I. López Pajares - Concepedia

Author

I. López Pajares

Also Known As

I Lopez Pajares, I López Pajares, I PAJARES, I. Lopez Pajares, I. López Pajares, I.L. Pajares, I.Lopez Pajares, Isidora Lopez Pajares, Isidora López Pajares

Publications

906

Citations

H-Index

Concepts

All Affiliations

Hospital Universitario La Paz Centre for Biomedical Network Research on Rare Diseases Hospital Universitario Son Dureta Instituto de Investigación de Enfermedades Raras Medical Genetics Center

About

I. López Pajares is an author at Hospital Universitario La Paz specializing in medicine, genetics, and chromosome 9.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	234
2	Health Sciences	2	2	42
3	Natural Sciences	1	1	13
4	Public Health	1	1	11
5	Molecular Biology	1	1	13

I. López Pajares

Publications

732

Citations

H-Index

Page 1

	Year	Citations
Mapping translocation breakpoints by next-generation sequencing Wei Chen, Vera M. Kalscheuer, Andreas Tzschach, Genome Research	2008	138
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism Georgia Karadima, Merete Bugge, Peter Nicolaidis, European Journal of Human Genetics Developmental BiologyCytogeneticsGenetic DisorderGeneticsTrisomy 8	1998	131
Comparative study of three diagnostic approaches (FISH, STRs and MLPA) in 30 patients with 22q11.2 deletion syndrome Luís Fernández, Pablo Lapunzina, Dolores Arjona, Clinical Genetics	2005	90
Euchromatic variant 16p+. Implications in prenatal diagnosis I. López Pajares, Olaya Villa, Marta Salido, Prenatal Diagnosis	2006	77
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review Luís Fernández, Julián Nevado, Fernando Santos, BMC Medical Genetics	2009	68
MLPA <i>vs</i> multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation Alicia Delicado, Pablo Lapunzina, Dolores Arjona, Clinical Genetics	2006	32
Higher frequency of uncommon 1.5–2 Mb deletions found in familial cases of 22q11.2 deletion syndrome Luís Fernández, Pablo Lapunzina, I. López Pajares, American Journal of Medical Genetics Part A	2005	27
A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36). Alicia Delicado, E Escribano, I. López Pajares, Journal of Medical Genetics CytogeneticsGeneticsGynecologyMolecular GeneticsCongenital Heart Anomaly	1991	26
Hyperekplexia (Startle Disease) Pablo Lapunzina, Juan Martínez Sánchez, Marta Cabrera, Molecular Diagnosis Startle DiseaseGenetic DisorderPathogenesisHistopathologyDiagnosis	2003	24
Trisomy 20p from maternal translocation and anencephaly. Case report and genetic review. R. M. Zumel, M. Teresa Darnaude, Alicia Delicado, PubMed	1989	24

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