Amanda Krause

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 20

Top Venues

European journal of human genetics : EJHG

Nature reviews. Neurology

Tremor and other hyperkinetic movements (New York, N.Y.)

Heart failure reviews

University of the Witwatersrand/NHLS

University of the Witwatersrand (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of the Witwatersrand/NHLS

South Africa

Head of Division/Medical Geneticist/Associate Professor :: Human Genetics

Education History

University of the Witwatersrand

South Africa

PHD :: Health Sciences

University of the Witwatersrand

South Africa

BSC :: Health Sciences

University of the Witwatersrand

South Africa

BSC :: Health Sciences

Publications

Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Abdoulaye Bocoum, Madani Ouologuem, Lassana Cissé, Fahmida Essop, Souleymane Papa Coulibaly, Nadine Botha, Cheick A K Cissé, Alassane Baneye Maiga, Amanda Krause, Guida Landouré, null null
The First Case of Huntington's Disease like 2 in Mali, West Africa. Tremor and other hyperkinetic movements (New York, N.Y.) 14 (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Amanda Krause, David G Anderson, Aline Ferreira-Correia, Jessica Dawson, Fiona Baine-Savanhu, Pan P Li, Russell L Margolis
Huntington disease-like 2: insight into neurodegeneration from an African disease. Nature reviews. Neurology (2023)
Nqoba Tsabedze, Michelle Ramsay, Amanda Krause, Quinn S Wells, Dineo Mpanya, Pravin Manga
The genetic basis for adult-onset idiopathic dilated cardiomyopathy in people of African descent. Heart failure reviews (2023)
Amanda Krause, David G Anderson, Aline Ferreira-Correia, Jessica Dawson, Fiona Baine-Savanhu, Pan P Li, Russell L Margolis
Huntington disease-like 2: insight into neurodegeneration from an African disease. Nature reviews. Neurology 20 (1) (2023)
Amanda Krause, David G Anderson, Aline Ferreira-Correia, Jessica Dawson, Fiona Baine-Savanhu, Pan P Li, Russell L Margolis
Huntington disease-like 2: insight into neurodegeneration from an African disease. Nature reviews. Neurology 20 (1) (2023)
Amanda Krause, David G Anderson, Aline Ferreira-Correia, Jessica Dawson, Fiona Baine-Savanhu, Pan P Li, Russell L Margolis
Huntington disease-like 2: insight into neurodegeneration from an African disease. Nature reviews. Neurology 20 (1) (2023)
Nqoba Tsabedze, Michelle Ramsay, Amanda Krause, Quinn S Wells, Dineo Mpanya, Pravin Manga
The genetic basis for adult-onset idiopathic dilated cardiomyopathy in people of African descent. Heart failure reviews (2023)
Bin Hashim Halim-Fikri, Carsten Werner Lederer, Atif Amin Baig, Siti Nor Assyuhada Mat-Ghani, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wardah Yusof, Diana Abdul Rashid, Nurul Fatihah Azman, Suthat Fucharoen, Ramdan Panigoro, Catherine Lynn T Silao, Vip Viprakasit, Norunaluwar Jalil, Norafiza Mohd Yasin, Rosnah Bahar, Veena Selvaratnam, Norsarwany Mohamad, Nik Norliza Nik Hassan, Ezalia Esa, Amanda Krause, Helen Robinson, Julia Hasler, Coralea Stephanou, Raja-Zahratul-Azma Raja-Sabudin, Jacques Elion, Ghada El-Kamah, Domenico A Coviello, Narazah Yusoff, Zarina Abdul Latiff, Chris Arnold, John Burn, Petros Kountouris, Marina Kleanthous, Raj Ramesar, Bin Alwi Zilfalil, null On Behalf Of The Global Globin Network Ggn
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries. Journal of personalized medicine 12 (4) (2022)
Laura Cottino, Venesa Sahibdeen, Maria Mudau, Nakedi Lekgate, Amanda Krause
QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa. Journal of community genetics 13 (3) (2022)
Nida Siddiqui, Faheem Seedat, Saajidah Bulbulia, Nompumelelo Zamokuhle Mtshali, Adam R Botha, Amanda Krause, Reyna Daya, Zaheer Bayat
SDHB-Associated Paraganglioma Syndrome in Africa-A Need for Greater Genetic Testing. Journal of the Endocrine Society 5 (10) (2021)
Kaitlyn Flynn, Candice Feben, Lindiwe Lamola, Nadia Carstens, Amanda Krause, Stephen Tollman, null null
Ending a diagnostic odyssey-The first case of Takenouchi-Kosaki syndrome in an African patient. Clinical case reports 9 (4) (2021)
Aline Ferreira-Correia, David G Anderson, Kate Cockcroft, Amanda Krause
A comparison between the neurocognitive profile of Huntington Disease-Like 2 and Huntington Disease: Exploring the presence of double dissociations. Applied neuropsychology. Adult (2020)
Shelley Macaulay, Quintin Clive Goodyear, Mia Kruger, Wenlong Carl Chen, Fahmida Essop, Amanda Krause
The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome. Familial cancer 17 (4) (2019)

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Publication Activity (10 Years)

Top Topics

Top Venues

Amanda Krause