Associated Papers
Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals.
Stanzick KJ et al.
Nature Communications, 2021
Impact of rare and common genetic variation in the interleukin-1 pathway on human cytokine responses.
van Deuren RC et al.
Genome Medicine, 2021
34034819 (PubMed )
Supplement: 13073_2021_907_MOESM1_ESM.xlsx › Table_S3
Genetic alterations in necrotizing enterocolitis.
Cuna A et al.
Seminars in Perinatology, 2017
SIGIRR genetic variants in premature infants with necrotizing enterocolitis.
Sampath V et al.
Pediatrics, 2015
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases.
Maciąg A et al.
Bmc Genetics, 2015
25888430 (PubMed )
Supplement: 12863_2015_177_MOESM1_ESM.xls › Sheet1
SIGIRR gene variants in term newborns with congenital heart defects and necrotizing enterocolitis.
Zaikova EK et al.
Annals of Pediatric Cardiology, 0
Observation on SIGIRR gene variants in term newborns with congenital heart defects and necrotizing enterocolitis.
Siham MA
Annals of Pediatric Cardiology, 0
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