Brautbar, Ariel: search on Z-Library

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1

FBN1 mutations in patients with descending thoracic aortic dissections

Ariel Brautbar, Scott A. LeMaire, Luis M. Franco, Joseph S. Coselli, Dianna M. Milewicz, John W. Belmont

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 82 KB

english, 2010

2

198-P: HLA immunogenetics of multiple sclerosis in Israeli arabs

Gil Benedek, Tamar Paperna, Nili Avidan, Izabella Lejbkowicz, Jorge Oksenberg, Chaim Brautbar, Shoshana Israel, Ariel Miller

Journal:

Human Immunology

Year:

2009

Language:

english

File:

PDF, 42 KB

english, 2009

3

Single Nucleotide Polymorphisms in Cholesteryl Ester Transfer Protein Gene and Recurrent Coronary Heart Disease or Mortality in Patients With Established Atherosclerosis

Virani, Salim S., Lee, Vei-Vei, Brautbar, Ariel, Grove, Megan L., Nambi, Vijay, Alam, Mahboob, Elayda, MacArthur, Wilson, James M., Willerson, James T., Boerwinkle, Eric, Ballantyne, Christie M.

Journal:

The American Journal of Cardiology

Year:

2013

Language:

english

File:

PDF, 139 KB

english, 2013

4

SINGLE NUCLEOTIDE POLYMORPHISMS IN CHOLESTERYL ESTER TRANSFER PROTEIN (CETP) GENE ARE NOT ASSOCIATED WITH RECURRENT CARDIOVASCULAR EVENTS OR MORTALITY IN PATIENTS WITH ESTABLISHED ATHEROSCLEROSIS: A MENDELIAN RANDOMIZATION EXPERIMENT

Virani, Salim S., Lee, Vei-Vei, Brautbar, Ariel, Gove-Goana, Megan, Nambi, Vijay, Alam, Mahboob, Elayda, MacArthur, Wilson, James, Willerson, James, Boerwinkle, Eric, Ballantyne, Christie, DeBakey, Mi

Journal:

Journal of the American College of Cardiology

Year:

2013

Language:

english

File:

PDF, 150 KB

english, 2013

5

Severe hypercholesterolemia and liver disease in a 3-year old

Patel, Amol M., Brautbar, Ariel, Desai, Nirav K., Wilson, Don P.

Journal:

Journal of Clinical Lipidology

Year:

2016

Language:

english

File:

PDF, 844 KB

english, 2016

6

ASSOCIATIONS BETWEEN A SINGLE NUCLEOTIDE POLYMORPHISM IN CHROMOSOME 9P21 AND ARTERIAL STIFFNESS IN THE ATHEROSCLEROSIS RISK IN COMMUNITIES STUDY

Nambi, Vijay, Pompeii, Lisa, Sharrett, Richey, Yang, Eric, Brautbar, Ariel, Franceschini, Nora, North, Kari, Coresh, Josef, Virani, Salim, Ballantyne, Christie, Boerwinkle, Eric

Journal:

Journal of the American College of Cardiology

Year:

2011

Language:

english

File:

PDF, 242 KB

english, 2011

7

Combined 21- and llß-Hydroxylase Deficiency in Familial Congenital Adrenal Hyperplasia*

HURWITZ, ARYE, BRAUTBAR, CHAIM, MILWIDSKY, ARIEL, VECSEI, PAUL, MILEWICZ, ANDRE, NAVOT, DANIEL, RÖSLER, ARIEL

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

1985

Language:

english

File:

PDF, 1.16 MB

english, 1985

8

The Prevalence of Dyslipidemia and Other Cardiovascular Risk Factors in Youth with Diabetes

Vinson, Amelia, Wilson, Don P., O'Reilly, Crystal M., Gonzalez, Jose, de la Torre, Alejandro, Brautbar, Ariel

Journal:

Journal of Clinical Lipidology

Year:

2015

Language:

english

File:

PDF, 42 KB

english, 2015

9

Genetics of Familial Hypercholesterolemia

Brautbar, Ariel, Leary, Emili, Rasmussen, Kristen, Wilson, Don P., Steiner, Robert D., Virani, Salim

Journal:

Current Atherosclerosis Reports

Year:

2015

Language:

english

File:

PDF, 1.21 MB

english, 2015

10

A 3-Year-Old with Severe Hypercholesterolemia*

Patel, Amol M., Wilson, Don P., de la Torre, Alejandro, Brautbar, Ariel

Journal:

Journal of Clinical Lipidology

Year:

2015

Language:

english

File:

PDF, 408 KB

english, 2015

11

Genetic Mutation of the LDL-C Receptor without Hypercholesterolemia

Jarvis, Todd, Brautbar, Ariel, Hamilton, Luke, Ahmad, Zahid, Wilson, Don

Journal:

Journal of Clinical Lipidology

Year:

2017

Language:

english

File:

PDF, 212 KB

english, 2017

12

Two mtDNA mutations 14487T>C (M63V, ND6) and 12297T>C (tRNA Leu) in a Leigh syndrome family

Jing Wang, Ariel Brautbar, Alicia K. Chan, Tara Dzwiniel, Fang-yuan Li, Paula J. Waters, Brett H. Graham, Lee-Jun Wong

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 553 KB

english, 2009

13

The 9p21 genetic variant is additive to carotid intima media thickness and plaque in improving coronary heart disease risk prediction in white participants of the Atherosclerosis Risk in Communities (ARIC) Study

Vijay Nambi, Eric Boerwinkle, Kim Lawson, Ariel Brautbar, Lloyd Chambless, Nora Franeschini, Kari E. North, Salim S. Virani, Aaron R. Folsom, Christie M. Ballantyne

Journal:

Atherosclerosis

Year:

2012

Language:

english

File:

PDF, 162 KB

english, 2012

14

011–Lipid Screening in Youth

Vinson, Amelia, Guerra, Lisa R., Hamilton, Luke, Williams, Lauren, Murphy, Ryan, de la Torre, Alejandro, Wilson, Don P., Brautbar, Ariel

Journal:

Journal of Pediatric Nursing

Year:

2017

Language:

english

File:

PDF, 53 KB

english, 2017

15

Usefulness of Single Nucleotide Polymorphism in Chromosome 4q25 to Predict In-Hospital and Long-Term Development of Atrial Fibrillation and Survival in Patients Undergoing Coronary Artery Bypass Grafting

Salim S. Virani, Ariel Brautbar, Vei-Vei Lee, MacArthur Elayda, Shehzad Sami, Vijay Nambi, Lorraine Frazier, James M. Wilson, James T. Willerson, Eric Boerwinkle, Christie M. Ballantyne

Journal:

The American Journal of Cardiology

Year:

2011

Language:

english

File:

PDF, 172 KB

english, 2011

16

Menetrier??s disease presenting as an acute protein-losing gastroenteropathy in a 27-year-old man with Gaucher disease

Brautbar, Ariel, Paz, Julian, Hadas-Halpern, Irith, Reinus, Constantin, Rosenmann, Eliezer, Zimran, Ari, Elstein, Deborah

Journal:

European Journal of Gastroenterology & Hepatology

Year:

2005

Language:

english

File:

PDF, 107 KB

english, 2005

17

Knowledge-Driven Analysis Identifies a Gene–Gene Interaction Affecting High-Density Lipoprotein Cholesterol Levels in Multi-Ethnic Populations

Ma, Li, Brautbar, Ariel, Boerwinkle, Eric, Sing, Charles F., Clark, Andrew G., Keinan, Alon, Williams, Scott M.

Journal:

Year:

2012

Language:

english

File:

PDF, 415 KB

english, 2012

18

Variants in the APOA5 gene region and the response to combination therapy with statins and fenofibric acid in a randomized clinical trial of individuals with mixed dyslipidemia

Ariel Brautbar, Daniel Covarrubias, John Belmont, Fremiet Lara-Garduno, Salim S. Virani, Peter H. Jones, Suzanne M. Leal, Christie M. Ballantyne

Journal:

Atherosclerosis

Year:

2011

Language:

english

File:

PDF, 125 KB

english, 2011

19

Pharmacological strategies for lowering LDL cholesterol: statins and beyond

Brautbar, Ariel, Ballantyne, Christie M.

Journal:

Nature Reviews Cardiology (formerly Nature Clinical Practice Cardiovascular Medicine)

Year:

2011

Language:

english

File:

PDF, 884 KB

english, 2011

20

A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease

Negi, Smita I., Brautbar, Ariel, Virani, Salim S., Anand, Aashish, Polisecki, Eliana, Asztalos, Bela F., Ballantyne, Christie M., Schaefer, Ernst J., Jones, Peter H.

Journal:

Journal of Clinical Lipidology

Year:

2013

Language:

english

File:

PDF, 701 KB

english, 2013

21

Chromosome 9p21 Single Nucleotide Polymorphisms Are Not Associated With Recurrent Myocardial Infarction in Patients With Established Coronary Artery Disease

Virani, Salim S., Brautbar, Ariel, Lee, Vei-Vei, Elayda, MacArthur, Morrison, Alanna C., Grove, Megan L., Nambi, Vijay, Frazier, Lorraine, Wilson, James M., Willerson, James T., Boerwinkle, Eric, Ball

Journal:

Circulation Journal

Year:

2012

Language:

english

File:

PDF, 518 KB

english, 2012

22

Analysis of Multiple Association Studies Provides Evidence of an Expression QTL Hub in Gene-Gene Interaction Network Affecting HDL Cholesterol Levels

Ma, Li, Ballantyne, Christie, Brautbar, Ariel, Keinan, Alon, Yu, Zhaoxia

Journal:

Year:

2014

Language:

english

File:

PDF, 454 KB

english, 2014

23

Differential Lipid Response to Statins Is Associated With Variants in the BUD13–APOA5 Gene Region

OʼBrien, Sarah E., Schrodi, Steven J., Ye, Zhan, Brilliant, Murray H., Virani, Salim S., Brautbar, Ariel

Journal:

Journal of Cardiovascular Pharmacology

Year:

2015

Language:

english

File:

PDF, 307 KB

english, 2015

24

HLA in a Selective Aldosterone Biosynthetic Defect due to Type 2 Corticosterone Methyl-Oxidase Deficiency

Chaim Brautbar, Rachel Theodor, Joseph Sack, Cyril Levene, Bo Dupont, Lenore S. Levine, Raphael Sharon, Shoshana Smaller, Tirza Cohen, Ariel Rösler

Journal:

Tissue Antigens

Year:

1981

Language:

english

File:

PDF, 243 KB

english, 1981

25

Effect of enzyme replacement therapy on gammopathies in Gaucher disease

Ariel Brautbar, Deborah Elstein, Guy Pines, Aya Abrahamov, Ari Zimran

Journal:

Blood Cells, Molecules, and Diseases

Year:

2004

Language:

english

File:

PDF, 91 KB

english, 2004

26

A genetic risk score based on direct associations with coronary heart disease improves coronary heart disease risk prediction in the Atherosclerosis Risk in Communities (ARIC), but not in the Rotterdam and Framingham Offspring, Studies

Ariel Brautbar, Lisa A. Pompeii, Abbas Dehghan, Julius S. Ngwa, Vijay Nambi, Salim S. Virani, Fernando Rivadeneira, André G. Uitterlinden, Albert Hofman, Jacqueline C.M. Witteman, Michael J. Pencina,

Journal:

Atherosclerosis

Year:

2012

Language:

english

File:

PDF, 157 KB

english, 2012

27

Screening for genetic mutations in children and adolescents with dyslipidemia: importance of early identification and implications of missed diagnoses

Wilson, Don P., de la Torre, Alejandro, Brautbar, Ariel, Hamilton, Luke

Journal:

Expert Opinion on Orphan Drugs

Year:

2016

Language:

english

File:

PDF, 1.10 MB

english, 2016

28

Is this the Coffin–Siris syndrome or the BOD syndrome?

Ariel Brautbar, Judith Ragsdale, Marwan Shinawi

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 110 KB

english, 2009

29

Rare LPL gene variants attenuate triglyceride reduction and HDL cholesterol increase in response to fenofibric acid therapy in individuals with mixed dyslipidemia

Gao, Feng, Ballantyne, Christie, Ma, Li, Virani, Salim S., Keinan, Alon, Brautbar, Ariel

Journal:

Atherosclerosis

Year:

2014

Language:

english

File:

PDF, 210 KB

english, 2014

30

The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle

Ariel Brautbar, Jing Wang, Jose E. Abdenur, Richard C. Chang, Janet A. Thomas, Theresa A. Grebe, Cynthia Lim, Shao-Wen Weng, Brett H. Graham, Lee-Jun Wong

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 340 KB

english, 2008

31

The 1604A (R496H) mutation in Gaucher disease: genotype/phenotype correlation

Ariel Brautbar, Deborah Elstein, Aya Abrahamov, Marsha Zeigler, Gaya Chicco, Ernest Beutler, C.Ronald Scott, Ari Zimran

Journal:

Blood Cells, Molecules, and Diseases

Year:

2003

Language:

english

File:

PDF, 52 KB

english, 2003

32

THE 9P21 GENETIC VARIANT IS ADDITIVE TO CAROTID INTIMA MEDIA THICKNESS AND PLAQUE IN IMPROVING CORONARY HEART DISEASE RISK PREDICTION IN WHITE PARTICIPANTS OF THE ATHEROSCLEROSIS RISK IN COMMUNITIES (ARIC) STUDY

Nambi, Vijay, Boerwinkle, Eic, Lawson, Kim, Brautbar, Ariel, Chambless, Lloyd, Franchescini, Nora, North, Kari, Virani, Salim, Folsom, Aaron R.

Journal:

Journal of the American College of Cardiology

Year:

2010

Language:

english

File:

PDF, 76 KB

english, 2010

33

SINGLE NUCLEOTIDE POLYMORPHISMS IN CHROMOSOME 4Q25 PREDICT IN-HOSPITAL AND LONG TERM DEVELOPMENT OF ATRIAL FIBRILLATION AND SURVIVAL IN PATIENTS UNDERGOING CORONARY ARTERY BYPASS GRAFTING

Virani, Salim S., Brautbar, Ariel, Lee, Vei-Vei, Elayda, MacArthur, Sami, Shehzad, Nambi, Vijay, Frazier, Lorraine, Wilson, James M., Willerson, James T., Boerwinkle, Eric, Ballantyne, Christie M.

Journal:

Journal of the American College of Cardiology

Year:

2011

Language:

english

File:

PDF, 239 KB

english, 2011

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