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» Authors » Jordi Rosell Andreo

Jordi Rosell Andreo

Explore the profile of Jordi Rosell Andreo including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 5
Citations 66
Followers 0
Related Specialties
Genetics
Cardiology & Vascular Diseases
Neurology
Top 10 Co-Authors
Ramona Alfaro Arenas
Nancy Govea Callizo
Damian Heine Suner
Michael J Owen
Beverly S Emanuel
Martin Ortiz
Lorenzo Socias Crespi
Abraham Weizman
Line Olsen
Maude Schneider
Published In
Int J Cardiol
J Genet Couns
Am J Hum Genet
Rev Esp Cardiol (Engl Ed)
Am J Med Genet B Neuropsychiatr Genet
Affiliations
Soon will be listed here.
Recent Articles
1.
Sudden cardiac death in persons aged 50 years or younger: diagnostic yield of a regional molecular autopsy program using massive sequencing
Ripoll-Vera T, Perez Luengo C, Borondo Alcazar J, Garcia Ruiz A, Sanchez Del Valle N, Barcelo Martin B, et al.
Rev Esp Cardiol (Engl Ed) . 2020 Sep; 74(5):402-413. PMID: 32917565
Introduction And Objectives: Sudden cardiac death (SCD) in young people often has a genetic cause. Consequently, the results of "molecular autopsy" may have important implications for their relatives. Our objective...
2.
A Pilot Study of Fragile X Syndrome Screening in Pregnant Women and Women Planning Pregnancy: Implementation, Acceptance, Awareness, and Geographic Factors
Alfaro Arenas R, Rosell Andreo J, Suner D
J Genet Couns . 2016 Oct; 26(3):501-510. PMID: 27714485
We report herein results of a study performed in the Balearic Islands which had the following goals: 1) Determine the proportion of pregnant or non-pregnant women planning pregnancy, who would...
3.
Fragile X syndrome screening in pregnant women and women planning pregnancy shows a remarkably high FMR1 premutation prevalence in the Balearic Islands
Alfaro Arenas R, Rosell Andreo J, Heine Suner D
Am J Med Genet B Neuropsychiatr Genet . 2016 Jun; 171(8):1023-1031. PMID: 27333191
There are no reported studies to determine incidence of Fragile X Syndrome (FXS) in women within the Spanish population. For this reason, together with the high incidence of FXS in...
4.
Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes
Delio M, Guo T, McDonald-McGinn D, Zackai E, Herman S, Kaminetzky M, et al.
Am J Hum Genet . 2013 Mar; 92(3):439-47. PMID: 23453669
Velocardiofacial and DiGeorge syndromes, also known as 22q11.2 deletion syndrome (22q11DS), are congenital-anomaly disorders caused by a de novo hemizygous 22q11.2 deletion mediated by meiotic nonallelic homologous recombination events between...
5.
The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans
Ripoll Vera T, Iglesias L, Hermida Prieto M, Ortiz M, Rodriguez Garcia I, Govea Callizo N, et al.
Int J Cardiol . 2010 Jun; 145(2):405-407. PMID: 20542340
Background: The R820W mutation in the MYBPC3 gene has been associated with the development of hypertrophic cardiomyopathy (HCM) in rag-doll cats, but had not been described in humans. Aims: To...