Concepedia

Author

Javier Sánchez

Hospital Universitario Virgen del RocíoORCID

Also Known As

J M Sanchez, J M Sánchez, J Macías Sánchez, J Sánchez, J. Sanchez, J. Sánchez, J.M. Sánchez, JOSÉ MARTÍN RODRÍGUEZ SÁNCHEZ, Javier Sanchez, Javier Sánchez

43

Publications

481

Citations

11

H-Index

43

Concepts

All Affiliations

Hospital Universitario Virgen del RocíoUniversidad Autónoma de Madrid
JS

About

Javier Sánchez is an author at Hospital Universitario Virgen del Rocío specializing in medicine, developmental biology, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

216

2

Health Sciences

1

1

14

3

Natural Sciences

1

1

24

4

Biology

1

1

24

5

Cell Biology

1

1

14

Javier Sánchez

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9

Publications

392

Citations

9

H-Index

YearCitations

Hepatitis C virus antibodies and liver disease in patients with porphyria cutanea tarda

Mar Decastro, Javier Sánchez, Jesús Fernández Herrera,

Hepatology

1993

152

Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy

José Cervera, Pau Montesinos, José‐Ángel Hernández‐Rivas,

Haematologica

2009

87

A case of deletion 2q35----qter and a peculiar phenotype.

Javier Sánchez, A M Pantano

Journal of Medical Genetics

1984

39

Prenatal diagnosis of 13q– syndrome in a fetus with holoprosencephaly and thumb agenesis

Juan M. Gutiérrez, Waldo Sepúlveda, Rafael Salván Saez,

Ultrasound in Obstetrics and Gynecology

2001

26

Somatic mosaicism for Y120X mutation in the MECP2 gene causes atypical Rett syndrome in a male

Juan I. Pieras, Beatriz Muñoz Cabello, Salud Borrego,

Brain and Development

2010

26

Effects of the space environment on Drosophila melanogaster development. Implications of the IML-2 experiment

Roberto de Marco, Alberto Benguría, Javier Sánchez,

Journal of Biotechnology

1996

24

Loss of Chromosomal Integrity in Neoplasia

Thea D. Tlsty, Piotr Jonczyk, Anne White,

Cold Spring Harbor Symposia on Quantitative Biology

1993

14

Interstitial 10p deletion derived from a maternal ins(16;10)(q22;p13p15.2): Report of the first familial case of 10p monosomy affecting to two familial members of different generations

Raquel M. Fernández, Javier Sánchez, Lutgardo García‐Díaz,

American Journal of Medical Genetics Part A

2016

13

Reverse mutation in fragile X syndrome.

Guillermo Antiñolo, Salud Borrego, Juan C. Cabeza,

PubMed

1996

11

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