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Stayko Sarafov · SciRah

Researcher profile · Semantic Scholar

Stayko Sarafov

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Stayko Sarafov — researcher profile on SciRah

h-index: 13
Works: 25
Citations: 938

Most-cited papers

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
J. van der Zee, I. Gijselinck, Lubina Dillen, T. Van Langenhove +58 more
2012Human Mutation285 citations Open access
Semantic Scholar
Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations*
I. Conceição, T. Damy, M. Romero, L. Galán +6 more
2019Amyloid: Journal of Protein Folding Disorders174 citations Open access
Semantic Scholar
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
J. van der Zee, T. Van Langenhove, G. Kovacs, Lubina Dillen +76 more
2014Acta Neuropathologica116 citations Open access
Semantic Scholar
TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis
J. van der Zee, I. Gijselinck, S. Van Mossevelde, F. Perrone +77 more
2017Human Mutation101 citations Open access
Semantic Scholar
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients.
Lubina Dillen, T. Van Langenhove, S. Engelborghs, M. Vandenbulcke +10 more
2013Neurobiology of Aging45 citations Open access
Semantic Scholar
Peripheral nerve ultrasonography in patients with transthyretin amyloidosis.
S. Podnar, Stayko Sarafov, I. Tournev, G. Omejec +1 more
2017Clinical Neurophysiology40 citations
Semantic Scholar
Two consecutive pregnancies in early and late stage of amyotrophic lateral sclerosis
Stayko Sarafov, Maryana K Doitchinova, Zhvka Karagiozova, B. Slancheva +3 more
2009Amyotrophic Lateral Sclerosis23 citations
Semantic Scholar
Founder effect of the Glu89Gln TTR mutation in the Bulgarian population
A. Kirov, Stayko Sarafov, Zornitza Pavlova, T. Todorov +5 more
2019Amyloid: Journal of Protein Folding Disorders22 citations
Semantic Scholar
L239F founder mutation in GDAP1 is associated with a mild Charcot–Marie–Tooth type 4C4 (CMT4C4) phenotype
D. Kabzińska, H. Strugalska-Cynowska, A. Kostera-Pruszczyk, B. Ryniewicz +14 more
2010Neurogenetics22 citations
Semantic Scholar
Transthyretin Amyloidosis: Testing Strategies And Model for Center of Excellence Support.
R. Nakov, Stayko Sarafov, M. Gospodinova, A. Kirov +4 more
2020Clinica chimica acta; international journal of clinical chemistry14 citations
Semantic Scholar
Clinical trials in pediatric ALS: a TRICALS feasibility study
Tessa Kliest, R. V. van Eijk, A. Al-Chalabi, A. Albanese +53 more
2022Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration13 citations Open access
Semantic Scholar
Cardiac involvement, morbidity and mortality in hereditary transthyretin amyloidosis because of p.Glu89Gln mutation.
M. Gospodinova, Stayko Sarafov, T. Chamova, A. Kirov +5 more
2020Journal of Cardiovascular Medicine13 citations
Semantic Scholar
Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations
R. Nakov, O. Suhr, G. Ianiro, J. Kupčinskas +10 more
2020European Journal of Gastroenterology and Hepathology13 citations
Semantic Scholar
Fecal calprotectin levels are elevated in transthyretin amyloidosis patients with gastrointestinal manifestations
R. Nakov, Stayko Sarafov, V. Nakov, M. Gospodinova +4 more
2020Medicine10 citations Open access
Semantic Scholar
Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln Mutation.
R. Nakov, Stayko Sarafov, V. Nakov, M. Gospodinova +4 more
2019Journal of Gastrointestinal and Liver Diseases10 citations Open access
Semantic Scholar
Clinical Spectrum and Genetic Variability in Bulgarian Patients with Niemann-Pick Disease Type C
T. Chamova, A. Kirov, V. Guergueltcheva, T. Todorov +9 more
2016European Neurology10 citations
Semantic Scholar
Transthyretin Amyloidosis with Gastrointestinal Manifestation: a Case Report.
R. Nakov, Stayko Sarafov, V. Nakov, M. Gospodinova +4 more
2019Journal of Gastrointestinal and Liver Diseases7 citations Open access
Semantic Scholar
Characterization of population genetic structure of hereditary transthyretin amyloidosis in Bulgaria
Z. Pavlova, Stayko Sarafov, T. Todorov, A. Kirov +5 more
2021Amyloid: Journal of Protein Folding Disorders6 citations
Semantic Scholar
Monoallelic expression of the TTR gene as a contributor to the age at onset and penetrance of TTR-related amyloidosis.
I. Yordanova, Zornitza Pavlova, A. Kirov, T. Todorov +8 more
2019Gene6 citations
Semantic Scholar
Epidemiology of Familial Amyloid Polyneuropathy in Bulgaria
Stayko Sarafov, M. Gospodinova, Velina Guergueltcheva Velina, A. Kirov +4 more
2015Orphanet Journal of Rare Diseases3 citations Open access
Semantic Scholar
Fecal calprotectin concentrations in patients with hereditary transthyretin amyloidosis and gastrointestinal symptoms.
R. Nakov, Stayko Sarafov, V. Nakov, M. Gospodinova +1 more
2020European Journal of Gastroenterology and Hepathology2 citations
Semantic Scholar
Diagnostic algorithm in transthyretin amyloidosis with cardiomyopathy
M. Gospodinova, E. Kinova, I. Simova, Y. Yotov +8 more
20202 citations Open access
Semantic Scholar
Cardiomyopathy and peripheral polyneuropathy severity in patients with Glu89Gln mutation at the time of diagnosis
M. Gospodinova, Stayko Sarafov, V. Guergueltcheva, A. Kirov +4 more
2015Orphanet Journal of Rare Diseases2 citations Open access
Semantic Scholar
Cardiac involvement and clinical follow up of patients with hereditary transthyretin related amyloidosis associated with Glu89Gln mutation
M. Gospodinova, Stayko Sarafov, V. Guergueltcheva, A. Kirov +4 more
2015Orphanet Journal of Rare Diseases1 citations Open access
Semantic Scholar
TBK1 loss-of function and dominant-negative mutations in an extended European cohort of FTD and ALS patients
J. van der Zee, I. Gijselinck, S. Van Mossevelde, F. Perrone +35 more
20160 citations
Semantic Scholar

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