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A Genome-Wide Scan of Ashkenazi Jewish Crohn's Disease Suggests Novel Susceptibility Loci

Jennifer Mulle, Nir Giladi, Karen Marder, 2012, PLoS genetics.

Location-Specific Oral Microbiome Possesses Features Associated With CKD

G. Nadkarni, Jianzhong Hu, X. Bao, 2017, Kidney international reports.

CYP2C9, CYP2C19 and CYP2D6 allele frequencies in the Ashkenazi Jewish population.

R. Desnick, S. Scott, L. Edelmann, 2007, Pharmacogenomics.

Homozygous nonsense mutations in TWIST2 cause Setleis syndrome.

E. Olson, R. Desnick, J. Richardson, 2010, American journal of human genetics.

Evaluation of 22 genetic variants with Crohn's Disease risk in the Ashkenazi Jewish population: a case-control study

R. Desnick, L. Mayer, D. Present, 2011, BMC Medical Genetics.

A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012, Nature Genetics.

A genome wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP 2 and within BBS 9

Alexander F. Wilson, A. F. Wilson, J. Richtsmeier, 2012 .

Nonsyndromic Craniosynostosis: Novel Coding Variants

K. Hao, J. Richtsmeier, B. Reva, 2019, Pediatric Research.

A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome

Janice S. Lee, M. Leppert, F. Collins, 2017, Nature Communications.