Associated Papers
The trans-ancestral genomic architecture of glycemic traits.
Chen J et al.
Nature Genetics, 2021
34059833 (PubMed )
Supplement: EMS120610-supplement-Supplementary_Tables.xlsx › S14-88signalsPPAg0.9
Functional Validation of CLDN Variants Identified in a Neural Tube Defect Cohort Demonstrates Their Contribution to Neural Tube Defects.
Baumholtz AI et al.
Frontiers in Neuroscience, 2020
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
Fragoza R et al.
Nature Communications, 2019
31515488 (PubMed )
Supplement: 41467_2019_11959_MOESM11_ESM.xlsx › SD7_-_Drug_Targets
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › e__Freq_TP095
Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.
van Schouwenburg PA et al.
Clinical Immunology (orlando, Fla.), 2015
26122175 (PubMed )
Supplement: NIHMS64345-supplement-Supplementary_tables.xlsx › Table_S7
Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects.
De Marco P et al.
Journal of Molecular Neuroscience : Mn, 2013
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