List of works - Cuiping Hou

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

scientific article

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

scientific article published on 10 September 2008

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

scientific article

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

scientific article

Common genetic variants on 5p14.1 associate with autism spectrum disorders

scientific article

Common variants at five new loci associated with early-onset inflammatory bowel disease

scientific article

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

scientific article published on 18 September 2017

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

scientific article

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

scientific article

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

scientific article

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy

scientific article published on 17 July 2015

Copy number variation at 1q21.1 associated with neuroblastoma

scientific article

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

scientific article

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

scientific article

Examination of genetic variants influencing lipid traits in pediatric populations.

scientific article

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

scientific article published on 10 July 2009

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

scientific article

Genome-wide association identifies diverse causes of common variable immunodeficiency

scientific article published on 17 April 2011

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.

scientific article

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

scientific article

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.

scientific article published on 13 January 2009

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.

scientific article published in March 2009

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

scientific article

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

scientific article

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

scientific article

Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa

scientific article published on 29 January 2019

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.

scientific article published on 23 March 2016

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

scholarly article by Dong Li published in June 2018

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

scientific article published on 14 January 2020

Strong synaptic transmission impact by copy number variations in schizophrenia

scientific article

The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.

scientific article published on January 2013

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

scientific article

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

scientific article

Variants of DENND1B associated with asthma in children

scientific article

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

scientific article

Whole-genome sequencing in an autism multiplex family

scientific article (publication date: 18 April 2013)

List of works by Cuiping Hou

A genome-wide study reveals copy number variants exclusive to childhood obesity cases

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Common variants at five new loci associated with early-onset inflammatory bowel disease

Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies

Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food Allergy

Copy number variation at 1q21.1 associated with neuroblastoma

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

Examination of genetic variants influencing lipid traits in pediatric populations.

Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes.

Genome-wide association identifies diverse causes of common variable immunodeficiency

Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.

Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964).

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations

Strong synaptic transmission impact by copy number variations in schizophrenia

The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.

The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature

Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility

Variants of DENND1B associated with asthma in children

Whole-genome DNA/RNA sequencing identifies truncating mutations in RBCK1 in a novel Mendelian disease with neuromuscular and cardiac involvement

Whole-genome sequencing in an autism multiplex family