Laboratoire de Génétique Médicale

8.4k citations
313 papers ·

Impact in

    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
    • Genetic and Kidney Cyst Diseases
    • Genetic Syndromes and Imprinting
    • Mitochondrial Function and Pathology
    • Circular RNAs in diseases

Papers in

    • Genomic variations and chromosomal abnormalities 44
    • Genetics and Neurodevelopmental Disorders 32
    • Genetic Syndromes and Imprinting 17
    • Genetic and Kidney Cyst Diseases 15
    • Genomics and Rare Diseases 14

Laboratoire de Génétique Médicale

274 papers receiving 7.4k citations

Peers

Laboratoire de Génétique Médicale
Comparison fields: 5 of 163
  • Genetics 2.6k
  • Molecular Biology 4.1k
  • Cancer Research 674
  • Genetics 440
  • Sensory Systems 182
Replace Praxis für Humangenetik Tübingen with:
Praxis für Humangenetik Tübingen Germany
Medigene (Germany) Germany
Biologie du Développement et Cellules Souches France
Society of Paediatric Oncology and Haematology Germany
Altonaer Kinderkrankenhaus Germany
Hertie Foundation Germany
CeGaT (Germany) Germany
Institute of Clinical Cancer Research Germany
Adaptation Biologique et Vieillissement France
Diabetesinstitut Heidelberg Germany
Laboratoire de Génétique Médicale relative to Praxis für Humangenetik Tübingen Germany Praxis für Humangenetik Tübingen's profile →
Citations per field
00.5×1.5×2.0×
Praxis für Humangenetik Tübingen · 1×
Citations per year

Countries citing scholars working at Laboratoire de Génétique Médicale

Since Specialization
Citations

This map shows the geographic impact of research produced by authors working at Laboratoire de Génétique Médicale. 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 papers produced at Laboratoire de Génétique Médicale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laboratoire de Génétique Médicale more than expected).

Fields of papers published by authors at Laboratoire de Génétique Médicale

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers affiliated with Laboratoire de Génétique Médicale at the time of their publication. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers affiliated with Laboratoire de Génétique Médicale at the time of their publication.

About Laboratoire de Génétique Médicale

In recent decades, authors affiliated with Laboratoire de Génétique Médicale have published 313 papers, which have received a total of 8.4k indexed citations . Scholars at this organization have produced 114 papers in Genetics, 9 papers in Developmental Biology, 28 papers in Genetics, 139 papers in Molecular Biology and 34 papers in Pediatrics, Perinatology and Child Health on the topics of Genomic variations and chromosomal abnormalities (44 papers), Genetics and Neurodevelopmental Disorders (32 papers), Prenatal Screening and Diagnostics (27 papers), Genetic Syndromes and Imprinting (17 papers), Genetic and Kidney Cyst Diseases (15 papers), RNA modifications and cancer (15 papers), DNA Repair Mechanisms (14 papers) and Genomics and Rare Diseases (14 papers). Their work is cited by papers focused on Genetics (2.6k citations), Molecular Biology (4.1k citations), Cancer Research (674 citations), Genetics (440 citations) and Sensory Systems (182 citations). Authors at Laboratoire de Génétique Médicale collaborate with scholars in France, China and United States and have published in prestigious journals including European Journal of Medical Genetics, Clinical Genetics, Journal of Medical Genetics, European Journal of Human Genetics and Cytogenetic and Genome Research. Some of Laboratoire de Génétique Médicale's most productive authors include Claude Stoll, Marie‐Paule Roth, Yves Alembik, Béatrice Dott, Wei Li, Ping Yu, Huanyu Xu, Sen Guo, Arnold R. Kaplan and Edward V. Glanville.

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.

Explore institutions with similar magnitude of impact