List of works - Patrick M Sleiman

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

scientific article

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

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 at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

scientific article

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

scientific article

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

scientific journal article

Variants of DENND1B associated with asthma in children

scientific article

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

scientific article

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

scientific article

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

scientific article

Neuroimaging of the Philadelphia neurodevelopmental cohort

scientific article

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

scientific journal article

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

scientific article

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

scientific article published on 19 October 2015

Strong synaptic transmission impact by copy number variations in schizophrenia

scientific article

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

scientific article

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

scientific article

The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth

scientific article

The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative

scientific article

The psychosis spectrum in a young U.S. community sample: findings from the Philadelphia Neurodevelopmental Cohort

scientific article

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

article by Matthew B. Lanktree et al published June 2012 in American Journal of Human Genetics

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

scientific article

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

scientific article

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

scientific article

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

scientific article

Meta-analysis identifies seven susceptibility loci involved in the atopic march

scientific article

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

scientific article

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

scientific article published on 10 July 2009

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

article

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

scientific article

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

scientific article (publication date: 29 October 2013)

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

scientific article

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

scientific article published on January 2013

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

scientific article

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

scientific article published on 18 September 2017

BMD-associated variation at the Osterix locus is correlated with childhood obesity in females

scientific article published on 06 January 2011

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

scientific article published on 01 July 2019

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

scientific article published on 17 July 2015

Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity.

scientific article published on 2 February 2016

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

scholarly article by Dong Li published in June 2018

Copy number variations in alternative splicing gene networks impact lifespan

scientific article

An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder

scientific article published on 7 March 2016

Detecting multiple differentially methylated CpG sites and regions related to dimensional psychopathology in youths

scientific article published on 21 October 2019

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

scientific article published on 29 January 2019

Corrigendum: An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder

scientific article published on 24 May 2016

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

scientific article

Examination of genetic variants influencing lipid traits in pediatric populations.

scientific article

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

scientific article published on 14 January 2020

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network

List of works by Patrick M Sleiman

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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

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 at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

Common variants at 5q22 associate with pediatric eosinophilic esophagitis

Variants of DENND1B associated with asthma in children

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

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

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

Neuroimaging of the Philadelphia neurodevelopmental cohort

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

Strong synaptic transmission impact by copy number variations in schizophrenia

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

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth

The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative

The psychosis spectrum in a young U.S. community sample: findings from the Philadelphia Neurodevelopmental Cohort

ERRATUM: Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

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

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

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

Meta-analysis identifies seven susceptibility loci involved in the atopic march

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

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

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

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

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

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

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

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

BMD-associated variation at the Osterix locus is correlated with childhood obesity in females

ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitor

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

Genome-wide investigation of schizophrenia associated plasma Ndel1 enzyme activity.

Pathogenic variant in EPHB4 results in central conducting lymphatic anomaly

Copy number variations in alternative splicing gene networks impact lifespan

An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder

Detecting multiple differentially methylated CpG sites and regions related to dimensional psychopathology in youths

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

Corrigendum: An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder

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

Examination of genetic variants influencing lipid traits in pediatric populations.

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

Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network