Selinda Mascarenhas

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 7 papers. Top paper: “De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India”.

De novo variants underlying monogenic syndromes with intellectual disability in a neurodevelopmental cohort from India

European Journal of Human Genetics(2023)10.1038/s41431-023-01513-7

N/A

0DataRank · unranked

19 citations

Purvi Majethia, Karthik Vijay Nair, Lakshmi Priya Rao, Selinda Mascarenhas, Namanpreet Kaur +26 more

Further validation of craniosynostosis as a part of phenotypic spectrum of BCL11B‐related BAFopathy

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63330

N/A

0DataRank · unranked

5 citations

Selinda Mascarenhas, A. Venkatraman, Vivekananda Bhat, Dhanya Lakshmi Narayanan, Shahyan Siddiqui +4 more

Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implications

Clinical Genetics(2024)10.1111/cge.14495

N/A

0DataRank · unranked

7 citations

Namanpreet Kaur, Selinda Mascarenhas, Lakshmi Priya Rao, Shruti Pande, Dhanya Lakshmi Narayanan +27 more

Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63914

N/A

0DataRank · unranked

2 citations

Michelle C. do Rosario, Purvi Majethia, Selinda Mascarenhas, Lakshmi Priya Rao, Karthik Vijay Nair +17 more

Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological Disorder

Clinical Genetics(2024)10.1111/cge.14663

N/A

0DataRank · unranked

2 citations

Neha Quadri, Florian Erger, Nico Fuhrmann, Otilia‐Maria Geist, Christian Netzer +10 more

Report of a novel recurrent homozygous variant c.620A>T in three unrelated families with thiamine metabolism dysfunction syndrome 5 and review of literature

Clinical Dysmorphology(2024)10.1097/mcd.0000000000000490

N/A

0DataRank · unranked

1 citations

Mayuri Yeole, Lakshmi Priya Rao, Michelle C. do Rosario, Purvi Majethia, Karthik Vijay Nair +7 more

c.202_204del in NUP214 causes late onset form of febrile encephalopathy

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63529

N/A

0DataRank · unranked

1 citations

Dhanya Lakshmi Narayanan, Selinda Mascarenhas, Michelle C. do Rosario, Karthik Vijay Nair, Radhakrishnan Periyasamy +2 more