John P Carulli

A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait.

Mark L. Johnson, P. van Eerdewegh, J. Carulli, 2002, American journal of human genetics.

A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica

Robert E Handsaker, Daniel G MacArthur, Karol Estrada, 2018, Nature Communications.

SMN deficiency in severe models of spinal muscular atrophy causes widespread intron retention and DNA damage

Norm Allaire, Adrian R Krainer, A. Krainer, 2017, Proceedings of the National Academy of Sciences.

Convergent Random Forest predictor: methodology for predicting drug response from genome-scale data applied to anti-TNF response.

Ronenn Roubenoff, Peter K Gregersen, P. Gregersen, 2009, Genomics.

STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus.

Wentian Li, Geoffrey Hom, Lars Alfredsson, 2007, The New England journal of medicine.

Application of functional genomic technologies in a mouse model of retinal degeneration.

Chunhua Yang, J. Carulli, J. Shearstone, 2005, Genomics.

CRIPTO3, a presumed pseudogene, is expressed in cancer.

Suzanne Szak, J. Carulli, M. Sanicola, 2008, Biochemical and biophysical research communications.

TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.

Anbupalam Thalamuthu, Wentian Li, David Altshuler, 2007, The New England journal of medicine.