Abhinav Jain, PhD

Title(s)Postdoctoral Scholar, Neurological Surgery
SchoolSchool of Medicine
Address1450 Third Street, #422
San Francisco CA 94158
Phone415-353-7500
Emailabhinav.jain@ucsf.edu
ORCID ORCID Icon0000-0001-6017-5492 Additional info
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    Collapse Biography 
    Collapse Education and Training
    Institute of Genomics and Integrative Biology, New Delhi, IndiaPhD08/2021Bioinformatics and Immunology
    Mayo Clinic, Rochester, MN, USA07/2024Computational Immunology
    Collapse Awards and Honors
    Council of Scientific and Industrial Research2016  - 2021CSIR UGC National Eligibility Test
    Ministry of Human Resources Development2016  - 2021Graduate Aptitute Test in Engineering

    Collapse Overview 
    Collapse Overview
    I am a computational biologist Ph.D. in Bioinformatics and immunology. I have more than 8 years of extensive experience in analyzing single cell dataset (scRNA, scMultiome, scCITESeq, BEAM-T, Spatial, and scTCRseq), Cycif image, bulk (Genome, Exome, RNA, and ATAC), flow cytometry and microarray. Using single cell dataset I have developed supervised machine learning model to annotate the immune cell types. I have developed web based database using RShiny for bench scientist and developed pipeline using Nextflow.

    Currently I am post doctoral fellow in Dr. Aaron Diaz lab in UCSF and collaborator in Dr. Jorg Goronzy's lab in Mayo Clinic. My project in UCSF focused on SHH Medulloblastoma primary vs recurrent difference using snRNA, snATAC, and Visium. Another project focused on lineage tracing of Medullobastoma using mutable and static barcode. My project in Mayo Clinic is focused on understanding the immune aging using scCITEseq, scTCR, scMultiome, spatial, and flow cytometry dataset. I works closely in collaboration on multiple projects with wet-lab scientist which involved analyzing scRNA, spatial, BEAM-T, spatial, Cycif Image, bulk RNA, ATAC etc.

    During graduation I have worked on national consortium projects:
    1. I have worked on one of the largest primary immunodeficiency cohort (>300 patients) where I have analyzed whole exome and genome datasets.
    2. I was a part of a core bioinformatics team of IndiGen consortium, 1000 whole genome sequencing project for the Indian population.
    3. I was also part of the SARS-CoV-2 genome analysis bioinformatics core team and involved in the submission of over 1000 Indian isolates of SARS-CoV-2 genome in public repositories.

    Skills: Single cell and bulk data analysis, High Performance Computing, Machine Learning, Database development, AWS, R Shiny, R, Python, Bash/Shell scripting, Nextflow, Git.

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Haplotype analysis detects MLH1 founder variant in Indian Lynch syndrome patient cohort. Fam Cancer. 2024 Dec 19; 24(1):13. Sheth H, Sadhwani J, Jain A, Thenral SG, Ramprasad V, Bishop DT. PMID: 39702679.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Inappropriate use of proton pump inhibitors in clinical practice globally: a systematic review and meta-analysis. Gut. 2024 Dec 10; 74(1):e5. Dutta AK, Sharma V, Jain A, Elhence A, Panigrahi MK, Mohta S, Kirubakaran R, Philip M, Goenka M, Bhatia S, Dutta U, Reddy DN, Kochhar R, Makharia GK. PMID: 38670630.
      View in: PubMed   Mentions: 2     Fields:    
    3. Esophagitis dissecans superficialis - An intimidating, but innocuous condition. Indian J Gastroenterol. 2024 Dec; 43(6):1238-1239. Jain A, Patel R, Patel R. PMID: 37642936.
      View in: PubMed   Mentions:    Fields:    
    4. The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population-Scale Data. Mov Disord Clin Pract. 2024 Nov 13. Kumar M, Sharma S, Pandey S, Mammayil G, Pala Kuzhiyil A, Sreesh S, Arakkal R, Radhakrishnan DM, Rajan R, Amalnath D, Gulati R, Tayade N, Sadasivan S, Valsan A, Menon J, Kamate M, Mathur SK, Mahadevan R, Dhingra B, Rajan R, Singh K, Geevarghese SK, Kumar VS, Menachery J, Aliyar A, Bhoyar RC, Jolly B, Jain A, Vittal Rangan A, Moitra T, Mhaske A, Gupta V, Senthivel V, Mishra A, Saini A, Gaharwar U, Sivasubbu S, Scaria V, B K B. PMID: 39535360.
      View in: PubMed   Mentions:    Fields:    
    5. Aging trajectories of memory CD8 + T cells differ by their antigen specificity. bioRxiv. 2024 Jul 29. Sturmlechner I, Jain A, Hu B, Jadhav RR, Cao W, Okuyama H, Tian L, Weyand CM, Goronzy JJ. PMID: 39211225; PMCID: PMC11360919.
      View in: PubMed   Mentions:
    6. A sustainable bioprocess technology for producing food-flavour (+)-γ-decalactone from castor oil-derived ricinoleic acid using enzymatic activity of Candida parapsilosis: Scale-up optimization and purification using novel composite. J Biotechnol. 2024 Sep 20; 393:17-30. Syed N, Singh S, Chaturvedi S, Kumar P, Kumar D, Jain A, Sharma PK, Nannaware AD, Chanotiya CS, Bhambure R, Kumar P, Kalra A, Rout PK. PMID: 39025368.
      View in: PubMed   Mentions:    Fields:    Translation:Animals
    7. IKZF1 and UBR4 gene variants drive autoimmunity and Th2 polarization in IgG4-related disease. J Clin Invest. 2024 Jun 13; 134(16). Liu Q, Zheng Y, Sturmlechner I, Jain A, Own M, Yang Q, Zhang H, Pinto E Vairo F, Cerosaletti K, Buckner JH, Warrington KJ, Koster MJ, Weyand CM, Goronzy JJ. PMID: 38885295; PMCID: PMC11324302.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    8. Spectrum of rare and common mitochondrial DNA variations from 1029 whole genomes of self-declared healthy individuals from India. Comput Biol Chem. 2024 Oct; 112:108118. Gupta V, Jolly B, Bhoyar RC, Divakar MK, Jain A, Mishra A, Senthivel V, Imran M, Scaria V, Sivasubbu S. PMID: 38878606.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. Landscape of pharmacogenetic variants associated with non-insulin antidiabetic drugs in the Indian population. BMJ Open Diabetes Res Care. 2024 Mar 12; 12(2). Sivadas A, Sahana S, Jolly B, Bhoyar RC, Jain A, Sharma D, Imran M, Senthivel V, Divakar MK, Mishra A, Mukhopadhyay A, Gibson G, Narayan KV, Sivasubbu S, Scaria V, Kurpad AV. PMID: 38471670; PMCID: PMC10936492.
      View in: PubMed   Mentions: 1  Translation:Humans
    10. The genomic landscape of CYP2D6 variation in the Indian population. Pharmacogenomics. 2024 Feb; 25(3):147-160. Sivadas A, Rathore S, Sahana S, Jolly B, Bhoyar RC, Jain A, Sharma D, Imran M, Senthilvel V, Divakar MK, Mishra A, Sivasubbu S, Scaria V. PMID: 38426301.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    11. PREX1 improves homeostatic proliferation to maintain a naive CD4+ T cell compartment in older age. JCI Insight. 2024 Feb 08; 9(5). Zhang H, Okuyama H, Jain A, Jadhav RR, Wu B, Sturmlechner I, Morales J, Ohtsuki S, Weyand CM, Goronzy JJ. PMID: 38329813; PMCID: PMC10972599.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    12. Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality. Mitochondrion. 2024 Mar; 75:101844. Sabharwal A, Gupta V, Kv S, Kumar Manokaran R, Verma A, Mishra A, Bhoyar RC, Jain A, Sivadas A, Rawat S, Jolly B, Mohanty S, Gulati S, Gupta N, Kabra M, Scaria V, Sivasubbu S. PMID: 38237647.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    13. Investigation of RFC1 tandem nucleotide repeat locus in diverse neurodegenerative outcomes in an Indian cohort. Neurogenetics. 2024 Jan; 25(1):13-25. Tyagi N, Uppili B, Sharma P, Parveen S, Saifi S, Jain A, Sonakar A, Ahmed I, Sahni S, Shamim U, Anand A, Suroliya V, Asokachandran V, Srivastava A, Sivasubbu S, Scaria V, Faruq M. PMID: 37917284.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    14. Guidelines on optimizing the use of proton pump inhibitors: PPI stewardship. Indian J Gastroenterol. 2023 10; 42(5):601-628. Dutta AK, Jain A, Jearth V, Mahajan R, Panigrahi MK, Sharma V, Goenka MK, Kochhar R, Makharia G, Reddy DN, Kirubakaran R, Ahuja V, Berry N, Bhat N, Dutta U, Ghoshal UC, Jain A, Jalihal U, Jayanthi V, Kumar A, Nijhawan S, Poddar U, Ramesh GN, Singh SP, Zargar S, Bhatia S. PMID: 37698821.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    15. Stem-like CD4+ T cells in perivascular tertiary lymphoid structures sustain autoimmune vasculitis. Sci Transl Med. 2023 Sep 06; 15(712):eadh0380. Sato Y, Jain A, Ohtsuki S, Okuyama H, Sturmlechner I, Takashima Y, Le KC, Bois MC, Berry GJ, Warrington KJ, Goronzy JJ, Weyand CM. PMID: 37672564; PMCID: PMC11131576.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    16. Heterogeneity of memory T cells in aging. Front Immunol. 2023; 14:1250916. Jain A, Sturmlechner I, Weyand CM, Goronzy JJ. PMID: 37662959; PMCID: PMC10471982.
      View in: PubMed   Mentions: 5     Fields:    Translation:Cells
    17. T cell fate decisions during memory cell generation with aging. Semin Immunol. 2023 Sep; 69:101800. Sturmlechner I, Jain A, Mu Y, Weyand CM, Goronzy JJ. PMID: 37494738; PMCID: PMC10528238.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    18. Hepatocellular Carcinoma with Hepatic Vein and Inferior Vena Cava Invasion. J Clin Exp Hepatol. 2023 Sep-Oct; 13(5):813-819. Shukla A, Jain A. PMID: 37693266; PMCID: PMC10482991.
      View in: PubMed   Mentions: 1  
    19. Whole-genome sequencing of 1029 Indian individuals reveals unique and rare structural variants. J Hum Genet. 2023 Jun; 68(6):409-417. Divakar MK, Jain A, Bhoyar RC, Senthivel V, Jolly B, Imran M, Sharma D, Bajaj A, Gupta V, Scaria V, Sivasubbu S. PMID: 36813834.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    20. 1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variants. Hum Genomics. 2022 Aug 05; 16(1):30. Bajaj A, Senthivel V, Bhoyar R, Jain A, Imran M, Rophina M, Divakar MK, Jolly B, Verma A, Mishra A, Sharma D, Deepti S, Sharma G, Bansal R, Yadav R, Scaria V, Naik N, Sivasubbu S. PMID: 35932045; PMCID: PMC9354277.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    21. Landscape of Variability in Chemosensory Genes Associated With Dietary Preferences in Indian Population: Analysis of 1029 Indian Genomes. Front Genet. 2022; 13:878134. Prakrithi P, Jha P, Jaiswal J, Sharma D, Bhoyar RC, Jain A, Imran M, Senthilvel V, Divakar MK, Mishra A, Scaria V, Sivasubbu S, Mukerji M. PMID: 35903357; PMCID: PMC9315315.
      View in: PubMed   Mentions:
    22. Comprehensive Assessment of Indian Variations in the Druggable Kinome Landscape Highlights Distinct Insights at the Sequence, Structure and Pharmacogenomic Stratum. Front Pharmacol. 2022; 13:858345. Panda G, Mishra N, Sharma D, Kutum R, Bhoyar RC, Jain A, Imran M, Senthilvel V, Divakar MK, Mishra A, Garg P, Banerjee P, Sivasubbu S, Scaria V, Ray A. PMID: 35865963; PMCID: PMC9294532.
      View in: PubMed   Mentions:
    23. Hepatocellular Carcinoma Evaluation and Management for Physicians: Joint Gastroenterology Research Society and Association of Physicians of India Guidelines. J Assoc Physicians India. 2022 May; 70(5):11-12. Shukla A, Kale A, Gopan A, Jain A, Ramaswamy A, Phadke A, Sundaram A, Kantharia C, Darak H, Deshmukh H, Goel M, Doddmani M, Ingle M, Nadkar MY, Mehta N, Pai N, Shetty N, Parikh P, Buch P, Rathi P. PMID: 35598139.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    24. Pharmacogenomic landscape of Indian population using whole genomes. Clin Transl Sci. 2022 Apr; 15(4):866-877. Sahana S, Bhoyar RC, Sivadas A, Jain A, Imran M, Rophina M, Senthivel V, Kumar Diwakar M, Sharma D, Mishra A, Sivasubbu S, Scaria V. PMID: 35338580; PMCID: PMC9010271.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    25. Spatio-temporal dynamics of intra-host variability in SARS-CoV-2 genomes. Nucleic Acids Res. 2022 02 22; 50(3):1551-1561. Pathak AK, Mishra GP, Uppili B, Walia S, Fatihi S, Abbas T, Banu S, Ghosh A, Kanampalliwar A, Jha A, Fatma S, Aggarwal S, Dhar MS, Marwal R, Radhakrishnan VS, Ponnusamy K, Kabra S, Rakshit P, Bhoyar RC, Jain A, Divakar MK, Imran M, Faruq M, Sowpati DT, Thukral L, Raghav SK, Mukerji M. PMID: 35048970; PMCID: PMC8860616.
      View in: PubMed   Mentions: 13     Fields:    Translation:AnimalsCells
    26. An Alu insertion map of the Indian population: identification and analysis in 1021 genomes of the IndiGen project. NAR Genom Bioinform. 2022 Mar; 4(1):lqac009. Prakrithi P, Singhal K, Sharma D, Jain A, Bhoyar RC, Imran M, Senthilvel V, Divakar MK, Mishra A, Scaria V, Sivasubbu S, Mukerji M. PMID: 35178516; PMCID: PMC8846365.
      View in: PubMed   Mentions: 1  
    27. Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India. Hum Immunol. 2022 Apr; 83(4):335-345. Madathil Govindaraj G, Jain A, Edavazhippurath A, Bhoyar RC, Dhanasooraj D, Mishra A, Gupta V, Nair M, Shiny PM, Uppuluri R, Kumar A, Kashyap A, Ajith Kumar VT, Shankaran G, Senthivel V, Imran M, Kumar Divakar M, Sawant S, Dalvi A, Madkaikar M, Raj R, Sivasubbu S, Scaria V. PMID: 35074268.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    28. Genetic epidemiology of autoinflammatory disease variants in Indian population from 1029 whole genomes. J Genet Eng Biotechnol. 2021 Dec 14; 19(1):183. Jain A, Bhoyar RC, Pandhare K, Mishra A, Sharma D, Imran M, Senthivel V, Divakar MK, Rophina M, Jolly B, Batra A, Sharma S, Siwach S, Jadhao AG, Palande NV, Jha GN, Ashrafi N, Mishra PK, A K V, Jain S, Dash D, Kumar NS, Vanlallawma A, Sarma RJ, Chhakchhuak L, Kalyanaraman S, Mahadevan R, Kandasamy S, B M P, Rajagopal RE, Ramya J E, Devi P N, Bajaj A, Gupta V, Mathew S, Goswami S, Mangla M, Prakash S, Joshi K, S S, Gajjar D, Soraisham R, Yadav R, Devi YS, Gupta A, Mukerji M, Ramalingam S, B K B, Scaria V, Sivasubbu S. PMID: 34905135; PMCID: PMC8671593.
      View in: PubMed   Mentions:
    29. Variants of concern responsible for SARS-CoV-2 vaccine breakthrough infections from India. J Med Virol. 2022 Apr; 94(4):1696-1700. Singh UB, Rophina M, Chaudhry R, Senthivel V, Bala K, Bhoyar RC, Jolly B, Jamshed N, Imran M, Gupta R, Aggarwal P, Divakar MK, Sinha S, Arvinden VR, Bajaj A, Shamnath A, Jain A, COVID CBNAAT CORE GROUP, Scaria V, Sivasubbu S, Guleria R. PMID: 34786733; PMCID: PMC8662202.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCellsPHPublic Health
    30. Asymptomatic Reinfection in 2 Healthcare Workers From India With Genetically Distinct Severe Acute Respiratory Syndrome Coronavirus 2. Clin Infect Dis. 2021 11 02; 73(9):e2823-e2825. Gupta V, Bhoyar RC, Jain A, Srivastava S, Upadhayay R, Imran M, Jolly B, Divakar MK, Sharma D, Sehgal P, Ranjan G, Gupta R, Scaria V, Sivasubbu S. PMID: 32964927; PMCID: PMC7543380.
      View in: PubMed   Mentions: 113     Fields:    Translation:HumansCells
    31. Mammary-specific expression of Trim24 establishes a mouse model of human metaplastic breast cancer. Nat Commun. 2021 09 10; 12(1):5389. Shah VV, Duncan AD, Jiang S, Stratton SA, Allton KL, Yam C, Jain A, Krause PM, Lu Y, Cai S, Tu Y, Zhou X, Zhang X, Jiang Y, Carroll CL, Kang Z, Liu B, Shen J, Gagea M, Manu SM, Huo L, Gilcrease M, Powell RT, Guo L, Stephan C, Davies PJ, Parker-Thornburg J, Lozano G, Behringer RR, Piwnica-Worms H, Chang JT, Moulder SL, Barton MC. PMID: 34508101; PMCID: PMC8433435.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimals
    32. X-Linked Agammaglobulinemia and COVID-19: Two Case Reports and Review of Literature. Pediatr Allergy Immunol Pulmonol. 2021 Sep; 34(3):115-118. Devassikutty FM, Jain A, Edavazhippurath A, Joseph MC, Peedikayil MMT, Scaria V, Sandhya P, Govindaraj GM. PMID: 34495748; PMCID: PMC8664121.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    33. Robert's Uterus-Rare Cause of Intractable Dysmenorrhea and Chronic Pelvic Pain. J Hum Reprod Sci. 2021 Jul-Sep; 14(3):317-320. Nigam A, Basanti N, Sharma S, Gupta N, Jain A. PMID: 34759624; PMCID: PMC8527075.
      View in: PubMed   Mentions: 3  
    34. Vaginoscopic Incision of Oblique Vaginal Septum in an Adolescent Girl with OHVIRA Syndrome: Simple Management of Complicated Anomaly. J Hum Reprod Sci. 2021 Jul-Sep; 14(3):313-316. Nigam A, Aggarwal P, Baghel A, Gupta N, Sharma S, Jain A. PMID: 34759623; PMCID: PMC8527080.
      View in: PubMed   Mentions:
    35. An optimized, amplicon-based approach for sequencing of SARS-CoV-2 from patient samples using COVIDSeq assay on Illumina MiSeq sequencing platforms. STAR Protoc. 2021 Sep 17; 2(3):100755. Bhoyar RC, Senthivel V, Jolly B, Imran M, Jain A, Divakar MK, Scaria V, Sivasubbu S. PMID: 34368787; PMCID: PMC8326003.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    36. Whole genome sequencing identifies novel structural variant in a large Indian family affected with X-linked agammaglobulinemia. PLoS One. 2021; 16(7):e0254407. Jain A, Govindaraj GM, Edavazhippurath A, Faisal N, Bhoyar RC, Gupta V, Uppuluri R, Manakkad SP, Kashyap A, Kumar A, Divakar MK, Imran M, Sawant S, Dalvi A, Chakyar K, Madkaikar M, Raj R, Sivasubbu S, Scaria V. PMID: 34252140; PMCID: PMC8274882.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    37. Pharmacogenomic landscape of COVID-19 therapies from Indian population genomes. Pharmacogenomics. 2021 Jul; 22(10):603-618. Sahana S, Sivadas A, Mangla M, Jain A, Bhoyar RC, Pandhare K, Mishra A, Sharma D, Imran M, Senthivel V, Divakar MK, Rophina M, Jolly B, Batra A, Sharma S, Siwach S, Jadhao AG, Palande NV, Jha GN, Ashrafi N, Mishra PK, Vidhya AK, Jain S, Dash D, Kumar NS, Vanlallawma A, Sarma RJ, Chhakchhuak L, Kalyanaraman S, Mahadevan R, Kandasamy S, Devi P, Rajagopal RE, Ramya JE, Devi PN, Bajaj A, Gupta V, Mathew S, Goswami S, Prakash S, Joshi K, Kumla M, Sreedevi S, Gajjar D, Soraisham R, Yadav R, Devi YS, Gupta A, Mukerji M, Ramalingam S, Binukumar BK, Sivasubbu S, Scaria V. PMID: 34142560; PMCID: PMC8216321.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    38. Genomic survey of SARS-CoV-2 vaccine breakthrough infections in healthcare workers from Kerala, India. J Infect. 2021 08; 83(2):237-279. Philomina J B, Jolly B, John N, Bhoyar RC, Majeed N, Senthivel V, Cp F, Rophina M, Vasudevan B, Imran M, Viswanathan P, Arvinden VR, Joseph A, Divakar MK, Nair PR, Shamnath A, Kumar PJ, Jain A, Geetha P, Bajaj A, Mathew S, Gupta V, Agrawal SJ, Scaria V, Sivasubbu S, Radhakrishnan C. PMID: 34044037; PMCID: PMC8143909.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansCells
    39. Genetic Landscape of Rare Autoinflammatory Disease Variants in Qatar and Middle Eastern Populations Through the Integration of Whole-Genome and Exome Datasets. Front Genet. 2021; 12:631340. Sharma P, Jain A, Scaria V. PMID: 34054914; PMCID: PMC8155677.
      View in: PubMed   Mentions: 2  
    40. Symptomatic reinfection of SARS-CoV-2 with spike protein variant N440K associated with immune escape. J Med Virol. 2021 07; 93(7):4163-4165. Rani PR, Imran M, Lakshmi JV, Jolly B, Jain A, Surekha A, Senthivel V, Chandrasekhar P, Divakar MK, Srinivasulu D, Bhoyar RC, Vanaja PR, Scaria V, Sivasubbu S. PMID: 33818797; PMCID: PMC8250729.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
    41. Initial Insights Into the Genetic Epidemiology of SARS-CoV-2 Isolates From Kerala Suggest Local Spread From Limited Introductions. Front Genet. 2021; 12:630542. Radhakrishnan C, Divakar MK, Jain A, Viswanathan P, Bhoyar RC, Jolly B, Imran M, Sharma D, Rophina M, Ranjan G, Sehgal P, Jose BP, Raman RV, Kesavan TN, George K, Mathew S, Poovullathil JK, Keeriyatt Govindan SK, Nair PR, Vadekkandiyil S, Gladson V, Mohan M, Parambath FC, Mangla M, Shamnath A, Indian CoV2 Genomics & Genetic Epidemiology (IndiCovGEN) Consortium, Sivasubbu S, Scaria V. PMID: 33815467; PMCID: PMC8010186.
      View in: PubMed   Mentions: 14  
    42. Founder variants and population genomes-Toward precision medicine. Adv Genet. 2021; 107:121-152. Jain A, Sharma D, Bajaj A, Gupta V, Scaria V. PMID: 33641745.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansPHPublic Health
    43. High throughput detection and genetic epidemiology of SARS-CoV-2 using COVIDSeq next-generation sequencing. PLoS One. 2021; 16(2):e0247115. Bhoyar RC, Jain A, Sehgal P, Divakar MK, Sharma D, Imran M, Jolly B, Ranjan G, Rophina M, Sharma S, Siwach S, Pandhare K, Sahoo S, Sahoo M, Nayak A, Mohanty JN, Das J, Bhandari S, Mathur SK, Kumar A, Sahlot R, Rojarani P, Lakshmi JV, Surekha A, Sekhar PC, Mahajan S, Masih S, Singh P, Kumar V, Jose B, Mahajan V, Gupta V, Gupta R, Arumugam P, Singh A, Nandy A, P V R, Jha RM, Kumari A, Gandotra S, Rao V, Faruq M, Kumar S, Reshma G B, Varma G N, Roy SS, Sengupta A, Chattopadhyay S, Singhal K, Pradhan S, Jha D, Naushin S, Wadhwa S, Tyagi N, Poojary M, Scaria V, Sivasubbu S. PMID: 33596239; PMCID: PMC7888613.
      View in: PubMed   Mentions: 74     Fields:    Translation:HumansCellsPHPublic Health
    44. Six artificial intelligence paradigms for tissue characterisation and classification of non-COVID-19 pneumonia against COVID-19 pneumonia in computed tomography lungs. Int J Comput Assist Radiol Surg. 2021 Mar; 16(3):423-434. Saba L, Agarwal M, Patrick A, Puvvula A, Gupta SK, Carriero A, Laird JR, Kitas GD, Johri AM, Balestrieri A, Falaschi Z, Paschè A, Viswanathan V, El-Baz A, Alam I, Jain A, Naidu S, Oberleitner R, Khanna NN, Bit A, Fatemi M, Alizad A, Suri JS. PMID: 33532975; PMCID: PMC7854027.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCellsPHPublic Health
    45. IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes. Nucleic Acids Res. 2021 01 08; 49(D1):D1225-D1232. Jain A, Bhoyar RC, Pandhare K, Mishra A, Sharma D, Imran M, Senthivel V, Divakar MK, Rophina M, Jolly B, Batra A, Sharma S, Siwach S, Jadhao AG, Palande NV, Jha GN, Ashrafi N, Mishra PK, A K V, Jain S, Dash D, Kumar NS, Vanlallawma A, Sarma RJ, Chhakchhuak L, Kalyanaraman S, Mahadevan R, Kandasamy S, B M P, Rajagopal RE, J ER, P ND, Bajaj A, Gupta V, Mathew S, Goswami S, Mangla M, Prakash S, Joshi K, S S, Gajjar D, Soraisham R, Yadav R, Devi YS, Gupta A, Mukerji M, Ramalingam S, B K B, Scaria V, Sivasubbu S. PMID: 33095885; PMCID: PMC7778947.
      View in: PubMed   Mentions: 38     Fields:    Translation:Humans
    46. Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the SAMD12 gene. Brain Commun. 2021; 3(1):fcaa214. Mahadevan R, Bhoyar RC, Viswanathan N, Rajagopal RE, Essaki B, Suroliya V, Chelladurai R, Sankaralingam S, Shanmugam G, Vayanakkan S, Shamim U, Mathur A, Jain A, Imran M, Faruq M, Scaria V, Sivasubbu S, Kalyanaraman S. PMID: 33501421; PMCID: PMC7811760.
      View in: PubMed   Mentions: 5  
    47. Asymptomatic reactivation of SARS-CoV-2 in a child with neuroblastoma characterised by whole genome sequencing. IDCases. 2021; 23:e01018. Yadav SP, Thakkar D, Bhoyar RC, Jain A, Wadhwa T, Imran M, Jolly B, Divakar MK, Kapoor R, Rastogi N, Sharma D, Sehgal P, Ranjan G, Sivasubbu S, Sarma S, Scaria V. PMID: 33288996; PMCID: PMC7711173.
      View in: PubMed   Mentions: 6  
    48. Analysis of the potential impact of genomic variants in global SARS-CoV-2 genomes on molecular diagnostic assays. Int J Infect Dis. 2021 Jan; 102:460-462. Jain A, Rophina M, Mahajan S, Krishnan BB, Sharma M, Mandal S, Fernandez T, Sultanji S, Jolly B, Mathew S, Sivasubbu S, Scaria V. PMID: 33181329; PMCID: PMC7834429.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    49. Parental Experience of Hematopoietic Stem Cell Transplantation for Children with Primary Immune Deficiency Disorders. Indian J Pediatr. 2021 04; 88(4):370-371. Govindaraj GM, Ramya U, Raj R, Athulya EP, Jain A, Scaria V, Jayakrishnan MP, Sivasubbu S, Dhanasooraj D, Ajithkumar VT, Dongre AR, Krishnakumar P. PMID: 33095397.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    50. API-ISG Consensus Guidelines for Management of Gastrooesophageal Reflux Disease. J Assoc Physicians India. 2020 Oct; 68(10):69-80. Bhatia S, Pareek KK, Kumar A, Upadhyay R, Tiwaskar M, Jain A, Gupta P, Nadkar MY, Prakash A, Dutta A, Chavan R, Kedia S, Ahuja V, Ghoshal U, Agarwal A, Makharia G. PMID: 32978931.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    51. Spectrum of clinical features and genetic variants in mevalonate kinase (MVK) gene of South Indian families suffering from Hyperimmunoglobulin D Syndrome. PLoS One. 2020; 15(8):e0237999. Govindaraj GM, Jain A, Peethambaran G, Bhoyar RC, Vellarikkal SK, Ganapati A, Sandhya P, Edavazhippurath A, Dhanasooraj D, Puthenpurayil JM, Chakkiyar K, Mishra A, Batra A, Punnen A, Kumar S, Sivasubbu S, Scaria V. PMID: 32822427; PMCID: PMC7442240.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    52. Indian consensus on gastroesophageal reflux disease in adults: A position statement of the Indian Society of Gastroenterology. Indian J Gastroenterol. 2019 10; 38(5):411-440. Bhatia SJ, Makharia GK, Abraham P, Bhat N, Kumar A, Reddy DN, Ghoshal UC, Ahuja V, Rao GV, Devadas K, Dutta AK, Jain A, Kedia S, Dama R, Kalapala R, Alvares JF, Dadhich S, Dixit VK, Goenka MK, Goswami BD, Issar SK, Leelakrishnan V, Mallath MK, Mathew P, Mathew P, Nandwani S, Pai CG, Peter L, Prasad AVS, Singh D, Sodhi JS, Sud R, Venkataraman J, Midha V, Bapaye A, Dutta U, Jain AK, Kochhar R, Puri AS, Singh SP, Shimpi L, Sood A, Wadhwa RT. PMID: 31802441.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    53. Clinical profile and outcome of primary sclerosing cholangitis: A single-centre experience from western India. Indian J Gastroenterol. 2019 08; 38(4):295-302. Tibdewal P, Bhatt P, Jain A, Gupta D, Bhatia S, Shukla A. PMID: 31515764.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    54. Association of acute-on-chronic liver failure with vascular liver diseases. Hepatol Int. 2019 Jul; 13(4):399-402. Shukla A, Jain A. PMID: 31172418.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    55. Mutations in CYP2C9 and/or VKORC1 haplotype are associated with higher bleeding complications in patients with Budd-Chiari syndrome on warfarin. Hepatol Int. 2019 Mar; 13(2):214-221. Shukla A, Jain A, Kahalekar V, Bendkhale S, Gogtay N, Thatte U, Bhatia S. PMID: 30617764.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    56. Patients With Budd-Chiari Syndrome Have Variable Coagulation Status on Thromboelastography at Diagnosis. J Clin Exp Hepatol. 2019 Jul-Aug; 9(4):460-467. Jain A, Dhore P, Meshram M, Bhatia S, Shukla A. PMID: 31516262; PMCID: PMC6728540.
      View in: PubMed   Mentions: 4  
    57. Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India. Indian J Gastroenterol. 2018 03; 37(2):174-175. Jain A, Shukla A. PMID: 29616413.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    58. Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar. Mol Genet Genomics. 2018 Aug; 293(4):919-929. Jain A, Gandhi S, Koshy R, Scaria V. PMID: 29557500.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    59. Calreticulin mutations and their importance in Budd-Chiari syndrome. J Hepatol. 2017 11; 67(5):1111-1112. Jain A, Tibdewal P, Shukla A. PMID: 28662847.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    60. Recanalization of TIPSS via transsplenic puncture. Indian J Gastroenterol. 2017 May; 36(3):248-251. Jain A, Kahalekar V, Marar S, Gupta D, Sawrav S, Kiran S, Shukla A. PMID: 28577156.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    61. Study of clinical and aetiological profile of 100 patients of pancytopenia at a tertiary care centre in India. Hematology. 2012 Mar; 17(2):100-5. Doshi D, Shah AN, Somani S, Jain A, Jivarajani H, Kothari P. PMID: 22664048.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
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