France

1 December 2019 - 30 November 2020

Subject/journal group: All

The table to the right includes counts of all research outputs for France published between 1 December 2019 - 30 November 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
4999 2196.20

Outputs by subject (FC)

Subject Count Share
Earth & Environmental Sciences 802 320.55
Life Sciences 1728 715.26
36 6.92
Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome.
2020-11-05
0.10
NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism.
2020-11-05
0.10
Plasma DNA Profile Associated with DNASE1L3 Gene Mutations: Clinical Observations, Relationships to Nuclease Substrate Preference, and In Vivo Correction.
2020-11-05
0.04
RLIM Is a Candidate Dosage-Sensitive Gene for Individuals with Varying Duplications of Xq13, Intellectual Disability, and Distinct Facial Features.
2020-10-28
0.19
Global Public Perceptions of Genomic Data Sharing: What Shapes the Willingness to Donate DNA and Health Data?
2020-09-14
0.02
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
2020-08-31
0.01
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia.
2020-08-06
0.02
De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects.
2020-08-06
0.09
High Levels of Genetic Diversity within Nilo-Saharan Populations: Implications for Human Adaptation.
2020-08-06
0.06
Mutations in MYLPF Cause a Novel Segmental Amyoplasia that Manifests as Distal Arthrogryposis.
2020-08-06
0.16
Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk
2020-07-29
0.03
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling
2020-07-04
0.15
The Genetic Landscape and Epidemiology of Phenylketonuria.
2020-07-01
0.04
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.
2020-06-24
0.34
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay.
2020-06-12
0.15
De Novo SOX6 Variants Cause a Neurodevelopmental Syndrome Associated with ADHD, Craniosynostosis, and Osteochondromas.
2020-06-04
0.28
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement.
2020-06-04
0.70
Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy.
2020-06-04
0.36
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
0.07
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
6 1.55
30 13.92
29 5.81
7 2.45
16 6.94
4 1.10
64 33.91
18 6.18
16 8.56
4 0.83
14 6.38
17 4.70
60 31.93
24 14.82
35 15.27
18 7.45
30 16.75
17 7.19
25 6.53
1 0.09
77 14.23
7 1.77
17 7.37
6 2.51
375 160.21
13 1.81
10 2.49
24 3.77
9 1.88
8 2.96
7 2.76
22 6.22
32 14.12
42 23.12
176 74.35
47 21.92
54 17.96
99 40.64
16 6.69
29 16.05
22 11.98
14 6.85
151 74.29
Physical Sciences 1789 717.52
Chemistry 1249 648.20

1 December 2019 - 30 November 2020

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

Collaborations between countries

Percentage of collaboration by Share

Hover over the graph to view the percentage of collaboration.

Top 10 collaborators by Share

  • France
  1. 422.26
    656.65
  2. Germany (587.96)
    262.70
    325.26
  3. 229.04
    285.42
  4. China (335.01)
    133.26
    201.75
  5. Switzerland (288.16)
    138.79
    149.36
  6. Italy (282.02)
    137.55
    144.47
  7. Spain (239.47)
    125.49
    113.98
  8. Japan (204.91)
    104.80
    100.11
  9. Netherlands (158.85)
    81.14
    77.71
  10. Canada (156.94)
    76.78
    80.17

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) 4417 700.85
2. Sorbonne University 1070 98.02
3. National Institute for Health and Medical Research (INSERM) 1145 89.79
4. The French Alternative Energies and Atomic Energy Commission (CEA) 907 87.42
5. University of Paris 831 80.07
6. University of Paris-Sud (UPSud) 647 61.36
7. University of Strasbourg 392 51.77
8. Aix-Marseille University (AMU) 410 49.44
9. University of Toulouse 409 49.29
10. University of Lyon 446 48.72

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