Joan Jasien

Also affiliated with Duke University Hospital

MedicineBiochemistry, Genetics and Molecular Biology

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 8 papers. Top paper: “Epileptic encephalopathy with features of rapid‐onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation”.

Epileptic encephalopathy with features of rapid‐onset dystonia Parkinsonism and alternating hemiplegia of childhood: a novel combination phenotype associated with ATP1A3 mutation

Epileptic Disorders(2020)10.1684/epd.2020.1127

N/A

0DataRank · unranked

9 citations

Jason Richards, Marie McDonald, Allyn McConkie‐Rosell, Nicholas Stong, Joan Jasien +3 more

Cognitive and motor function in adults with spina bifida myelomeningocele: a pilot study

IAS(2020)10.1007/s00381-020-04964-1

N/A

0DataRank · unranked

5 citations

Mohamad A. Mikati, Michaela Kolářová, Brian N. Smith, Stephanie Thera, Pierre Lee +1 more

Opportunities, barriers, and recommendations in Down syndrome research

Translational Science of Rare Diseases(2021)10.3233/trd-200090

N/A

0DataRank · unranked

100 citations

Angelika Amon, Leonard Abbeduto, Stamatis Agiovlasitis, Tarek Alsaied, Heather A. Anderson +47 more

Rare deleterious de novo missense variants in Rnf2/Ring2 are associated with a neurodevelopmental disorder with unique clinical features

Human Molecular Genetics(2021)10.1093/hmg/ddab110

N/A

0DataRank · unranked

29 citations

Kelly Schoch, Sharayu Jangam, Venkata Hemanjani Bhavana, Hillary K. Graves, Sujay Kansagra +11 more

Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations

Epilepsy & Behavior(2021)10.1016/j.yebeh.2020.107732

N/A

0DataRank · unranked

28 citations

David M. Mueller, Milton Pratt, Melanie Bonner, Courtney Elliott, Arsen Hunanyan +9 more

The microRNA processorDROSHAis a candidate gene for a severe progressive neurological disorder

Human Molecular Genetics(2022)10.1093/hmg/ddac085

N/A

0DataRank · unranked

17 citations

Mümine Şentürk, Kelly Schoch, Amanda L. Minogue, Diego Lopergolo, Chiara Fallerini +95 more

Variation in Neurodegeneration‐Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida

Annals of the Child Neurology Society(2025)10.1002/cns3.70016

N/A

0DataRank · unranked

0 citations

Jacques Stout, Mohamad A. Mikati, Robert J. Anderson, Brittany Nave, Herbert E. Fuchs +4 more

Sequencing Analysis Demonstrates That a Complex Genetic Architecture Contributes to Risk for Spina Bifida

Birth Defects Research(2025)10.1002/bdr2.2533

N/A

0DataRank · unranked

0 citations

Melanie E. Garrett, Max Bucklan, Joan Jasien, Gordon Worley, Christopher A. Walsh +2 more