Concepedia

Author

F Ballesta

Hospital Clínic de Barcelona

Also Known As

F Ballesta, F. Ballesta, Francesca Ballesta

40

Publications

744

Citations

15

H-Index

46

Concepts

All Affiliations

Hospital Clínic de BarcelonaUniversitat de BarcelonaDuran i Reynals HospitalConsorci Institut D'Investigacions Biomediques August Pi I SunyerUniversitat Autònoma de Barcelona
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About

F Ballesta is an author at Hospital Clínic de Barcelona specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

9

9

335

2

Molecular Genetics

6

6

196

3

Public Health

2

2

132

4

Molecular Biology

2

2

121

5

Nephrology

1

1

22

F Ballesta

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17

Publications

713

Citations

15

H-Index

YearCitations

Molecular, cytogenetic, and clinical characterisation of six XX males including one prenatal diagnosis.

Ester Margarit, Anna Soler, Ana Carrió,

Journal of Medical Genetics

1998

105

Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.

Judy Fantes, Wendy A. Bickmore, Judy Fletcher,

PubMed

1992

104

Fragile X syndrome and the (CGG)n mutation: two families with discordant MZ twins.

H. Kruyer, Montserrat Milà, G. Glóver,

PubMed

1994

96

Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene

Ester Margarit, Vanessa Bach, David Salas Gomez,

Clinical Genetics

2005

96

A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures

Mario Ezquerra, Rafael Blesa, Josep Lluís Gelpí,

Neurology

1999

49

Dentatorubropallidoluysian atrophy in a Spanish family: a clinical, radiological, pathological, and genetic study

Montserrat Milà, Aurora Sánchez, P. Latorre,

Journal of Neurology Neurosurgery & Psychiatry

1999

42

Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.

F Ballesta, R. Queralt, David Gómez,

PubMed

1999

28

Meiotic and sperm chromosome studies in a reciprocal translocation t(1;2)(q32;q36)

C. Templado, J. Navarro, R. Requena,

Human Genetics

1990

27

Molecular analysis of the (CGG)n expansion in the FMR-1 gene in 59 Spanish fragile X syndrome families

M. De Mil, H. Kruyer, G. Glóver,

Human Genetics

1994

25

Prognostic Significance of Cytogenetical Studies in Chronic Granulocytic Leukaemia

Francisco Cervantes, C Rozmán, F Ballesta,

Scandinavian Journal of Haematology

1982

23

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