Laboratoire de Génétique Médicale
- Research works
- 102 ▼ 26% vs 2013–17
- Citations
- 2.6k 25.1 per fractional work
- Top-10% rate
- 17.0% record average 16.5%
- Open access
- 31% world 28%
Not ranked overall: Laboratoire de Génétique Médicale is under the volume floor below which an excellence rate is noise. Not ranked is not the same as ranked last.
Field profile
Location quotient across every field it publishes in: outside the ring is more than an institution of this size would be expected to publish, inside it is less.
Rings at 0.5×, 1× and 2×. Widest outward: Biochemistry, Genetics and Molecular Biology, 9.3×. Every wedge is a field page.
Which keywords describe research at Laboratoire de Génétique Médicale?
By fractional works in all years, weighted toward what it does more of than the world: Genetic Mutations, Prenatal Diagnosis, Neurodevelopmental Disorders, Genomic Rearrangements, Copy Number Variation, Structural Variation, Cell-Free DNA and Aneuploidy Screening.
- Parental Influence
- Small RNAs
- Mutation
- Clinical Genomics
- Tumorigenesis
- Limb Malformations
- Genetic Heterogeneity
- Cancer Progression
- Prognostic Factors
- Hedgehog Signaling
- Genetic Variants
- Fragile X Syndrome
- Dendritic Spines
- Gene Expression
- Oxidative Stress
- Aneuploidy Screening
- Structural Variation
- Genomic Rearrangements
- Cancer
- Epidemiology
- Genetic Mutations
- Prenatal Diagnosis
- Neurodevelopmental Disorders
- Copy Number Variation
- Cell-Free DNA
- Maternal Plasma DNA Sequencing
- Epigenetic Regulation
- Brain Development
- Stem Cells
- Rett Syndrome
- Mitochondrial Dysfunction
- DNA Methylation
- Neural Crest
- Development
- Pancreatic Cancer
- Polydactyly
- Wnt Signaling
- Congenital Anomalies
- Sequence Interpretation
- Genomic Imprinting
Size is fractional works in all years in the topics tagged with each word; colour is the word's share of this institution's work against its share of the world's. The 40 words are chosen for being large and distinctive. Each links to the topic it comes from most.
All 40 words, with their numbers
- Genetic Mutations9▲ 17×17 topics
- Epidemiology8▲ 2.0×35 topics
- Prenatal Diagnosis7▲ 38×5 topics
- Cancer6▲ 4.0×24 topics
- Neurodevelopmental Disorders6▲ 35×4 topics
- Genomic Rearrangements5▲ 181×2 topics
- Copy Number Variation5▲ 195×1 topic
- Structural Variation5▲ 195×1 topic
- Cell-Free DNA5▲ 51×2 topics
- Aneuploidy Screening4▲ 121×1 topic
- Maternal Plasma DNA Sequencing4▲ 121×1 topic
- Oxidative Stress4▲ 2.2×22 topics
- Epigenetic Regulation4▲ 18×4 topics
- Gene Expression4▲ 6.1×10 topics
- Brain Development4▲ 17×3 topics
- Dendritic Spines3▲ 20×2 topics
- Stem Cells3▲ 11×9 topics
- Fragile X Syndrome3▲ 101×1 topic
- Rett Syndrome3▲ 101×1 topic
- Genetic Variants3▲ 15×4 topics
- Mitochondrial Dysfunction3▲ 8.1×8 topics
- Hedgehog Signaling3▲ 76×2 topics
- DNA Methylation3▲ 24×3 topics
- Prognostic Factors3▲ 6.1×8 topics
- Neural Crest2▲ 48×2 topics
- Cancer Progression2▲ 9.9×6 topics
- Development2▲ 6.7×3 topics
- Genetic Heterogeneity2▲ 93×2 topics
- Pancreatic Cancer2▲ 18×3 topics
- Limb Malformations2▲ 225×1 topic
- Polydactyly2▲ 225×1 topic
- Tumorigenesis2▲ 37×3 topics
- Wnt Signaling2▲ 16×5 topics
- Clinical Genomics2▲ 77×1 topic
- Congenital Anomalies2▲ 24×3 topics
- Mutation2▲ 12×3 topics
- Sequence Interpretation2▲ 77×1 topic
- Small RNAs2▲ 22×2 topics
- Genomic Imprinting2▲ 90×1 topic
- Parental Influence2▲ 90×1 topic
Which research topics does Laboratoire de Génétique Médicale publish most on?
By volume in 2022–2025: Prenatal Screening and Diagnostics, Assisted Reproductive Technology and Twin Pregnancy, Genomic variations and chromosomal abnormalities and Genomics and Rare Diseases.
Area is fractional works; colour is the subfield each topic belongs to.
- 1 Prenatal Screening and Diagnostics Pediatrics, Perinatology and Child Health 1 works
- 2 Assisted Reproductive Technology and Twin Pregnancy Pediatrics, Perinatology and Child Health 1 works
- 3 Genomic variations and chromosomal abnormalities Genetics 1 works
- 4 Genomics and Rare Diseases Genetics 1 works
- 5 Genetic Syndromes and Imprinting Genetics 0 works
- 6 Sperm and Testicular Function Reproductive Medicine 0 works
- 7 Sexual Differentiation and Disorders Molecular Biology 0 works
- 8 Genetic and Kidney Cyst Diseases Genetics 0 works
- 9 Genetic Neurodegenerative Diseases Cellular and Molecular Neuroscience 0 works
- 10 Reproductive Biology and Fertility Public Health, Environmental and Occupational Health 0 works
How open and international is its research?
Against the world’s own shares — the tick on each track. Both are shares of its output, so they sit on one scale and can be read against each other as well as against the world.
World: 28% of research is openly available.
World: 19% is written across borders.
How has Laboratoire de Génétique Médicale's research output changed?
Output in 2018–2022 was 26% lower than in 2013–2017.
The same series as a ribbon — one cell per year, darker for more. The line above answers how much; this answers when.
Other research institutions in Strasbourg
- Université de Strasbourg
- Hôpitaux Universitaires de Strasbourg
- Hôpital Civil, Strasbourg
- Institut de Physique et Chimie des Matériaux de Strasbourg
- Hôpital d'Hautepierre
- Institut de Biologie Moléculaire et Cellulaire
- Institut de Virologie
- Institut Charles Sadron
Research measures only: rankings here say nothing about teaching, admissions or student experience. Comparable institutions and collaboration partners are in the interactive view on the map.