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P. Gabrovska · SciRah

Researcher profile · Semantic Scholar

P. Gabrovska

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P. Gabrovska — researcher profile on SciRah

h-index: 13
Works: 31
Citations: 891

Most-cited papers

Heterogeneous Genetic Background of the Association of Pheochromocytoma/Paraganglioma and Pituitary Adenoma: Results From a Large Patient Cohort
J. Dénes, F. Swords, Eleanor Rattenberry, K. Stals +47 more
2014Journal of Clinical Endocrinology and Metabolism165 citations Open access
Semantic Scholar
Landscape of Familial Isolated and Young-Onset Pituitary Adenomas: Prospective Diagnosis in AIP Mutation Carriers
Laura C. Hernández-Ramírez, P. Gabrovska, J. Dénes, K. Stals +9 more
2015Journal of Clinical Endocrinology and Metabolism147 citations Open access
Semantic Scholar
MAFA missense mutation causes familial insulinomatosis and diabetes mellitus
D. Iacovazzo, S. Flanagan, E. Walker, Rosana Quezado +22 more
2018Proceedings of the National Academy of Sciences of the United States of America110 citations Open access
Semantic Scholar
A genetic variant located in miR-423 is associated with reduced breast cancer risk.
Robert A. Smith, Dominik J. Jedlinski, P. Gabrovska, S. Weinstein +2 more
2012Cancer Genomics & Proteomics79 citations
Semantic Scholar
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study
D. Iacovazzo, R. Caswell, B. Bunce, Sian Jose +31 more
2016Acta Neuropathologica Communications72 citations Open access
Semantic Scholar
Metformin to reduce metabolic complications and inflammation in patients on systemic glucocorticoid therapy: a randomised, double-blind, placebo-controlled, proof-of-concept, phase 2 trial.
I. Pernicova, S. Kelly, Sharon Ajodha, A. Sahdev +11 more
2020The Lancet Diabetes and Endocrinology70 citations Open access
Semantic Scholar
Germline or somatic GPR101 duplication leads to X-linked acrogigantism: a clinico-pathological and genetic study
D. Iacovazzo, R. Caswell, B. Bunce, Sian Jose +31 more
2016Acta Neuropathologica Communications54 citations Open access
Semantic Scholar
Single Nucleotide Polymorphism in hsa-mir-196a-2 and Breast Cancer Risk: A Case Control Study
Dominik J. Jedlinski, P. Gabrovska, S. Weinstein, Robert A. Smith +1 more
2011Twin Research and Human Genetics52 citations Open access
Semantic Scholar
Risk category system to identify pituitary adenoma patients with AIP mutations
F. Caimari, Laura C. Hernández-Ramírez, M. Dang, P. Gabrovska +4 more
2018Journal of Medical Genetics35 citations Open access
Semantic Scholar
Increased Population Risk of AIP‐Related Acromegaly and Gigantism in Ireland
S. Radian, Y. Diekmann, P. Gabrovska, B. Holland +44 more
2016Human Mutation26 citations Open access
Semantic Scholar
AIP mutations in young patients with acromegaly and the Tampico Giant: the Mexican experience
Claudia Ramírez-Rentería, Laura C. Hernández-Ramírez, L. Portocarrero-Ortiz, G. Vargas +19 more
2016Endocrine22 citations
Semantic Scholar
An unusual case of an ACTH-secreting macroadenoma with a germline variant in the aryl hydrocarbon receptor-interacting protein (AIP) gene
P. Dinesen, J. Dal, P. Gabrovska, M. Gaustadnes +6 more
2015Endocrinology, Diabetes & Metabolism Case Reports17 citations Open access
Semantic Scholar
In-frame seven amino-acid duplication in AIP arose over the last 3000 years, disrupts protein interaction and stability and is associated with gigantism
R. Salvatori, S. Radian, Y. Diekmann, D. Iacovazzo +22 more
2017European Journal of Endocrinology13 citations Open access
Semantic Scholar
Investigation of Two Wnt Signalling Pathway Single Nucleotide Polymorphisms in a Breast Cancer-Affected Australian Population
P. Gabrovska, Robert A. Smith, L. Haupt, L. Griffiths
2011Twin Research and Human Genetics13 citations Open access
Semantic Scholar
Gene Expression Profiling in Human Breast Cancer - Toward Personalised Therapeutics?
P. Gabrovska, Robert A. Smith, L. Haupt, L. Griffiths
20107 citations Open access
Semantic Scholar
Founder Effect in Recurring AIP Mutation Causing Familial Isolated Pituitary Adenoma Syndrome
R. Salvatori, P. Gabrovska, A. Weber, R. Quinton +14 more
20143 citations
Semantic Scholar
14th International workshop on multiple endocrine neoplasia and other rare endocrine tumors
E. Slater, M. Albers, R. Knoop, C. Lopez +20 more
2014Wiener Klinische Wochenschrift2 citations
Semantic Scholar
RET mutation negative familial medullary thyroid carcinoma: four families and literature review
D. Iacovazzo, P. Morrison, W. Foulkes, D. Ross +6 more
20142 citations
Semantic Scholar
ESR2 mutations in RET mutation-negative familial medullary thyroid carcinoma
Wazir K. Afghan, D. Iacovazzo, M. Alevizaki, W. Foulkes +11 more
20161 citations
Semantic Scholar
The burden of AIP mutations in pituitary adenoma patients from the UK
F. Caimari, M. Dang, P. Gabrovska, Laura C. Hernández-Ramírez +16 more
20151 citations
Semantic Scholar
Pituitary adenoma and phaeochromocytoma/paraganglioma [ndash] a novel syndrome with a heterogeneous genetic background
J. Dénes, F. Swords, Eleanor Rattenberry, P. Xekouki +33 more
20131 citations
Semantic Scholar
Gene Expression Analysis in Human Breast Cancer
P. Gabrovska
20121 citations
Semantic Scholar
A MAFA missense mutation causes familial insulinomatosis and diabetes mellitus 1 2
D. Iacovazzo, S. Flanagan, E. Walker, Rosana Quezado +23 more
20180 citations
Semantic Scholar
Single Nucleotide Polymorphism in hsa mir 196 a 2 and Breast Cancer Risk : A Case Control
Dominik J. Jedlinski, P. Gabrovska, S. Weinstein, Robert A. Smith +1 more
20170 citations
Semantic Scholar
A missense mutation in the islet-enriched transcription factor MAFA leads to familial insulinomatosis and diabetes
D. Iacovazzo, S. Flanagan, E. Walker, R. Caswell +16 more
20160 citations
Semantic Scholar
Unique clinical picture in patients with X-linked acrogigantism
D. Iacovazzo, Sian Jose, B. Bunce, R. Caswell +20 more
20150 citations
Semantic Scholar
The founder R304* AIP mutation is prevalent in Irish acromegaly and gigantism patients as well as in the general population of Ireland
S. Radian, Y. Diekmann, P. Gabrovska, B. Holland +44 more
20150 citations
Semantic Scholar
Population Screening for the Irish Founder AIP Mutation R304*Reveals a Prevalence of 1/500 in the Local Population, While High Mutation Frequency Is Present Among Irish Familial and Sporadic Somatotropinoma Patients
S. Radian, P. Gabrovska, B. Holland, H. Wallace +29 more
20140 citations
Semantic Scholar
Genetic and clinical characteristics of Serbian FIPA families
D. Miljić, S. Pekic, M. Stojanović, N. Dzeranova +4 more
20130 citations
Semantic Scholar
Creation of a locus-specific database for AIP mutations
Fauzia Begum, G. Trivellin, P. Gabrovska, Katarzyna Wertheim Tysarowska +5 more
20130 citations Open access
Semantic Scholar
Single Nucleotide Polymorphism in hsa mir 196 a 2 and Breast Cancer Risk :
Dominik J. Jedlinski, P. Gabrovska, S. Weinstein, Robert A. Smith +1 more
20120 citations
Semantic Scholar

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M. Korbonits×23
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Laura C. Hernández-Ramírez

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