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Gayatri Ramakrishnan

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Tuberculosis (Edinburgh, Scotland)|December 4, 2014
Enriching the annotation of Mycobacterium tuberculosis H37Rv proteome using remote homology detection approaches: insights into structure and functionGayatri Ramakrishnan, Bernardo Ochoa-Montaño, Upadhyayula S Raghavender, et al.
Database : the Journal of Biological Databases and Curation|July 2, 2015
SInCRe-structural interactome computational resource for Mycobacterium tuberculosisRahul Metri, Sridhar Hariharaputran, Gayatri Ramakrishnan, et al.
Briefings in Bioinformatics|June 15, 2026
SwiftTCR: efficient computational docking protocol of TCRpMHC-I complexes using restricted rotation matricesFarzaneh M Parizi, Yannick J M Aarts, Nils Smit, et al.
Human Genetics|October 15, 2024
Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved casesHedwig M Velde, Maryam Vaseghi-Shanjani, Jeroen J Smits, et al.
Nature Communications|April 10, 2024
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residuesKian Hong Kock, Patrick K Kimes, Stephen S Gisselbrecht, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Complexome profiling showed impaired immunoproteasome assembly in a novel PRAAS subtype caused by monoallelic PSMB8 variantsRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.
American Journal of Human Genetics|March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndromeCaspar I van der Made, Simone Kersten, Odelia Chorin, et al.
American Journal of Human Genetics|May 21, 2026
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assemblyRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Tuberculosis (Edinburgh, Scotland)|December 4, 2014
Enriching the annotation of Mycobacterium tuberculosis H37Rv proteome using remote homology detection approaches: insights into structure and functionGayatri Ramakrishnan, Bernardo Ochoa-Montaño, Upadhyayula S Raghavender, et al.
Database : the Journal of Biological Databases and Curation|July 2, 2015
SInCRe-structural interactome computational resource for Mycobacterium tuberculosisRahul Metri, Sridhar Hariharaputran, Gayatri Ramakrishnan, et al.
Briefings in Bioinformatics|June 15, 2026
SwiftTCR: efficient computational docking protocol of TCRpMHC-I complexes using restricted rotation matricesFarzaneh M Parizi, Yannick J M Aarts, Nils Smit, et al.
Human Genetics|October 15, 2024
Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved casesHedwig M Velde, Maryam Vaseghi-Shanjani, Jeroen J Smits, et al.
Nature Communications|April 10, 2024
DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residuesKian Hong Kock, Patrick K Kimes, Stephen S Gisselbrecht, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Complexome profiling showed impaired immunoproteasome assembly in a novel PRAAS subtype caused by monoallelic PSMB8 variantsRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.
American Journal of Human Genetics|March 19, 2024
Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndromeCaspar I van der Made, Simone Kersten, Odelia Chorin, et al.
American Journal of Human Genetics|May 21, 2026
Monoallelic PSMB8 variants cause PRAAS with immunodeficiency through impaired immunoproteasome assemblyRobin Wijngaard, Caspar I van der Made, Sema Kalkan Uçar, et al.
Pageof 2