane Paoloni‐Giacobino, Florence Fellmann, et al.. (2016). [Patients with variations of sex development : an example of interdisciplinary care].. PubMed. 12(538). 1923–1929. 1 indexed citations
6.
Phan-Hug, Franziska, Ariane Paoloni‐Giacobino, Florence Fellmann, et al.. (2016). Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaire. Revue Médicale Suisse. 12(538). 1923–1929. 2 indexed citations
7.
Wilhelm, Matthias, Stephan A. Bolliger, Christine Bärtsch, et al.. (2015). Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach. Swiss Medical Weekly. 145(2526). w14129–w14129. 31 indexed citations
8.
Fernández‐Vizarra, Erika, Malik Alawi, K. Gerhard Brand, et al.. (2015). Mutations in NDUFB11, Encoding a Complex I Component of the Mitochondrial Respiratory Chain, Cause Microphthalmia with Linear Skin Defects Syndrome. The American Journal of Human Genetics. 96(4). 640–650. 60 indexed citations
9.
El, Carla van, Martina C. Cornel, Pascal Borry, et al.. (2013). Whole-genome sequencing in health care. European Journal of Human Genetics. 21(6). 580–584. 256 indexed citations
10.
Chehade, Hassib, François Cachat, Éric Girardin, et al.. (2013). Two new families with hereditary minimal change disease. BMC Nephrology. 14(1). 65–65. 4 indexed citations
11.
Spring, Philipp, et al.. (2013). Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis. American Journal of Dermatopathology. 35(2). 241–245. 7 indexed citations
12.
Bochud, Murielle, Florence Fellmann, & Idris Guessous. (2012). Les tests génétiques peuvent-ils être utiles pour la prévention cardiovasculaire ?. Archive ouverte UNIGE (University of Geneva). 1 indexed citations
13.
Grilo, Liliana Sintra, Jürg Schläpfer, Florence Fellmann, & Hugues Abriel. (2011). Patient with Syncope and LQTS Carrying a Mutation in the PAS Domain of the hERG1 Channel. Annals of Noninvasive Electrocardiology. 16(2). 213–218. 1 indexed citations
14.
Cristofaro, Julie Di, Catherine Metzler‐Guillemain, Nicolas Lévy, et al.. (2011). HSFY genes and the P4 palindrome in the AZFb interval of the human Y chromosome are not required for spermatocyte maturation. Human Reproduction. 27(2). 615–624. 25 indexed citations
15.
Beckmann, J., et al.. (2010). [R74W;R1070W;D1270N]: A new complex allele responsible for cystic fibrosis. Journal of Cystic Fibrosis. 9(6). 447–449. 6 indexed citations
16.
Michaud, Katarzyna, Florence Fellmann, Hugues Abriel, et al.. (2009). Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration. SERVAL (Université de Lausanne). 8 indexed citations
17.
Ferrarini, Alberto, Maria‐Chiara Osterheld, Yvan Vial, et al.. (2009). Familial occurrence of an association of multiple intestinal atresia and choanal atresia: A new syndrome?. American Journal of Medical Genetics Part A. 149A(12). 2661–2665.
18.
Michaud, Katarzyna, et al.. (2008). [b]L’autopsie[/b] moléculaire de la mort subite cardiaque : de la salle d’autopsie au cabinet du praticien. Revue Médicale Suisse. 4(164). 1590–1593. 1 indexed citations
19.
Aknin‐Seifer, Isabelle, Renaud Touraine, Anne-Karen Faure, et al.. (2005). Two fast methods for detection of Y-microdeletions. Fertility and Sterility. 84(3). 740–742. 9 indexed citations
20.
Roux, Claude, et al.. (2005). Segregation of chromosomes in sperm of Robertsonian translocation carriers. Cytogenetic and Genome Research. 111(3-4). 291–296. 61 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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