Nicolas Derive

412 citations
16 papers · 283 · 1 hit paper · h-index 6

Impact in

  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Neurological disorders and treatments

Papers in

    • Genomics and Rare Diseases 5
    • Genetics and Neurodevelopmental Disorders 4
    • BRCA gene mutations in cancer 3
    • Genetic and Kidney Cyst Diseases 1
    • Cancer and Skin Lesions 1

Nicolas Derive

13 papers receiving 279 citations

Nicolas Derive's Hit Papers

PFMG2025–integrating genomic medicine into the national healthcare system in France 2025 · 26 citations
260Years since publication510152025

Peers

Nicolas Derive
Comparison fields: 5 of 35
  • Genetics 198
  • Neurology 18
  • Cell Biology 17
  • Cancer Research 13
  • Reproductive Medicine 7
Replace KA Rauen with:
KA Rauen United States
M. Cecilia Cirio United States
Jonathan M. Downie United States
Pierre de Langen France
M Katoh Japan
Lara A. Underkoffler United States
Philip Smith United Kingdom
Luis Daniel Campos-Acevedo Mexico
Goranka Tanačković Switzerland
Setareh Moghadasi Netherlands
Nicolas Derive relative to KA Rauen United States KA Rauen's profile →
Citations per field
00.5×5×10.5×
KA Rauen · 1×
Citations per year

Countries citing papers authored by Nicolas Derive

Since Specialization
Citations

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

Fields of papers citing papers by Nicolas Derive

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Nicolas Derive, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nicolas Derive Line = papers co-authored together Nicolas Derive links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1 2019121
2 201651
3
PFMG2025–integrating genomic medicine into the national healthcare system in France
Hit paper breakdown →
202526
4 201524
5 202122
6 202118
7 20216
8 20244
9 20233
10 20243
11 20232
12 20232
13 20231
14 20240
15 20240
16 20240

About Nicolas Derive

Nicolas Derive is a scholar working on Genetics, Dermatology, Pediatrics, Perinatology and Child Health, Cell Biology and Neurology, having authored 16 papers that have together received 283 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), BRCA gene mutations in cancer (3 papers), Cancer and Skin Lesions (1 paper), Salivary Gland Tumors Diagnosis and Treatment (1 paper), Microtubule and mitosis dynamics (1 paper), Urinary and Genital Oncology Studies (1 paper) and Genetic and Kidney Cyst Diseases (1 paper). The work is most often cited by research in Genetics (198 citations), Neurology (18 citations), Cell Biology (17 citations), Cancer Research (13 citations) and Reproductive Medicine (7 citations). Nicolas Derive has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Anne Royou, Émilie Montembault, Derek McCusker, Damien Goutte-Gattat, Pierre Laurent‐Puig, Dries Dobbelaere, Guilhem Bousquet, Souhail Bennani, Lyse Ruaud and Cyril Gitiaux. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, European Journal of Human Genetics, The Journal of Cell Biology and JCO Precision Oncology.

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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