Amanda Krause

Also affiliated with University of the Witwatersrand

NeuroscienceBiochemistry, 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 11 papers. Top paper: “Randomized Controlled Trial of Upper Esophageal Sphincter Assist Device in Laryngopharyngeal Reflux Disease”.

Randomized Controlled Trial of Upper Esophageal Sphincter Assist Device in Laryngopharyngeal Reflux Disease

Clinical Gastroenterology and Hepatology(2025)10.1016/j.cgh.2025.12.015

N/A

0.104DataRank · unranked

1 citations

Lorijane Robles, Mary Clarke, Eric E. Low, Erin Walsh, Amanda Krause +2 more

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

Genetics in Medicine(2022)10.1016/j.gim.2022.05.001

N/A

0DataRank · unranked

25 citations

Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret L. Bostwick +36 more

Genetic services in a resource-constrained African setting – diagnostic odysseys, limited testing strategies and the need for exome sequencing

Research Square(2022)10.21203/rs.3.rs-1738191/v1

N/A

0DataRank · unranked

0 citations

J. Buchanan, Zané Lombard, Amanda Krause, Emma K. Wiener

Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100244

N/A

0DataRank · unranked

7 citations

Cíntia Fridman, Bonald C. Figueiredo, Hector Salvador, Manuel R. Teixeira, Carla Pinto +23 more

Identifying the genetic causes of developmental disorders and intellectual disability in Africa: a systematic literature review

Frontiers in Genetics(2023)10.3389/fgene.2023.1137922

N/A

0DataRank · unranked

6 citations

Shelley Macaulay, N. Louw, Alanna Bollweg, Kaitlyn Flynn, Mhlekazi Molatoli +6 more

Research participants' perspectives regarding the feedback of secondary findings–A cohort from the DDD‐Africa study, South Africa

Journal of Genetic Counseling(2023)10.1002/jgc4.1830

N/A

0DataRank · unranked

0 citations

Bianca Rossouw, Jamey Thom, N. Louw, Amanda Krause, Zané Lombard +1 more

STAC3 disorder: a common cause of congenital hypotonia in Southern African patients

European Journal of Human Genetics(2024)10.1038/s41431-024-01644-5

N/A

0DataRank · unranked

9 citations

Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie +12 more

The First Case of Huntington’s Disease like 2 in Mali, West Africa

Tremor and Other Hyperkinetic Movements(2024)10.5334/tohm.859

N/A

0DataRank · unranked

2 citations

M Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha +5 more

Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients

European Journal of Human Genetics(2024)10.1038/s41431-024-01669-w

N/A

0DataRank · unranked

1 citations

Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie +12 more

Ending a diagnostic odyssey—The first case of Takenouchi–Kosaki syndrome in an African patient

Clinical Case Reports(2021)10.1002/ccr3.3966

N/A

0DataRank · unranked

14 citations

Candice Feben, Lindiwe Lamola, Nadia Carstens, Amanda Krause, Zané Lombard +1 more

A training program to extend the reach of the deciphering developmental disorders in Africa (DDD-Africa) study

Frontiers in Genetics(2025)10.3389/fgene.2025.1611047

N/A

0DataRank · unranked

0 citations

Zané Lombard, Nadia Carstens, Zandisiwe Goliath, Aimé Lumaka, Prince Makay +6 more