Outputs for Edward Mallinckrodt Department of Pediatrics, WUSTL

1 August 2019 - 31 July 2020

United States of America (USA)

Country: United States Of America (USA)

Sector: Healthcare

Subject/journal group: All

Count Share
24 2.85

The research outputs below are grouped by journal. Click on the journal to view the list of articles.

Journal Count Share
American Journal of Human Genetics 5 0.18
Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum.
2020-07-20
0.02
Delineation of a Human Mendelian Disorder of the DNA Demethylation Machinery: TET3 Deficiency.
2020-01-03
0.06
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations.
2019-12-16
0.03
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
2019-10-11
0.03
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
2019-08-13
0.03
Journal of Clinical Investigation 1 0.05
Nature Communications 6 0.35
Neuron 1 0.01
PLOS Genetics 1 0.14
Proceedings of the National Academy of Sciences of the United States of America 7 0.96
Science 2 0.16
Science Advances 1 1

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