D. Abrams

发表

Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum Disorder

Finale Doshi-Velez, Pei Chen, Joseph Bochenek, 2016, PloS one.

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

Johan Van Limbergen, David C Wilson, David C. Wilson, 2009, Nature Genetics.

A Comparison of Patient Satisfaction with Telehealth and On-Site Consultations: A Pilot Study for Prenatal Genetic Counseling

D. Abrams, M. Geier, 2006, Journal of Genetic Counseling.

An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities

J. Glessner, H. Hakonarson, F. Mentch, 2022, Journal of neurodevelopmental disorders.

Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis

J. Glessner, H. Hakonarson, B. Lie, 2022, Arthritis & rheumatology.

COVID-19 in pediatrics: Genetic susceptibility

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2022, Frontiers in Genetics.

Integrative Genetics Analysis of Juvenile Idiopathic Arthritis Identifies Novel Loci

John J. Connolly, Joseph T. Glessner, Debra K. Shivers, 2020, medRxiv.

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

Constantin Polychronakos, Yiran Guo, Dong Li, 2016 .

Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism

H. Hakonarson, Cecilia Kim, R. Chiavacci, 2016, BMC Urology.

Elevated levels of the cytokine LIGHT in Crohn's disease

F. Mentch, P. Sleiman, D. Abrams, 2021, medRxiv.

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network.

Robert C. Green, Keith Marsolo, Casey Overby Taylor, 2019, American journal of human genetics.

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Hongzhe Li, Constantin Polychronakos, Yiran Guo, 2015, Nature Communications.

Prenatally diagnosed mosaic trisomy 17: a case report with two‐year follow‐up

D. Abrams, M. Geier, A. Augustyn, 2005, Prenatal diagnosis.

Prevalence of chronic granulomatous disease in pediatric patients diagnosed with Crohn's disease.

R. Baldassano, K. Sullivan, D. Abrams, 2008, Inflammatory bowel diseases.

Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.

H. Hakonarson, Cecilia Kim, R. Chiavacci, 2015, Human reproduction.

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

Joseph T. Glessner, Hakon Hakonarson, Ryan M. Smith, 2008, Nature Genetics.

Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

H. Hakonarson, Cecilia Kim, Yiran Guo, 2017, Scientific Reports.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.

Association of the T300A non-synonymous variant of the ATG16L1 gene with susceptibility to paediatric Crohn’s disease

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Gut.

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

Joseph T. Glessner, Bradley P. Coe, B. Coe, 2020, Nature Communications.

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

B. Coe, E. Eichler, J. Glessner, 2020, Nature Communications.

Phenotype specific association of the TGFBR3 locus with nonsyndromic cryptorchidism.

H. Hakonarson, Cecilia Kim, R. Chiavacci, 2015, The Journal of urology.

Association of variants of the interleukin-23 receptor gene with susceptibility to pediatric Crohn's disease.

Joseph T. Glessner, Ryan M. Smith, J. Glessner, 2007, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.

Drug‐resistant epilepsy classified by a phenotyping algorithm associates with NTRK2

H. Hakonarson, D. Dlugos, P. Sleiman, 2019, Acta neurologica Scandinavica.

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

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

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

J. Glessner, H. Hakonarson, Cecilia Kim, 2015, Nature Medicine.

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

John J. Connolly, J. Glessner, H. Hakonarson, 2015, Nature Medicine.

A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling

John J. Connolly, I. Ntalla, E. Zeggini, 2017, Scientific Reports.