Hannah Lewis

Medicine

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: “Parents Are the Experts: A Qualitative Study of the Experiences of Parents of Children With Severe Neurological Impairment During Decision-Making”.

Parents Are the Experts: A Qualitative Study of the Experiences of Parents of Children With Severe Neurological Impairment During Decision-Making

Journal of Pain and Symptom Management(2021)10.1016/j.jpainsymman.2021.06.011

N/A

0.624DataRank · unranked

63 citations

Amy Trowbridge, Hannah Lewis, Kelly J. Shipman, Danielle Jonas, Julie Hauer +2 more

Literacy-adapted, electronic family history assessment for genetics referral in primary care: patient user insights from qualitative interviews

Hereditary Cancer in Clinical Practice(2022)10.1186/s13053-022-00231-3

N/A

0.395DataRank · unranked

10 citations

Hannah Lewis, Devan M. Duenas, Donna J. Eubanks, Marian J. Gilmore, Katrina A.B. Goddard +12 more

Forming Clinician-Parent Therapeutic Alliance for Children With Severe Neurologic Impairment

Hospital Pediatrics(2022)10.1542/hpeds.2021-006316

N/A

0DataRank · unranked

23 citations

Amy Trowbridge, Hannah Lewis, Danielle Jonas, Julie Hauer, Abby R. Rosenberg +1 more

An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial

Genetics in Medicine(2022)10.1016/j.gim.2022.07.025

N/A

0DataRank · unranked

13 citations

Michael C. Leo, Leslie Riddle, Cláudia Guerra, Laura M. Amendola, Marian J. Gilmore +16 more

Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access

Genetics in Medicine(2022)10.1016/j.gim.2022.02.006

N/A

0DataRank · unranked

11 citations

Elizabeth Shuster, Michael C. Leo, Michael O. Dorschner, Bradley A. Rolf, Brian H. Shirts +73 more

Novel Interactors of the SH2 Domain of the Signaling Adaptors CRK and CRKL Identified in Neuro2A Cells

American Journal of Undergraduate Research(2022)10.33697/ajur.2022.068

N/A

0DataRank · unranked

2 citations

Anna M. Schmoker, Shannon M. Bennett, Amara Chittenden, Chelsea B Darwin, Helena Gaffney +10 more

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Genetics in Medicine(2023)10.1016/j.gim.2023.100923

N/A

0DataRank · unranked

15 citations

Leslie Riddle, Galen Joseph, Laura M. Amendola, Marian J. Gilmore, Jamilyn M. Zepp +73 more

Promoting equity, inclusion, and efficiency: A team science approach to the development of authorship guidelines for a multi-disciplinary research team

Journal of Clinical and Translational Science(2023)10.1017/cts.2023.685

N/A

0DataRank · unranked

4 citations

Barbara B. Biesecker, Sandra Soo‐Jin Lee, Katherine Anderson, Galen Joseph, Charisma L. Jenkins +5 more

Comparison of the Differing Impacts of Lowered N-Acetylglucosaminyltransferase-Ia/b Activity on Motor and Sensory Function in Zebrafish

International Journal of Translational Medicine(2025)10.3390/ijtm5030036

N/A

0DataRank · unranked

0 citations

Cody J. Hatchett, Haris Ali Khan, Hannah Lewis, Ruth A. Schwalbe, M. Kristen Hall

Patient perspectives on how to demonstrate respect: Implications for clinicians and healthcare organizations

PLoS ONE(2021)10.1371/journal.pone.0250999

N/A

0DataRank · unranked

17 citations

Devan M. Duenas, Hannah Lewis, Katherine Anderson, Douglas J. Opel, Benjamin S. Wilfond +2 more