Concepedia

Samantha Grieve

SG

Statistics

Publications

3

Citations

647

H-Index

3

Active since

2009

Affiliations

University of Cologne(Current)

Addenbrooke's Hospital

University of Freiburg

Universität Hamburg

University Medical Center Hamburg-Eppendorf

Samantha Grieve is an author at University of Cologne specializing in genetic disorders, genetics, and molecular genetics.

Publications per year

2009–2016

3

Publications

3

Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11

Udo zur Stadt, Jan Rohr, Wenke Seifert et al. · The American Journal of Human Genetics · 2009 · 415 citations · Full text

, , +9

Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome

Sandra Ammann, Ansgar Schulz, Ingeborg Krägeloh‐Mann et al. · Blood · 2016 · 177 citations · Full text

, , +12

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

Valentina Cetica, Yvonne Hackmann, Samantha Grieve et al. · Journal of Allergy and Clinical Immunology · 2014 · 55 citations · Full text

, , +16

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