Azita Sadeghpour

Also affiliated with PragmatIC (United Kingdom), Duke Medical Center, Duke University Hospital

Biochemistry, Genetics and Molecular BiologyMedicine

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: “Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy”.

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

Nature Genetics(2020)10.1038/s41588-020-0707-1

N/A

2.0DataRank · unranked

35 citations

Onuralp Söylemez, Aysegül Ozanturk, Niki Mourtzi, Sebastian Akle, Irwin Jungreis +16 more

Implementing a pragmatic clinical trial to tailor opioids for acute pain on behalf of the IGNITE ADOPT PGx investigators

Clinical and Translational Science(2022)10.1111/cts.13376

N/A

0.650DataRank · unranked

22 citations

Emily J. Cicali, Kristin Wiisanen, Roger B. Fillingim, Hrishikesh Chakraborty, Rachel A. Myers +35 more

Establishing the value of genomics in medicine: the IGNITE Pragmatic Trials Network

Genetics in Medicine(2021)10.1038/s41436-021-01118-9

N/A

0.529DataRank · unranked

33 citations

Larisa H. Cavallari, Hrishikesh Chakraborty, Rhonda M. Cooper‐DeHoff, Paul Dexter, Michael T. Eadon +51 more

Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/362707

N/A

0.403DataRank · unranked

4 citations

Onuralp Söylemez, Aysegül Ozanturk, Sebastian Akle, Irwin Jungreis, Jean Muller +16 more

Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancer

Contemporary Clinical Trials(2024)10.1016/j.cct.2024.107714

N/A

0.261DataRank · unranked

4 citations

Harris T. Bland, Justin Andujar, Natasha Celaya‐Cobbs, Clasherrol Edwards, Meredith Gerhart +12 more

A case of Bardet‑Biedl syndrome caused by a recurrent variant inBBS12: A case report

Biomedical Reports(2021)10.3892/br.2021.1479

N/A

0DataRank · unranked

10 citations

Magdalena Budișteanu, Carmen Burloiu, Sheraz Khan, Azita Sadeghpour, Laurențiu Camil Bohîlțea +3 more

Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

Genetics in Medicine(2023)10.1016/j.gim.2023.100897

N/A

0DataRank · unranked

10 citations

Kelly Schoch, Rebecca Ganetzky, Peter G. Kranz, Neal Sondheimer, M. Louise Markert +92 more