Genetic Variants in LRP1 and ULK4 Are Associated with Acute Aortic Dissections

American Journal of Human Genetics

Volumn 99, Issue 3, 2016, Pages 762-769

  Guo, Dong chuan ^a   Grove, Megan L ^b   Prakash, Siddharth K ^a   Eriksson, Per ^c   Hostetler, Ellen M ^a   LeMaire, Scott A ^d   Body, Simon C ^e   Shalhub, Sherene ^f   Estrera, Anthony L ^a   Safi, Hazim J ^a   Regalado, Ellen S ^a   Zhou, Wei ^g   Mathis, Michael R ^g   Eagle, Kim A ^h   Yang, Bo ^h   Willer, Cristen J ^g   Boerwinkle, Eric ^b,i   Milewicz, Dianna M ^a  

^a UNIVERSITY OF TEXAS   (United States)

^b UNIVERSITY OF TEXAS SCHOOL OF PUBLIC HEALTH   (United States)

^c KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^d ST LUKE S EPISCOPAL HOSPITAL   (United States)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

^f UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^g UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^h UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

ⁱ BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FIBRILLIN 1; LOW DENSITY LIPOPROTEIN RECEPTOR RELATED PROTEIN; PHOSPHOTRANSFERASE; UNC 51 LIKE KINASE 4; UNCLASSIFIED DRUG; FBN1 PROTEIN, HUMAN; LRP1 PROTEIN, HUMAN; PROTEIN SERINE THREONINE KINASE; ULK4 PROTEIN, HUMAN;

ACUTE DISEASE; ADULT; AGED; AORTIC DISSECTION; ARTICLE; CONTROLLED STUDY; COPY NUMBER VARIATION; EUROPEAN; FEMALE; GENE DELETION; GENETIC ASSOCIATION; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; THORACIC AORTA; ATHEROSCLEROSIS; CASE CONTROL STUDY; COHORT ANALYSIS; COMPLICATION; DISSECTING ANEURYSM; ETHNOLOGY; EUROPE; EXOME; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETIC VARIATION; GENETICS; HYPERTENSION; MIDDLE AGED; RISK FACTOR; THORACIC AORTA ANEURYSM;

AGED; ANEURYSM, DISSECTING; AORTIC ANEURYSM, THORACIC; ATHEROSCLEROSIS; CASE-CONTROL STUDIES; COHORT STUDIES; DNA COPY NUMBER VARIATIONS; EUROPE; EXOME; FEMALE; FIBRILLIN-1; GENE DELETION; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOTYPE; HUMANS; HYPERTENSION; LINKAGE DISEQUILIBRIUM; LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN-1; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEIN-SERINE-THREONINE KINASES; RISK FACTORS;

EID: 85002620872     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2016.06.034     Document Type: Article

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