Nikita R. Dsouza

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “POLD1 Deficiency Reveals a Role for POLD1 in DNA Repair and T and B Cell Development”.

POLD1 Deficiency Reveals a Role for POLD1 in DNA Repair and T and B Cell Development

Journal of Clinical Immunology(2020)10.1007/s10875-020-00903-6

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0DataRank · unranked

20 citations

Ottavia M. Delmonte, Vanessa Bundy, Marita Bosticardo, Michael T. Zimmermann, Nikita R. Dsouza +12 more

Interaction between Mas1 and AT1RA contributes to enhancement of skeletal muscle angiogenesis by angiotensin-(1-7) in Dahl salt-sensitive rats

PLoS ONE(2020)10.1371/journal.pone.0232067

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0DataRank · unranked

11 citations

Aron M. Geurts, Brian Hoffmann, Marc Casati, Timothy J. Stodola, Nikita R. Dsouza +4 more

Structural bioinformatics enhances mechanistic interpretation of genomic variation, demonstrated through the analyses of 935 distinct RAS family mutations

Bioinformatics(2020)10.1093/bioinformatics/btaa972

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0DataRank · unranked

12 citations

Nikita R. Dsouza, Raúl Urrutia, Michael T. Zimmermann, Swarnendu Tripathi

Impairment of the mitochondrial one-carbon metabolism enzyme SHMT2 causes a novel brain and heart developmental syndrome

Acta Neuropathologica(2020)10.1007/s00401-020-02223-w

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0DataRank · unranked

46 citations

Edgard Verdura, Natalia Juliá‐Palacios, Eric N. Anderson, Leire Goicoechea, Laura Planas‐Serra +33 more

A homozygous missense variant in UBE2T is associated with a mild Fanconi anemia phenotype

Haematologica(2020)10.3324/haematol.2020.259275

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0DataRank · unranked

5 citations

Francis P. Lach, Kimberly A. Rickman, Alejandro Ferrer, Abhishek A. Mangaonkar, Tanya L. Schwab +10 more

Discovery, expression, cellular localization, and molecular properties of a novel, alternative spliced HP1γ isoform, lacking the chromoshadow domain

PLoS ONE(2020)10.1371/journal.pone.0217452

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0DataRank · unranked

7 citations

Thiago M. de Assuncao, Nikita R. Dsouza, Monique Williams, Michael T. Zimmermann, Raúl Urrutia +2 more

SASH3variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation

Blood(2021)10.1182/blood.2020008629

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0DataRank · unranked

56 citations

Jenna Bergerson, Tomoki Kawai, Hye Sun Kuehn, David H. McDermott, Irene Cortese +30 more

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability

Journal of Medical Genetics(2021)10.1136/jmedgenet-2021-107751

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0DataRank · unranked

30 citations

Margot A. Cousin, Nikita R. Dsouza, Thomas D. Challman, Karen E. Wain, Zöe Powis +67 more

Enhanced interpretation of 935 hotspot and non-hotspot RAS variants using evidence-based structural bioinformatics

Computational and Structural Biotechnology Journal(2021)10.1016/j.csbj.2021.12.007

N/A

0DataRank · unranked

10 citations

Nikita R. Dsouza, Angela Mathison, Elise Leverence, Raúl Urrutia, Michael T. Zimmermann +1 more

Computational modeling reveals key molecular properties and dynamic behavior of disruptor of telomeric silencing 1‐like ( DOT1L ) and partnering complexes involved in leukemogenesis

Proteins Structure Function and Bioinformatics(2021)10.1002/prot.26219

N/A

0DataRank · unranked

5 citations

Young‐In Chi, Thiago M. de Assuncao, Elise Leverence, Swarnendu Tripathi, Nikita R. Dsouza +7 more