J. Connolly

发表

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

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

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.

Michael J Ackerman, Joshua C Denny, Dan M Roden, 2016, JAMA.

Identification of Four Novel Loci in Asthma in European American and African American Populations

Peggy L. Peissig, Jennifer A. Pacheco, Iftikhar J. Kullo, 2017, American journal of respiratory and critical care medicine.

Quantifying the phenome‐wide disease burden of obesity using electronic health records and genomics

Jamie R. Robinson, Nephi A. Walton, Mayya S. Safarova, 2022, Obesity.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.

J. Glessner, H. Hakonarson, D. Roden, 2021, JAMA internal medicine.

Copy Number Variations in Alternative Splicing Gene Networks Impact Lifespan

Vilmundur Gudnason, Lenore J. Launer, Tamara B. Harris, 2013, PloS one.

Autism Spectrum Disorders : The Role of Genetics in Diagnosis and Treatment 52 2 . Heritability of ASDs

H. Hakonarson, J. Connolly, 2022 .

Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries

Joseph T. Glessner, J. Glessner, H. Qu, 2022, Biomedicines.

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.

Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples

J. Glessner, H. Qu, D. Slater, 2023, Genes.

Returning integrated genomic risk and clinical recommendations: the eMERGE study.

Melissa L. Habrat, Jorge A. Alsip, Kathleen F. Mittendorf, 2023, Genetics in medicine : official journal of the American College of Medical Genetics.

Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts

H. Hakonarson, J. Bradfield, F. Mentch, 2014, Front. Genet..

Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders

Joseph T. Glessner, J. Glessner, H. Hakonarson, 2023, Journal of Neurodevelopmental Disorders.

The Circassians and the Chechens in Jordan: results of a decade of epidemiological and genetic studies.

J. Glessner, H. Hakonarson, K. Shishani, 2023, Journal of community genetics.

Multiancestral polygenic risk score for pediatric asthma.

Theresa L. Walunas, Lisa J. Martin, H. Hakonarson, 2022, The Journal of allergy and clinical immunology.