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GWAS Study

Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.

Feenstra B, Geller F, Carstensen L et al.

23989729 PubMed ID
GWAS Study Type
7353 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FB
Feenstra B
GF
Geller F
CL
Carstensen L
RP
Romitti PA
KI
Körberg IB
BB
Bedell B
KC
Krogh C
FR
Fan R
SA
Svenningsson A
CM
Caggana M
NA
Nordenskjöld A
MJ
Mills JL
MJ
Murray JC
MM
Melbye M
Chapter II

Abstract

Summary of the research findings

Importance: Infantile hypertrophic pyloric stenosis (IHPS) is a serious condition in which hypertrophy of the pyloric sphincter muscle layer leads to gastric outlet obstruction. Infantile hypertrophic pyloric stenosis shows strong familial aggregation and heritability, but knowledge about specific genetic risk variants is limited.

1,001 European ancestry cases, 2,371 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

7353
Total Participants
GWAS
Study Type
Yes
Replicated
925 European ancestry cases, 1,621 European ancestry controls, 738 cases, 697 controls
Replication Participants
European, Other
Ancestry
Sweden, Denmark, U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.