Arturo Anguiano - Concepedia

Author

Arturo Anguiano

Quest Diagnostics (United States)

Also Known As

A Anguiano, A. Anguiano, Anguiano, Arturo, Arturo Anguiano, Arturo L Anguiano, Arturo L. Anguiano

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Quest Diagnostics (United States)Center for Human Genetics Rady Children's Hospital-San Diego Boston University

About

Arturo Anguiano is an author at Quest Diagnostics (United States) specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	620
2	Natural Sciences	2	2	68
3	Public Health	2	2	449
4	Health Sciences	1	1	17
5	Anatomy	1	1	371

Arturo Anguiano

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Congenital Bilateral Absence of the Vas Deferens Arturo Anguiano JAMA GeneticsGenetic EpidemiologyVascular MalformationTopographical AnatomyPathology	1992	371
Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis. Arturo Anguiano, Robert D. Oates, Michael Dean, PubMed	1992	134
Twin brothers with MIDAS syndrome and XX karyotype Arturo Anguiano, Xiaojing Yang, J.K. Felix, American Journal of Medical Genetics Part A	2002	100
Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory Boris T Wang, Thomas P Chong, Fatih Z Boyar, Molecular Cytogenetics	2014	91
Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility Jia‐Chi Wang, Leslie Ross, Loretta W Mahon, European Journal of Human Genetics Genetic AnalysisAllelic VariantClinical UtilityGeneticsMedicine	2014	78
Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin Felicitas Lacbawan, Beverly J. White, Arturo Anguiano, American Journal of Medical Genetics CytogeneticsGeneticsGynecologyPaternal OriginRare Interstitial Deletion	1999	55
Fluorescence In Situ Hybridization and K-ras Analyses Improve Diagnostic Yield of Endoscopic Ultrasound-Guided Fine-Needle Aspiration of Solid Pancreatic Masses Sofiya Reicher, Fatih Z Boyar, Maher Albitar, Pancreas	2011	45
Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD Jessica Vasale, Fatih Z Boyar, Michael Jocson, Neuromuscular Disorders Natural SciencesSpectroscopySouthern BlotMolecular BiologyMolecular Combing	2015	41
A large deletion in the CFTR gene in CBAVD Feras Hantash, Aubrey Milunsky, Zhenyuan Wang, Genetics in Medicine GeneticsProtein GeneticsGene StructureGene CharacterizationMolecular Genetics	2006	30
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotype Weimin Sun, Ben Anderson, Joy B. Redman, Genetics in Medicine Allelic VariantMendelian DisorderCftr 5TGenetic DisorderGenetics	2006	30

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