
Arjun Bhattacharya
Department of Epidemiology, Division of Cancer Prevention and Population Sciences
Present Title & Affiliation
Primary Appointment
Assistant Professor, Department of Epidemiology, Division of Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, Texas
Affiliate, Department of Institute for Data Science in Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
Dual/Joint/Adjunct Appointment
Affiliate, Department of Institute for Data Science in Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas
Assistant Professor, Department of Epidemiology, The University of Texas MD Anderson Cancer Center, Houston, Texas
Education & Training
Degree-Granting Education
2020 | University of North Carolina at Chapel Hill, Chapel Hill, NC, US, Biostatistics, PhD |
Postgraduate Training
2020-2023 | Postdoctoral Fellow, Computational Medicine, University of California, Los Angeles, Los Angeles, CA |
Experience & Service
Other Appointments/Responsibilities
Fellow, University of California, Los Angeles, Los Angeles, California, 2021 - 2023
Institutional Committee Activities
Member, Student Success & Well-Being Committee Meeting, 2024 - Present
Honors & Awards
2024 | UT Rising STARs Award |
2023 | UCLA Institute for Quantitative and Computational Biosciences (QCB) Collaboratory Service Award |
2022 | Epstein Postdoctoral Award Semifinalist, American Society of Human Genetics |
2022 | Most Outstanding Oral Presentation, Early Career Investigator Program, International Society for Psychiatric Genetics |
2022 | James V. Neel Award, International Genetic Epidemiology Society |
2021 | UCLA Bruins in Genomics Mentorship Award, UCLA Institute for Quantitative and Computational Biosciences |
2021 | O'Malley Alumni Award for Publication Excellence in Population Sciences, The Gillings School of Global Public Health, University of North Carolina at Chapel Hill |
2018 | Training Fellowship in Breast Cancer Disparities, Susan G. Komen |
2011 | Innovation Scholarship, Mackenzie Family Foundation |
Professional Memberships
American Association for Cancer Research
2023 - Present
International Genetic Epidemiology Society
2019 - Present
American Society for Human Genetics
2018 - Present
Selected Publications
Peer-Reviewed Articles
- Venkateswaran, V, Boulier, K, Ding, Y, Johnson, R, Bhattacharya, A, Pasaniuc, B. Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles. Translational psychiatry 14(1), 2024. e-Pub 2024. PMID: 38238290.
- Chang Y, Head ST, Harrison T, Yu Y, Huff CD, Pasaniuc B, Lindström S, Bhattacharya A. Isoform-level analyses of 6 cancers uncover extensive genetic risk mechanisms undetected at the gene-level. medRxiv. e-Pub 2024. PMID: 39574839.
- Hervoso, JL, Amoah, K, Dodson, J, Choudhury, M, Bhattacharya, A, Quinones-Valdez, G, Pasaniuc, B, Xiao, X. Splicing-specific transcriptome-wide association uncovers genetic mechanisms for schizophrenia. American journal of human genetics 111(8):1573-1587, 2024. e-Pub 2024. PMID: 38925119.
- Xia, Y, Xia, C, Jiang, Y, Chen, Y, Zhou, J, Dai, R, Han, C, Mao, Z, Liu, C, Chen, C, Akbarian, S, Abyzov, A, Ahituv, N, Arasappan, D, Armenteros, JA, Beliveau, BJ, Bendl, J, Berretta, S, Bharadwaj, RA, Bhattacharya, A, Bicks, L, Brennand, KJ, Capauto, D, Champagne, FA, Chatterjee, T, Chatzinakos, C, Chen, Y, Chen, HI, Cheng, Y, Cheng, L, Chess, A, Chien, JF, Chu, Z, Clarke, D, Clement, A, Collado-Torres, L, Cooper, GM, Crawford, G, Daskalakis, NP, Davila-Velderrain, J, Deep-Soboslay, A, Deng, C, DiPietro, CP, Dracheva, S, Drusinsky, S, Duan, Z, Duong, D, Dursun, C, Eagles, NJ, Wang, H. Transcriptomic sex differences in postmortem brain samples from patients with psychiatric disorders. Science translational medicine 16(749), 2024. e-Pub 2024. PMID: 38781321.
- Wen, C, Margolis, M, Dai, R, Zhang, P, Przytycki, PF, Vo, DD, Bhattacharya, A, Matoba, N, Tang, M, Jiao, C, Kim, M, Tsai, E, Hoh, C, Aygün, N, Walker, RL, Chatzinakos, C, Clarke, D, Pratt, HE, Peters, MA, Gerstein, M, Daskalakis, NP, Weng, Z, Jaffe, AE, Kleinman, JE, Hyde, TM, Weinberger, DR, Bray, NJ, Sěstan, N, Geschwind, DH, Roeder, K, Gusev, A, Pasaniuc, B, Stein, JL, Love, MI, Pollard, KS, Liu, C, Gandal, MJ. Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain. Science 384(6698), 2024. e-Pub 2024. PMID: 38781368.
- Yap, CX, Vo, DD, Heffel, MG, Bhattacharya, A, Wen, C, Yang, Y, Kemper, KE, Zeng, J, Zheng, Z, Zhu, Z, Hannon, E, Vellame, DS, Franklin, A, Caggiano, C, Wamsley, B, Geschwind, DH, Zaitlen, N, Gusev, A, Pasaniuc, B, Mill, J, Luo, C, Gandal, MJ. Brain cell-type shifts in Alzheimer's disease, autism, and schizophrenia interrogated using methylomics and genetics. Science Advances 10(21), 2024. e-Pub 2024. PMID: 38781333.
- Shin, DS, Basak, S, Veena, MS, Comin-Anduix, B, Bhattacharya, A, Dong, TS, Ko, A, Han, P, Jacobs, J, Moatamed, N, Avila, L, Pellegrini, M, Wang, MB, Srivatsan, ES. Enhanced CTLA-4 blockade anti-tumor immunity with APG-157 combination in a murine head and neck cancer. Cancer medicine 13(9), 2024. e-Pub 2024. PMID: 38686626.
- Lo Faro, V, Bhattacharya, A, Zhou, W, Zhou, D, Wang, Y, Läll, K, Kanai, M, Lopera-Maya, EA, Straub, P, Pawar, P, Tao, R, Zhong, X, Namba, S, Sanna, S, Nolte, Im, Okada, Y, Ingold, N, MacGregor, S, Snieder, H, Surakka, I, Shortt, J, Gignoux, C, Rafaels, N, Crooks, K, Verma, A, Verma, SS, Guare, LA, Rader, DJ, Willer, CJ, Martin, AR, Brantley, MA, Gamazon, ER, Jansonius, NM, Joos, K, Cox, NJ, Hirbo, JB. Novel ancestry-specific primary open-angle glaucoma loci and shared biology with vascular mechanisms and cell proliferation. Cell Reports Medicine 5(2), 2024. e-Pub 2024. PMID: 38382466.
- Levey, DF, Galimberti, M, Deak, JD, Wendt, FR, Bhattacharya, A, Koller, D, Harrington, KM, Quaden, R, Johnson, EC, Gupta, P, Biradar, M, Lam, M, Cooke, M, Rajagopal, VM, Empke, SL, Zhou, H, Nunez, YZ, Kranzler, HR, Edenberg, HJ, Agrawal, A, Smoller, J, Lencz, T, Hougaard, DM, Børglum, AD, Demontis, D, Gaziano, JM, Gandal, MJ, Polimanti, R, Stein, MB, Gelernter, J. Multi-ancestry genome-wide association study of cannabis use disorder yields insight into disease biology and public health implications. Nature Genetics 55(12):2094-2103, 2023. e-Pub 2023. PMID: 37985822.
- Bhattacharya, A, Vo, DD, Jops, C, Kim, M, Wen, C, Hervoso, JL, Pasaniuc, B, Gandal, MJ. Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain. Nature Genetics 55(12):2117-2128, 2023. e-Pub 2023. PMID: 38036788.
- Petter, E, Ding, Y, Hou, K, Bhattacharya, A, Gusev, A, Zaitlen, N, Pasaniuc, B. Genotype error due to low-coverage sequencing induces uncertainty in polygenic scoring. American journal of human genetics 110(8):1319-1329, 2023. e-Pub 2023. PMID: 37490908.
- Mester, R, Hou, K, Ding, Y, Meeks, G, Burch, KS, Bhattacharya, A, Henn, B, Pasaniuc, B. Impact of cross-ancestry genetic architecture on GWASs in admixed populations. American journal of human genetics 110(6):927-939, 2023. e-Pub 2023. PMID: 37224807.
- Wang, X, Lu, Z, Bhattacharya, A, Pasaniuc, B, Mancuso, N. twas_sim, a Python-based tool for simulation and power analysis of transcriptome-wide association analysis. Bioinformatics 39(5), 2023. e-Pub 2023. PMID: 37099718.
- Hou, K, Ding, Y, Xu, Z, Wu, Y, Bhattacharya, A, Mester, R, Belbin, G, Buyske, S, Conti, DV, Darst, BF, Fornage, M, Gignoux, C, Guo, X, Haiman, CA, Kenny, EE, Kim, M, Kooperberg, C, Lange, L, Manichaikul, AW, North, KE, Peters, U, Rasmussen-Torvik, LJ, Rich, SS, Rotter, JI, Wheeler, HE, Wojcik, GL, Zhou, Y, Sankararaman, S, Pasaniuc, B. Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals. Nature Genetics 55(4):549-558, 2023. e-Pub 2023. PMID: 36941441.
- Johnson, R, Ding, Y, Bhattacharya, A, Knyazev, S, Chiu, A, Lajonchere, C, Geschwind, DH, Pasaniuc, B. The UCLA ATLAS Community Health Initiative. Cell Genomics 3(1), 2023. e-Pub 2023. PMID: 36777178.
- Wang, Y, Namba, S, Lopera, E, Kerminen, S, Tsuo, K, Läll, K, Kanai, M, Zhou, W, Wu, KH, Favé, MJ, Bhatta, L, Awadalla, P, Brumpton, B, Deelen, P, Hveem, K, Lo Faro, V, Mägi, R, Murakami, Y, Sanna, S, Smoller, J, Uzunovic, J, Wolford, BN, Wu, KH, Rasheed, H, Hirbo, JB, Bhattacharya, A, Zhao, H, Surakka, I, Lopera-Maya, EA, Chapman, SB, Karjalainen, J, Kurki, M, Mutaamba, M, Partanen, JJ, Chavan, S, Chen, TT, Daya, M, Ding, Y, Feng, YA, Gignoux, C, Graham, SE, Hornsby, WE, Ingold, N, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, IY, Palta, P, Pandit, A. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts. Cell Genomics 3(1), 2023. e-Pub 2023. PMID: 36777179.
- Kanai, M, Elzur, R, Zhou, W, Wu, KH, Rasheed, H, Tsuo, K, Hirbo, JB, Wang, Y, Bhattacharya, A, Zhao, H, Namba, S, Surakka, I, Wolford, BN, Lo Faro, V, Lopera-Maya, EA, Läll, K, Favé, MJ, Partanen, JJ, Chapman, SB, Karjalainen, J, Kurki, M, Maasha, M, Brumpton, B, Chavan, S, Chen, TT, Daya, M, Ding, Y, Feng, YA, Guare, LA, Gignoux, C, Graham, SE, Hornsby, WE, Ingold, N, Ismail, SI, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, IY, Moreno-Grau, S, Nam, K, Palta, P, Pandit, A, Preuss, M, Saad, C, Setia-Verma, S, Thorsteinsdottir, U, Uzunovic, J, Verma, A, Zawistowski, M. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution. Cell Genomics 2(12), 2022. e-Pub 2022. PMID: 36643910.
- Liu, W, Sun, Q, Huang, L, Bhattacharya, A, Wang, GW, Tan, X, Kuban, KC, Joseph, RM, O’Shea, TM, Fry, RC, Li, Y, Santos, HP. Innovative computational approaches shed light on genetic mechanisms underlying cognitive impairment among children born extremely preterm. Journal of neurodevelopmental disorders 14(1), 2022. e-Pub 2022. PMID: 35240980.
- Johnson, R, Ding, Y, Venkateswaran, V, Bhattacharya, A, Boulier, K, Chiu, A, Knyazev, S, Schwarz, T, Freund, M, Zhan, L, Burch, KS, Caggiano, C, Hill, B, Rakocz, N, Balliu, B, Denny, CT, Sul, JH, Zaitlen, N, Arboleda, VA, Halperin, E, Sankararaman, S, Butte, MJ, Lajonchere, C, Geschwind, DH, Pasaniuc, B. Leveraging genomic diversity for discovery in an electronic health record linked biobank. Genome medicine 14(1), 2022. e-Pub 2022. PMID: 36085083.
- Bhattacharya, A, Freedman, AN, Avula, V, Harris, R, Liu, W, Pan, C, Lusis, AJ, Joseph, RM, Smeester, L, Hartwell, HJ, Kuban, KC, Marsit, CJ, Li, Y, O’Shea, TM, Fry, RC, Santos, HP. Placental genomics mediates genetic associations with complex health traits and disease. Nature communications 13(1), 2022. e-Pub 2022. PMID: 35121757.
- Gandal, MJ, Haney, JR, Wamsley, B, Yap, CX, Parhami, S, Emani, PS, Chang, N, Chen, GT, Hoftman, GD, de Alba, D, Ramaswami, G, Hartl, C, Bhattacharya, A, Luo, C, Jin, T, Wang, D, Kawaguchi, R, Quintero, D, Ou, J, Wu, YE, Parikshak, NN, Swarup, V, Belgard, TG, Gerstein, MB, Pasaniuc, B, Geschwind, DH. Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD. Nature 611(7936):532-539, 2022. e-Pub 2022. PMID: 36323788.
- Zhao, H, Rasheed, H, Nøst, TH, Cho, Y, Liu, Y, Bhatta, L, Bhattacharya, A, Hemani, G, Davey Smith, G, Brumpton, B, Zhou, W, Neale, BM, Gaunt, TR, Zheng, J. Proteome-wide Mendelian randomization in global biobank meta-analysis reveals multi-ancestry drug targets for common diseases. Cell Genomics 2(11), 2022. e-Pub 2022. PMID: 36388766.
- Tsuo K, Zhou W, Kanai M, Wang Y, Namba S, Gupta R, Majara L, Nkambule LL, Morisaki T, Okada Y, Bhattacharya A, Neale BM, Meta-analysis Initiative GB, Daly MJ, Martin AR. Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Cell Genomics, 2022. e-Pub 2022. PMID: 36778051.
- Bhattacharya, A, Hirbo, JB, Zhou, D, Zhou, W, Zheng, J, Kanai, M, Pasaniuc, B, Gamazon, ER, Cox, NJ. Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies. Cell Genomics 2(10), 2022. e-Pub 2022. PMID: 36341024.
- Zhou, W, Kanai, M, Wu, KH, Rasheed, H, Tsuo, K, Hirbo, JB, Wang, Y, Bhattacharya, A, Zhao, H, Namba, S, Surakka, I, Wolford, BN, Lo Faro, V, Lopera-Maya, EA, Läll, K, Favé, MJ, Partanen, JJ, Chapman, SB, Karjalainen, J, Kurki, M, Maasha, M, Brumpton, B, Chavan, S, Chen, TT, Daya, M, Ding, Y, Feng, YA, Guare, LA, Gignoux, C, Graham, SE, Hornsby, WE, Ingold, N, Ismail, SI, Johnson, R, Laisk, T, Lin, K, Lv, J, Millwood, IY, Moreno-Grau, S, Nam, K, Palta, P, Pandit, A, Preuss, M, Saad, C, Setia-Verma, S, Thorsteinsdottir, U, Uzunovic, J, Verma, A, Zawistowski, M, Zhong, X. Global Biobank Meta-analysis Initiative. Cell Genomics 2(10), 2022. e-Pub 2022. PMID: 36777996.
- Partanen JJ, Häppölä P, Zhou W, Lehisto AA, Ainola M, Sutinen E, Allen RJ, Stockwell AD, Leavy OC, Bhattacharya A, Oldham JM, Guillen-Guio B, Cox NJ, Hirbo JB, Schwartz DA, Fingerlin TE, Flores C, Noth I, Yaspan BL, Jenkins R, Wain LV, Ripatti S, Pirinen M, Genetics Consortium II, Meta-Analysis Initiative GB, Laitinen T, Kaarteenaho R, Myllärniemi M, Daly MJ, Koskela JT. Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics. Cell Genomics, 2022. e-Pub 2022. PMID: 36777997.
- Jones, G, Hoadley, KA, Benefield, H, Olsson, LT, Hamilton, AM, Bhattacharya, A, Kirk, EL, Tipaldos, HJ, Fleming, JM, Williams, KP, Love, MI, Nichols, HB, Olshan, AF, Troester, MA. Racial differences in breast cancer outcomes by hepatocyte growth factor pathway expression. Breast Cancer Research and Treatment 192(2):447-455, 2022. e-Pub 2022. PMID: 35034243.
- Jones, G, Hoadley, KA, Olsson, LT, Hamilton, AM, Bhattacharya, A, Kirk, EL, Tipaldos, HJ, Fleming, JM, Love, MI, Nichols, HB, Olshan, AF, Troester, MA. Hepatocyte growth factor pathway expression in breast cancer by race and subtype. Breast Cancer Research 23(1), 2021. e-Pub 2021. PMID: 34344422.
- Bhattacharya, A, Hamilton, AM, Troester, MA, Love, MI. DeCompress. Nucleic acids research 49(8):E48, 2021. e-Pub 2021. PMID: 33524140.
- Bhattacharya, A, Hamilton, AM, Furberg, H, Pietzak, E, Purdue, MP, Troester, MA, Hoadley, KA, Love, MI. An approach for normalization and quality control for NanoString RNA expression data. Briefings in bioinformatics 22(3), 2021. e-Pub 2021. PMID: 32789507.
- Bhattacharya, A, Li, Y, Love, MI. MOSTWAS: Multi-Omic Strategies for Transcriptome-Wide Association Studies. PLoS genetics 17(3), 2021. e-Pub 2021. PMID: 33684137.
- Santos, HP, Adynski, H, Harris, R, Bhattacharya, A, Incollingo Rodriguez, AC, Cali, R, Yabar, AT, Nephew, BC, Murgatroyd, C. Biopsychosocial correlates of psychological distress in Latina mothers. Journal of Affective Disorders 282:617-626, 2021. e-Pub 2021. PMID: 33445084.
- Patel, A, Garcia-Closas, M, Olshan, AF, Perou, CM, Troester, MA, Love, MI, Bhattacharya, A. Gene-Level Germline Contributions to Clinical Risk of Recurrence Scores in Black and White Patients with Breast Cancer. Cancer Research 82(1):25-35, 2021. e-Pub 2021. PMID: 34711612.
- Santos Jr HP, Bhattacharya A, Joseph RM, Smeester L, K Kuban KC, Marsit CJ, O'Shea T, Fry RC. Evidence for the placenta-brain axis: multi-omic kernel aggregation predicts intellectual and social impairment in children born extremely preterm. Molecular Autism, 2020. e-Pub 2020. PMID: 33308293.
- Bhattacharya A, García-Closas M, Olshan AF, Perou CM, Troester MA, Love MI. A framework for transcriptome-wide association studies in breast cancer in diverse study populations. Genome Biology, 2020. e-Pub 2020. PMID: 32079541.
- Santos Jr HP, Bhattacharya A, Martin EM, Addo K, Psioda M, Smeester L, Joseph RM, Hooper SR, Frazier JA, Kuban KC, O'Shea T, Fry RC. Epigenome-wide DNA methylation in placentas from preterm infants: association with maternal socioeconomic status. Epigenetics, 2019. e-Pub 2019. PMID: 31062658.
- Santos Jr HP, Nephew BC, Bhattacharya A, Tan X, Smith L, S Alyamani RA, Martin EM, Perreira K, Fry RC, Murgatroyd C. Discrimination exposure and DNA methylation of stress-related genes in Latina mothers. Psychoneuroendocrinology, 2018. e-Pub 2018. PMID: 30144780.
Other Articles
- Hou, K, Bhattacharya, A, Mester, R, Burch, KS, Pasaniuc, B On powerful GWAS in admixed populations. Nature Genetics 53(12):1631-1633, 2021. PMID: 34824480.
Selected Presentations & Talks
Local Presentations
- 2024. Considerations for computational molecular precision medicine. Invited. Houston, Texas, US.
- 2024. Considerations for computational molecular precision medicine. Invited. Grand Rounds. Houston, Texas, US.
Regional Presentations
- 2024. Integrative computational methods to unlock the wealth of information in bulk RNA-sequencing. Invited. Human Genetics Center Seminar Series. Houston, Texas, US.
National Presentations
- 2025. From wicked problems to incisive solutions: Fast-tracking innovative pediatric interventions and policy in an era of complexity. Panelist. Pediatric Academic Societies Annual Meeting 2025. Honolulu, Hawaii, US.
- 2024. Inferring gene isoform mechanisms underlying genetic associations with cancer risk. Invited. UNC Biostatistics 75th Anniversary Celebration. Chapel Hill, North Carolina, US.
- 2024. Isoform-specific analyses to uncover hidden cancer risk mechanisms. Invited. Division of Epidemiology Seminar Series. Nashville, Tennessee, US.
- 2024. Integrative computational methods to unlock the wealth of information in bulk RNA-sequencing. Conference. STATGEN 2024. Pittsburgh, Pennsylvania, US.
- 2024. Integrative computational methods to unlock the wealth of information in bulk RNA-sequencing. Invited. UNC-Chapel Hill Biostatistics Genomics Seminar. Chapel Hill, North Carolina, US.
- 2023. Isoform-level transcriptome-wide association studies uncover novel biological mechanisms underlying genetic associations with neuropsychiatric traits. Invited. The American College of Neuropharmocology Annual Meeting. Tampa, Florida, US.
- 2023. Gene-level germline associations with breast cancer subtype and survival. Invited. Breast Ovarian Consortia Meeting, US.
- 2023. Isoform-level transcriptome-wide association studies uncover novel biological mechanisms underlying genetic associations with neuropsychiatric traits. Invited. University of Pennsylvania Symposium on Genetics and Epigenetics of Behavior. Philadelphia, Pennsylvania, US.
International Presentations
- 2025. Isoform-specific analyses to uncover hidden cancer risk mechanisms. Invited. 1.Novel Statistical Approaches for Studying Multi-omics Data Workshop. Banff, CA.
Grant & Contract Support
Date: | 2025 - 2029 |
Title: | Multi-ancestry study of mammographic density |
Funding Source: | NCI |
Role: | Co-I |
ID: | R01CA298162 |
Date: | 2025 - 2030 |
Title: | Understanding the contribution of placental genomics to gestational diabetes-associated childhood metabolic outcome disparities with a novel multi-ancestry transcriptomic reference |
Funding Source: | NIH: NICHD |
Role: | PI |
ID: | FP00024022 |
Date: | 2025 - 2027 |
Title: | A unified software suite to integrate genetic variation, isoform quantifications, and phenotypic associations to understand complex disease etiology |
Funding Source: | NCI |
Role: | PI |
ID: | FP00024567 |
Date: | 2025 - 2028 |
Title: | The effects of burn pit and toxicant exposure to lung cancer risk and progression via alternative splicing and transcript-isoform expression moderation |
Funding Source: | DOD |
Role: | PI |
ID: | FP00024659 |
Date: | 2025 - 2030 |
Title: | Understanding the contribution of placental genomics to gestational diabetes-associated childhood metabolic outcome disparities with a novel multi-ancestry transcriptomic reference |
Funding Source: | NIH |
Role: | PI |
Date: | 2024 - 2029 |
Title: | Multi-ancestry study of mammographic density |
Funding Source: | NCI |
Role: | Co-I |
ID: | FP00022415 |
Date: | 2024 - 2026 |
Title: | Alternative splicing and isoform expression as mediators for the genetic etiology of breast cancer |
Funding Source: | NIH |
Role: | PI |
ID: | FP00020740 |
CV information above last modified March 03, 2025