Utrecht University (UU)
Universiteit Utrecht (UU)

Netherlands

1 May 2019 - 30 April 2020

Region: Global
Subject/journal group: All

The table to the right includes counts of all research outputs for Utrecht University (UU) published between 1 May 2019 - 30 April 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
667 128.32

Outputs by subject (Share)

Subject Count Share
Physical Sciences 265 37.52
Earth & Environmental Sciences 139 36.63
Life Sciences 270 50.33
13 0.72
De Novo Variants in SPOP Cause Two Clinically Distinct Neurodevelopmental Disorders.
2020-02-25
0.09
Genome-Wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length.
2020-02-20
0.02
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
TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities.
2019-11-12
0.08
TRIDENT-2: National Implementation of Genome-Wide Non-Invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
2019-10-31
0.08
Heterozygous Variants in the Mechanosensitive Ion Channel TMEM63A Result in Transient Hypomyelination during Infancy.
2019-09-27
0.05
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital Arthrogryposis.
2019-08-28
0.02
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.
2019-08-16
0.03
Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy.
2019-08-07
0.06
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies.
2019-07-23
0.06
De Novo Heterozygous POLR2A Variants Cause a Neurodevelopmental Syndrome with Profound Infantile-Onset Hypotonia.
2019-07-20
0.14
De Novo Variants Disturbing the Transactivation Capacity of POU3F3 Cause a Characteristic Neurodevelopmental Disorder.
2019-07-02
0.08
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
2019-05-09
0.01
4 0.08
10 1.17
1 0.17
8 1.05
10 4.05
3 1.22
3 0.22
1 0.32
2 0.16
6 2.88
4 1.68
5 0.29
1 0.06
6 4.02
1 0.25
10 0.80
16 1.89
3 0.29
4 0.11
1 0.05
54 9.82
8 0.22
4 0.34
4 0.68
1 0.06
5 1.02
2 0.88
2 0.87
3 0.38
21 4.74
5 0.62
6 0.44
11 1.66
3 0.08
11 2.61
4 1.11
1 0.10
13 3.19
Chemistry 64 19.77

1 May 2019 - 30 April 2020

International vs. domestic collaboration by Share

  • 24.61% Domestic
  • 75.39% International

Note: Hover over the graph to view the percentage of collaboration.

Note: Collaboration is determined by the fractional count (Share), which is listed in parentheses.

Affiliated joint institutions and consortia

Return to institution outputs