Nara Sobreira

Johns Hopkins University

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: “The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities”.

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

The American Journal of Human Genetics(2015)10.1016/j.ajhg.2015.06.009

N/A

0.980DataRank · unranked

687 citations

Kati J. Buckingham, Shalini N. Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D. Smith +46 more

Microdeletions of 3q29 Confer High Risk for Schizophrenia

The American Journal of Human Genetics(2010)10.1016/j.ajhg.2010.07.013

N/A

0.819DataRank · unranked

234 citations

Anne F. Dodd, John A. McGrath, Paula S. Wolyniec, Adele A. Mitchell, Vivien Sheehan +14 more

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis

Human Molecular Genetics(2023)10.1093/hmg/ddad117

N/A

0DataRank · unranked

22 citations

Elizabeth Wohler, Vida Erfani, Guozhuang Li, Alexya N. Aguilera, Alberto Santiago-Cornier +11 more

Anxiety and dysautonomia symptoms in patients with a NaV1.7 mutation and the potential benefits of low-dose short-acting guanfacine

Clinical Autonomic Research(2023)10.1007/s10286-023-01004-1

N/A

0DataRank · unranked

8 citations

Maxime Lammens, Carley Blevins, Kristen Rodgers, Andrei Gurau, Suguru Yamauchi +13 more

CACNA1D is a circadian gene and causes familial advanced sleep phase

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2424387122

N/A

0DataRank · unranked

1 citations

Fayal Abderemane-Ali, Liza Ashbrook, Mingyang Ma, Neha Nibber, Xianlin Zou +7 more

Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan

Scientific Reports(2020)10.1038/s41598-020-68779-5

N/A

0DataRank · unranked

15 citations

Rasheeda Bashir, Midhat Salman, Ghulam Mujtaba, Nara Sobreira, P. Dane Witmer +2 more

Molecular characterization of recessively inherited ataxic and neuropathic disorders in consanguineous Pakistani families

Scientific Reports(2026)10.1038/s41598-026-37808-0

N/A

0DataRank · unranked

0 citations

Muhammad Wajid, Amina Iftikhar Butt, Elizabeth Wohler, Go Hun Seo, Weizhen Ji +7 more