Varaico: Literature-Extracted Genetic Variants

Gene:GDF15
Variant:p.H202D
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GDF15

NM_004864.4:p.H202D

Associated Papers

Multi-ancestry GWAS of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity.

Fejzo M et al.

Research Square, 2024

HAPLN3 p.T34A contributes to incomplete penetrance of moyamoya disease in Chinese carrying RNF213 p.R4810K.

Xu J et al.

European Journal of Neurology, 2024

39315749 (PubMed )
Supplement: ENE-31-e16473-s001.xlsx › Table_S2

Multi-ancestry GWAS of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity.

Fejzo M et al.

Medrxiv : the Preprint Server for Health Sciences, 2024

Identification and characterization of human GDF15 knockouts.

Gurtan AM et al.

Nature Metabolism, 2024

Total and H-specific GDF-15 levels increase in caloric deprivation independently of leptin in humans.

Chrysafi P et al.

Nature Communications, 2024

GDF15 linked to maternal risk of nausea and vomiting during pregnancy.

Fejzo M et al.

Nature, 2024

Fetally-encoded GDF15 and maternal GDF15 sensitivity are major determinants of nausea and vomiting in human pregnancy.

Fejzo M et al.

Biorxiv : the Preprint Server for Biology, 2023

The Common H202D Variant in GDF-15 Does Not Affect Its Bioactivity but Can Significantly Interfere with Measurement of Its Circulating Levels.

Karusheva Y et al.

The Journal of Applied Laboratory Medicine, 2022

Genomic characterization of lymphomas in patients with inborn errors of immunity.

Ye X et al.

Blood Advances, 2022

35687490 (PubMed )
Supplement: advancesADV2021006654-suppl4.xlsx › PL23

Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans.

Lemmelä S et al.

Elife, 2022

Synergistic insights into human health from aptamer- and antibody-based proteomic profiling.

Pietzner M et al.

Nature Communications, 2021

34819519 (PubMed )
Supplement: 41467_2021_27164_MOESM2_ESM.pdf

Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.

Li Y et al.

Molecular Medicine Reports, 2020

32705272 (PubMed )
Supplement: Supplementary_Data1.xlsx › filter_by_duplicate

Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.

Fejzo MS et al.

Nature Communications, 2018

Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Karageorgos I et al.

Human Genomics, 2015

26092435 (PubMed )
Supplement: 40246_2015_34_MOESM1_ESM.xlsx › FamilyB

H6D polymorphism in macrophage-inhibitory cytokine-1 gene associated with prostate cancer.

Lindmark F et al.

Journal of the National Cancer Institute, 2004

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."