Tarekegn Geberhiwot - Concepedia

Author

Tarekegn Geberhiwot

Also Known As

Barry J. Byrne, Bojan Vujkovac, Geberhiwot, Tarekegn, T D Geberhiwot, T Geberhiwot, T. Geberhiwot, Tarekegn Geberhiwot, Tarekegn Hiwot, on behalf of the International Niemann-Pick Disease Registry (INPDR)

182

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University of Birmingham Queen Elizabeth Hospital Birmingham University College London University Hospitals Birmingham NHS Foundation Trust NIHR Surgical Reconstruction and Microbiology Research Centre

About

Tarekegn Geberhiwot is an author at University of Birmingham specializing in medicine, molecular biology, and cell signaling.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	314
2	Health Sciences	2	2	41
3	Natural Sciences	2	2	198
4	Language Studies	1	1	23
5	Social Sciences	1	1	23

Tarekegn Geberhiwot

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document Marieke Biegstraaten, Reynir Arngrı́msson, Frédéric Barbey, Orphanet Journal of Rare Diseases	2015	335
Origin and Diffusion of mtDNA Haplogroup X Maere Reidla, Toomas Kivisild, Ene Metspalu, The American Journal of Human Genetics Mtdna Haplogroup XDnaCytogeneticsNatural SciencesGenetics	2003	182
The impact of phenylalanine levels on cognitive outcomes in adults with phenylketonuria: Effects across tasks and developmental stages. Cristina Romani, Liana Palermo, Anita MacDonald, Neuropsychology	2017	113
Interim analyses of a first-in-human phase 1/2 mRNA trial for propionic acidaemia Dwight D. Koeberl, Andreas Schulze, Neal Sondheimer, Nature	2024	106
Cognitive outcomes in early-treated adults with phenylketonuria (PKU): A comprehensive picture across domains. Liana Palermo, Tarekegn Geberhiwot, Anita MacDonald, Neuropsychology	2017	96
Cardiac Phenotype of Prehypertrophic Fabry Disease Sabrina Nordin, Rebecca Kozor, Shanat Baig, Circulation Cardiovascular Imaging	2018	89
Myocardial Edema, Myocyte Injury, and Disease Severity in Fabry Disease João B. Augusto, Sabrina Nordin, Ravi Vijapurapu, Circulation Cardiovascular Imaging	2020	85
High quality, patient centred and coordinated care for Alstrom syndrome: a model of care for an ultra-rare disease Stephanie Van Groenendael, Luca Giacovazzi, Fabian Davison, Orphanet Journal of Rare Diseases	2015	79
Consensus clinical management guidelines for acid sphingomyelinase deficiency (Niemann–Pick disease types A, B and A/B) Tarekegn Geberhiwot, Melissa Wasserstein, Subadra Wanninayake, Orphanet Journal of Rare Diseases	2023	76
An endothelial laminin isoform, laminin 8 (α4β1γ1), is secreted by blood neutrophils, promotes neutrophil migration and extravasation, and protects neutrophils from apoptosis Zenebech Wondimu, Tarekegn Geberhiwot, Sulev Ingerpuu, Blood	2004	74

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