Search Results - "Modi, Bhavi P."

Combined Long‐Read Genome and Transcriptome Sequencing Establishes Novel Variants in MEGF8 as the Cause for Carpenter Syndrome Type 2.

Authors: Rashidi, Kiana Modi, Bhavi P. Richmond, Phillip A. et al.

Source: American Journal of Medical Genetics. Part A; Jul2026, Vol. 200 Issue 7, p1719-1724, 6p

Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy.

Authors: Modi, Bhavi P. Del Bel, Kate L. Lin, Susan et al.

Source: Allergy, Asthma & Clinical Immunology. 1/14/2021, Vol. 17 Issue 1, p1-6. 6p.

Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes ( PPROM).

Authors: Modi, Bhavi P. Teves, Maria E. Pearson, Laurel N. et al.

Source: Molecular Genetics & Genomic Medicine. Nov2017, Vol. 5 Issue 6, p720-729. 10p.

3D genome evolution and reorganization in the Drosophila melanogaster species group.

Authors: Torosin, Nicole S. Anand, Aparna Golla, Tirupathi Rao et al.

Source: PLoS Genetics. 12/7/2020, Vol. 16 Issue 12, p1-29. 29p.

Human DENND1A.V2 Drives Cyp17a1 Expression and Androgen Production in Mouse Ovaries and Adrenals.

Authors: Teves, Maria E. Modi, Bhavi P. Kulkarni, Rewa et al.

Source: International Journal of Molecular Sciences. Apr2020, Vol. 21 Issue 7, p2545. 1p. 2 Diagrams, 8 Graphs.

Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth.

Authors: Modi, Bhavi P. Parikh, Hardik I. Teves, Maria E. et al.

Source: BMC Medical Genetics. 10/5/2018, Vol. 19 Issue 1, pN.PAG-N.PAG. 1p.

Abstracts.

Source: Journal of inherited metabolic disease Aug2024 Supplement 1; Vol. 47.

Journal Info: Publisher: Wiley-Blackwell ISSN: 0141-8955