Melissa A. Gilbert

A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1

N. Spinner, H. Hakonarson, M. Devoto, 2018, PLoS genetics.

Alagille Syndrome: A Focused Review on Clinical Features, Genetics, and Treatment

K. Loomes, Melissa A Gilbert, Taisa J Kohut, 2021, Seminars in Liver Disease.

Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results

I. Krantz, N. Spinner, L. Conlin, 2020, Genetics in Medicine.

Alagille Syndrome: Genetics and Functional Models

N. Spinner, Melissa A Gilbert, Melissa A. Gilbert, 2017, Current Pathobiology Reports.

Human Mutation

I. Krantz, N. Spinner, B. Krock, 2019 .

Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

I. Krantz, N. Spinner, D. Piccoli, 2020, American journal of medical genetics. Part A.

Compound heterozygous mutations in NEK8 in siblings with end‐stage renal disease with hepatic and cardiac anomalies

N. Spinner, K. Coleman, M. Devoto, 2016, American journal of medical genetics. Part A.

A Comparison of Children Born Preterm and Full-Term on the Autism Spectrum in a Prospective Community Sample

J. Barbaro, Melissa A Gilbert, M. Yaari, 2020, Frontiers in Neurology.