| 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 | 1706 | 2020 |
| 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 | 436 | 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 | 325 | 2021 |
| 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 | 233 | 2014 |
| Functional genomics of PCOS: from GWAS to molecular mechanisms JM McAllister, RS Legro, BP Modi, JF Strauss Trends in Endocrinology & Metabolism 26 (3), 118-124, 2015 | 217 | 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 | 157 | 2018 |
| The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies J Manry, P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, ... Proceedings of the National Academy of Sciences 119 (21), 2022 | 128 | 2022 |
| 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 | 57 | 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 | 42 | 2016 |
| 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 | 39 | 2019 |
| Inborn errors of immunity manifesting as atopic disorders M Vaseghi-Shanjani, KL Smith, RJ Sara, BP Modi, A Branch, M Sharma, ... Journal of Allergy and Clinical Immunology 148 (5), 1130-1139, 2021 | 29 | 2021 |
| 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 | 25 | 2017 |
| 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 | 20 | 2018 |
| Defects in Ovarian Steroid Hormone Biosynthesis JF Strauss III, B Modi, JM McAllister Cellular Endocrinology in Health and Disease, 285-309, 2014 | 17 | 2014 |
| 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 | 14 | 2020 |
| A second update on mapping the human genetic architecture of COVID-19 M Kanai, SJ Andrews, M Cordioli, C Stevens, BM Neale, M Daly, A Ganna, ... Nature 621 (7977), E7-E26, 2023 | 12 | 2023 |
| 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 | 12 | 2016 |
| 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 | 11 | 2017 |
| Adult GAMT deficiency: A literature review and report of two siblings BP Modi, HN Khan, R van der Lee, M Wasim, CA Haaxma, PA Richmond, ... Molecular Genetics and Metabolism Reports 27, 100761, 2021 | 10 | 2021 |
| Human complete NFAT1 deficiency causes a triad of joint contractures, osteochondromas, and B-cell malignancy M Sharma, MP Fu, HY Lu, AA Sharma, BP Modi, C Michalski, S Lin, ... Blood, The Journal of the American Society of Hematology 140 (17), 1858-1874, 2022 | 9 | 2022 |
Wyeth WassermanProfessor of Medical Genetics, University of British ColumbiaVerified email at cmmt.ubc.ca
