Bhavi P. Modi
Bhavi P. Modi
Research Associate, University of British Columbia
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JASPAR 2020: update of the open-access database of transcription factor binding profiles
O Fornes, JA Castro-Mondragon, A Khan, R van der Lee, X Zhang, ...
Nucleic acids research 48 (D1), D87-D92, 2020
Overexpression of a DENND1A isoform produces a polycystic ovary syndrome theca phenotype
JM McAllister, B Modi, BA Miller, J Biegler, R Bruggeman, RS Legro, ...
Proceedings of the National Academy of Sciences 111 (15), E1519-E1527, 2014
Functional genomics of PCOS: from GWAS to molecular mechanisms
JM McAllister, RS Legro, BP Modi, JF Strauss III
Trends in Endocrinology & Metabolism 26 (3), 118-124, 2015
Spontaneous preterm birth: advances toward the discovery of genetic predisposition
JF Strauss III, R Romero, N Gomez-Lopez, H Haymond-Thornburg, ...
American journal of obstetrics and gynecology 218 (3), 294-314. e2, 2018
Mutations in fetal genes involved in innate immunity and host defense against microbes increase risk of preterm premature rupture of membranes (PPROM)
BP Modi, ME Teves, LN Pearson, HI Parikh, H Haymond‐Thornburg, ...
Molecular genetics & genomic medicine 5 (6), 720-729, 2017
Alternative splicing of DENND1A, a PCOS candidate gene, generates variant 2
MK Tee, M Speek, B Legeza, B Modi, ME Teves, JM McAllister, ...
Molecular and cellular endocrinology 434, 25-35, 2016
Rare mutations and potentially damaging missense variants in genes encoding fibrillar collagens and proteins involved in their production are candidates for risk for preterm …
BP Modi, ME Teves, LN Pearson, HI Parikh, P Chaemsaithong, NU Sheth, ...
PloS one 12 (3), e0174356, 2017
miRNA profiling reveals miRNA-130b-3p mediates DENND1A variant 2 expression and androgen biosynthesis
JM McAllister, AX Han, BP Modi, ME Teves, GR Mavodza, ZL Anderson, ...
Endocrinology 160 (8), 1964-1981, 2019
Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth
BP Modi, HI Parikh, ME Teves, R Kulkarni, J Liyu, R Romero, TP York, ...
BMC medical genetics 19 (1), 1-13, 2018
Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science Immunology 6 (62), eabl4340, 2021
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science Immunology 6 (62), eabl4348, 2021
Human DENND1A. V2 Drives Cyp17a1 Expression and Androgen Production in Mouse Ovaries and Adrenals
ME Teves, BP Modi, R Kulkarni, AX Han, JS Marks, MA Subler, J Windle, ...
International Journal of Molecular Sciences 21 (7), 2545, 2020
The role of variants regulating metformin transport and action in women with polycystic ovary syndrome
CT Pau, KI Cheang, BP Modi, T Kasippillai, CC Keefe, M Shulleeta, ...
Pharmacogenomics 17 (16), 1765-1773, 2016
Defects in Ovarian Steroid Hormone Biosynthesis
JF Strauss III, B Modi, JM McAllister
Cellular Endocrinology in Health and Disease, 285-309, 2014
The Genetics of Polycystic Ovary Syndrome: From Genome-Wide Association to Molecular Mechanisms
JF Strauss, BP Modi, JM McAllister
Reproductive Medicine for Clinical Practice, 25-33, 2018
Expression patterns of the chromosome 21 MicroRNA cluster (miR-99a, miR-125b and let-7c) in chorioamniotic membranes
BP Modi, S Washington, SW Walsh, C Jackson-Cook, KJ Archer, ...
Placenta 49, 1-9, 2017
GeneBreaker: Variant simulation to improve the diagnosis of Mendelian rare genetic diseases
PA Richmond, TV Av‐Shalom, O Fornes, B Modi, AM Elliott, ...
Human Mutation 42 (4), 346-358, 2021
Clinical IRAK4 deficiency caused by homozygosity for the novel IRAK4 (c. 1049delG, p. Gly350Glufs* 15) variant
A Jia, E James, HY Lu, M Sharma, BP Modi, CM Biggs, KJ Hildebrand, ...
Molecular Case Studies 6 (3), a005298, 2020
Genetic and epigenetic mechanisms of complex reproductive disorders
BP Modi
Virginia Commonwealth University, 2016
Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy
BP Modi, KL Del Bel, S Lin, M Sharma, PA Richmond, ...
Allergy, Asthma & Clinical Immunology 17 (1), 1-6, 2021
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