France

1 June 2019 - 31 May 2020

Subject/journal group: All

The table to the right includes counts of all research outputs for France published between 1 June 2019 - 31 May 2020 which are tracked by the Nature Index.

Hover over the donut graph to view the FC output for each subject. Below, the same research outputs are grouped by subject. Click on the subject to drill-down into a list of articles organized by journal, and then by title.

Note: Articles may be assigned to more than one subject area.

Count Share
5067 2273.68

Outputs by subject (FC)

Subject Count Share
Earth & Environmental Sciences 852 338.24
Physical Sciences 1747 721.25
Life Sciences 1693 699.67
34 7.94
A Genetic History of the Near East from an aDNA Time Course Sampling Eight Points in the Past 4,000 Years.
2020-05-25
0.08
Bi-allelic Variations of SMO in Humans Cause a Broad Spectrum of Developmental Anomalies Due to Abnormal Hedgehog Signaling.
2020-05-12
0.56
Analysis of U8 snoRNA Variants in Zebrafish Reveals How Bi-allelic Variants Cause Leukoencephalopathy with Calcifications and Cysts.
2020-05-07
0.13
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy.
2020-04-28
0.36
Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy
2020-03-26
0.11
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.
2020-03-16
0.03
De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.
2020-03-11
0.64
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification.
2020-03-05
0.05
Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders.
2020-02-26
0.46
Opposite Modulation of RAC1 by Mutations in TRIO Is Associated with Distinct, Domain-Specific Neurodevelopmental Disorders.
2020-02-25
0.52
Genome-Wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.
2020-02-20
0.05
Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
2020-01-23
0.03
TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella.
2020-01-22
1
Bi-allelic Variants in TKFC Encoding Triokinase/FMN Cyclase Are Associated with Cataracts and Multisystem Disease.
2020-01-17
0.07
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency.
2020-01-03
0.13
Bi-Allelic UQCRFS1 Variants Are Associated with Mitochondrial Complex III Deficiency, Cardiomyopathy, and Alopecia Totalis.
2019-12-23
0.06
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism.
2019-12-23
0.15
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects.
2019-12-17
0.02
Gain-of-Function MN1 Truncation Variants Cause a Recognizable Syndrome with Craniofacial and Brain Abnormalities.
2019-12-12
0.04
Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction.
2019-11-25
0.16
Making the Most of Clumping and Thresholding for Polygenic Scores.
2019-11-15
0.63
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
2019-11-12
0.06
Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
2019-11-05
0.78
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals.
2019-10-21
0.05
RPL13 Variants Cause Spondyloepimetaphyseal Dysplasia with Severe Short Stature.
2019-10-14
0.76
De Novo Pathogenic Variants in N-cadherin Cause a Syndromic Neurodevelopmental Disorder with Corpus Collosum, Axon, Cardiac, Ocular, and Genital Defects.
2019-10-03
0.16
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype.
2019-10-03
0.05
Distinct HLA Associations with Rheumatoid Arthritis Subsets Defined by Serological Subphenotype.
2019-08-26
0.05
Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation.
2019-08-05
0.39
Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.
2019-08-01
0.05
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
2019-07-23
0.09
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia.
2019-07-20
0.09
Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.
2019-07-19
0.05
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.
2019-07-02
0.08
8 4.21
23 11.01
30 6.70
10 4.02
14 6.94
5 1.13
55 30.40
20 7.79
21 9.04
6 2.66
11 4.16
9 1.75
61 33.80
17 10.92
26 12.23
16 6.32
25 13.73
23 7.98
20 5.49
1 0.09
67 12.90
8 2.70
12 3.57
10 4.22
374 147.67
21 2.30
8 3.42
24 4.25
9 3.48
8 2.73
10 3.72
18 7.19
47 24.33
43 21.57
191 84.21
53 24.42
47 12.91
85 38.26
20 9.77
26 13.13
20 9.34
19 9.95
138 65.36
Chemistry 1324 717.02

1 June 2019 - 31 May 2020

View the connected world of international research collaboration. Visualize collaborations by subject or region.

Collaborations between countries

Percentage of collaboration by Share

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Top 10 collaborators by Share

  • France
  1. 424.79
    665.14
  2. Germany (624.34)
    285.09
    339.25
  3. 226.05
    286.38
  4. China (323)
    134.39
    188.61
  5. Italy (270.55)
    134.42
    136.13
  6. Switzerland (267.95)
    127.91
    140.04
  7. Spain (264.44)
    136.60
    127.84
  8. Japan (190.06)
    96.92
    93.15
  9. Canada (171.23)
    91.09
    80.14
  10. Netherlands (149.64)
    77.99
    71.66

Collaboration is determined by the combined fractional count (Share) of France and the collaborating country.

Top 10 institutions from France

Institution Count Share
1. French National Centre for Scientific Research (CNRS) 4452 740.19
2. Sorbonne University 1081 105.32
3. The French Alternative Energies and Atomic Energy Commission (CEA) 887 94.26
4. National Institute for Health and Medical Research (INSERM) 1009 86.50
5. University of Paris 779 76.03
6. University of Paris-Sud (UPSud) 669 69.52
7. University of Strasbourg 411 59.14
8. University of Toulouse 419 53.58
9. University of Lyon 410 49.50
10. Aix-Marseille University (AMU) 420 48.81

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