Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis is a research paper published in American Journal of Medical Genetics Part A (2022). On theSindex it has a DataRank of 0. It has been cited 7 times.
Scored on demand from live citation data
Linked data & code
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National Institutes of Health
Grant: 1R03OD030597‐01
National Institutes of Health
Grant: 3UM1HG006348‐10S2
National Institutes of Health
Grant: K23HL136932
NIH HHS
Grant: R03 OD030597
NHGRI NIH HHS
Grant: UM1 HG006348
National Institutes of Health
Grant: 3UM1HG006348-10S2
KOMP2 Administrative Supplement-Using Mouse Essentiality Screen to Identify Disease Genes Causing Severe Human Phenotypes With Early Lethality
National Institutes of Health
Grant: 5K23HL136932-03
The Discovery of Novel Genes in Inherited Sudden Arrhythmic Death Syndromes
National Institutes of Health
Grant: 1R03OD030597-01
Expanding the List of Human Disease Genes Using the Knockout Mouse Phenotyping Program (KOMP2) Data to Reassess Human Clinical Data
FWCI
0.65
Citation Percentile
0.6%
Citation Trend
Fields of Study
MeSH Terms
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Sustainable Development Goals