Marta Rodríguez de Alba

Author

Hospital Universitario Fundación Jiménez Díaz

Also Known As

Lorena Ondo, M. RODRIGUEZ DE ALBA, M. Rodriguez De Alba, M. Rodriguez de Alba, M. Rodríguez de alba, M. Rodríguez de Alba, MARTA RODRIGUEZ DE ALBA, Marta Rodriguez de Alba, Marta Rodriguez De Alba, Marta Rodriguez de Alba

Publications

1.6K

Citations

H-Index

Concepts

All Affiliations

Hospital Universitario Fundación Jiménez Díaz Centre for Biomedical Network Research on Rare Diseases Universidad Autónoma de Madrid Instituto de Salud Carlos III Universidad Complutense de Madrid

About

Marta Rodríguez de Alba is an author at Hospital Universitario Fundación Jiménez Díaz specializing in medicine, genetics, and obstetrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	338
2	Public Health	6	6	197
3	Molecular Genetics	2	2	29
4	Engineering	1	1	23
5	Molecular Medicine	1	1	13

Marta Rodríguez de Alba

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Prenatal detection of a cystic fibrosis mutation in fetal DNA from maternal plasma María González‐González, M García-Hoyos, M.J. Trujillo, Prenatal Diagnosis	2002	143
MLPA as a screening method of aneuploidy and unbalanced chromosomal rearrangements in spontaneous miscarriages Dan Diego‐Álvarez, Marta Rodríguez de Alba, Rocio Cardero‐Merlo, Prenatal Diagnosis	2007	116
Huntington disease–unaffected fetus diagnosed from maternal plasma using QF‐PCR María González‐González, M.J. Trujillo, Marta Rodríguez de Alba, Prenatal Diagnosis	2003	92
Trisomy 2 due to a 3:1 segregation in an abortion studied by QF‐PCR and CGH Isabel Lorda‐Sánchez, Dan Diego‐Álvarez, Carmen Ayuso, Prenatal Diagnosis	2005	76
Foetal sex determination in maternal blood from the seventh week of gestation and its role in diagnosing haemophilia in the foetuses of female carriers Ana Bustamante‐Aragonés, Marta Rodríguez de Alba, Cristina González-González, Haemophilia	2008	75
New strategy for the prenatal detection/exclusion of paternal cystic fibrosis mutations in maternal plasma Ana Bustamante‐Aragonés, J. Gallego‐Merlo, María José Trujillo-Tiebas, Journal of Cystic Fibrosis Genetic TestingMendelian DisorderPrenatal Genetic TestingMedicineGenetics	2008	59
Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages Dan Diego‐Álvarez, Maria García‐Hoyos, M.J. Trujillo, Human Reproduction	2005	59
Comparison of the diagnostic yield of aCGH and genome-wide sequencing across different neurodevelopmental disorders Francisco Martínez‐Granero, Fiona Blanco‐Kelly, C. Sánchez-Jimeno, npj Genomic Medicine	2021	55
Prenatal diagnosis of Huntington disease in maternal plasma: direct and indirect study Ana Bustamante‐Aragonés, María José Trujillo-Tiebas, J. Gallego‐Merlo, European Journal of Neurology	2008	49
Fetal Genotyping in Maternal Blood by Digital PCR: Towards NIPD of Monogenic Disorders Independently of Parental Origin Sara Perlado, Ana Bustamante‐Aragonés, Marta Donas, PLoS ONE	2016	49

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