L. Arnaud‐López - Concepedia

Author

L. Arnaud‐López

Mexican Social Security Institute

Also Known As

L ARNAUDLOPEZ, L Arnaud‐López, L. Arnaud-López, L. Arnaud‐López, Lisette Arnaud-Lopez, Lisette Arnaud-López

Publications

310

Citations

H-Index

Concepts

All Affiliations

Mexican Social Security Institute Universidad de Guadalajara Hospital de Especialidades

About

L. Arnaud‐López is an author at Mexican Social Security Institute specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	277
2	Public Health	2	2	27
3	Allergy	1	1	136
4	Endocrinology	1	1	136
5	Epidemiology	1	1	16

L. Arnaud‐López

Publications

300

Citations

H-Index

Page 1

	Year	Citations
Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function L. Arnaud‐López, Gianluca Usala, Graziano Ceresini, The American Journal of Human Genetics AllergyThyroid FunctionPhosphodiesterase 8BGenetic DisorderGenetics	2008	136
Crouzon with acanthosis nigricans. Further delineation of the syndrome L. Arnaud‐López, R Fragoso, Johana M. Mantilla-Capacho, Clinical Genetics Developmental AnomalyChiari MalformationMendelian DisorderDisease MechanismClassic Crouzon Syndrome	2007	77
Cytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients Martha Patricia Gallegos‐Arreola, Cecilia M. Batista‐González, José Luis Delgado‐Lamas, Blood Cells Molecules and Diseases Hematological MalignancyMedicineGeneticsCytochrome P4501a1 PolymorphismGenetic Epidemiology	2004	22
Association between the Xba I polymorphism of APOB gene and plasma lipid level in Mexican patients with coronary artery disease. Martha Patricia Gallegos‐Arreola, Yadira Valdez, Marco Zúñiga-Corona, PubMed HypertensionGenetic EpidemiologyHuman PolymorphismHyperlipidemiaVldl Plasma Levels	2012	16
GSTT1 Gene Deletion Is Associated with Lung Cancer in Mexican Patients Martha Patricia Gallegos‐Arreola, Belinda Claudia Gómez‐Meda, Gilberto Morgan‐Villela, Disease Markers Tobacco ControlOncologyGstt1 Gene DeletionMedicineGenetics	2004	15
<i>GATA2</i> null mutation associated with incomplete penetrance in a family with Emberger syndrome Aniel Jessica Leticia Brambila‐Tapia, José Elías García‐Ortíz, Pascal Brouillard, Hematology	2017	13
First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patient Luis E. Becerra-Solano, L. Arnaud‐López, Manuel Díaz-Rodríguez, Clinical Dysmorphology ChromatinChromosomal MosaicismCell DivisionCytogeneticsGenetic Disorder	2008	11
Ambiguous genitalia by 9p deletion inherent to a dic(Y;9)(q12;p24). A.I. Vásquez-Velásquez, L. Arnaud‐López, Luis E. Figuera, PubMed	2005	10

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