List of works - Gabe Haller

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

scientific article published in Nature Communications

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis

scientific article

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

scientific article published on 01 May 2020

Are copy number variants associated with adolescent idiopathic scoliosis?

scientific article

Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis

scientific article published on 25 February 2019

Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis

scientific article

Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior

scientific article

Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells

scientific article

Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.

scientific article

Genome-wide association study identifies new disease loci for isolated clubfoot.

scientific article published on 25 March 2014

Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis

scientific article

Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine

scientific article

Positive Selection on Loci Associated with Drug and Alcohol Dependence

scientific article

Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence

scientific article published on 20 September 2013

Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.

scientific article published on 31 October 2011

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

scientific article (publication date: 2012)

Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis

scientific article (publication date: October 2014)

Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors

scientific article published on January 2010

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility

scientific article published on December 2009

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy

scientific article published on 28 March 2014

Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations

scientific article published on 01 January 2022

List of works by Gabe Haller

A missense variant in SLC39A8 is associated with severe idiopathic scoliosis

A polygenic burden of rare variants across extracellular matrix genes among individuals with adolescent idiopathic scoliosis

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Are copy number variants associated with adolescent idiopathic scoliosis?

Distal chromosome 16p11.2 duplications containing SH2B1 in patients with scoliosis

Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis

Functional characterization improves associations between rare non-synonymous variants in CHRNB4 and smoking behavior

Functional links between Drosophila Nipped-B and cohesin in somatic and meiotic cells

Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.

Genome-wide association study identifies new disease loci for isolated clubfoot.

Lack of joint hypermobility increases the risk of surgery in adolescent idiopathic scoliosis

Massively parallel single-nucleotide mutagenesis using reversibly terminated inosine

Positive Selection on Loci Associated with Drug and Alcohol Dependence

Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence

Rare missense variants in CHRNB4 are associated with reduced risk of nicotine dependence.

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis

Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy

Whole-exome analysis of adolescents with low VWF and heavy menstrual bleeding identifies novel genetic associations