Ariel Brautbar

Ariel Brautbar

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Ariel Brautbar

Ariel Brautbar

Publications by authors named "Ariel Brautbar"

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38Publications

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Severe hypercholesterolemia and liver disease in a 3-year old.

J Clin Lipidol 2016 May-Jun;10(3):650-3. Epub 2015 Dec 23.

Pediatric Endocrinology and Diabetes, Cook Children's Medical Center, Fort Worth, TX.

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https://linkinghub.elsevier.com/retrieve/pii/S19332874153000
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http://dx.doi.org/10.1016/j.jacl.2015.12.020DOI Listing
October 2017

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

J Cardiovasc Pharmacol 2015 Aug;66(2):183-8

*Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI; †Health Services Research and Development, Michael E. DeBakey Veterans Affairs Medical Center and Section of Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, TX; and ‡Division of Genetics and Endocrinology, Cook Children's Medical Center, Fort Worth, TX.

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http://dx.doi.org/10.1097/FJC.0000000000000261DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4993018PMC
August 2015

Genetics of familial hypercholesterolemia.

Curr Atheroscler Rep 2015 Apr;17(4):491

Division of Genetics, Cook Children's Medical Center, Fort Worth, TX, USA,

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http://dx.doi.org/10.1007/s11883-015-0491-zDOI Listing
April 2015

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

Atherosclerosis 2014 Jun 22;234(2):249-53. Epub 2014 Mar 22.

Section of Cardiovascular Research, Baylor College of Medicine, Houston, TX, USA; Center for Cardiovascular Disease Prevention, Methodist DeBakey Heart and Vascular Center, Houston, TX, USA; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI, USA. Electronic address:

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http://dx.doi.org/10.1016/j.atherosclerosis.2014.03.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4078400PMC
June 2014

Single nucleotide polymorphisms in cholesteryl ester transfer protein gene and recurrent coronary heart disease or mortality in patients with established atherosclerosis.

Am J Cardiol 2013 Nov 25;112(9):1287-92. Epub 2013 Jul 25.

Health Services Research and Development Center of Excellence, Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas; Section of Cardiovascular Research, Department of Internal Medicine, Baylor College of Medicine, Houston, Texas. Electronic address:

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http://dx.doi.org/10.1016/j.amjcard.2013.05.073DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3800478PMC
November 2013

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

J Clin Lipidol 2013 Jan-Feb;7(1):82-7. Epub 2012 Sep 29.

Center for Atherosclerosis and Lipoprotein Research, Baylor College of Medicine, Houston, TX 77030, USA.

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http://dx.doi.org/10.1016/j.jacl.2012.09.004DOI Listing
August 2013

Interaction between SNPs in the RXRA and near ANGPTL3 gene region inhibits apoB reduction after statin-fenofibric acid therapy in individuals with mixed dyslipidemia.

J Lipid Res 2012 Nov 15;53(11):2425-8. Epub 2012 Aug 15.

Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, USA.

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http://dx.doi.org/10.1194/jlr.M028829DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466010PMC
November 2012

Knowledge-driven analysis identifies a gene-gene interaction affecting high-density lipoprotein cholesterol levels in multi-ethnic populations.

PLoS Genet 2012 24;8(5):e1002714. Epub 2012 May 24.

Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, New York, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1002714DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3359971PMC
September 2012

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.

Atherosclerosis 2012 May 3;222(1):135-7. Epub 2012 Feb 3.

Section of Atherosclerosis and Vascular Medicine, Department of Medicine, Baylor College of Medicine, Methodist DeBakey Heart and Vascular Center, the Methodist Hospital, Houston, TX, USA.

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http://dx.doi.org/10.1016/j.atherosclerosis.2012.01.028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334435PMC
May 2012

Necrotizing soft tissue infection: an unusual and devastating complication of pressure sores.

Isr Med Assoc J 2011 Jul;13(7):442-3

Department of Internal Medicine, Shaare Zedek Medical Center, affiliated with Hebrew University-Hadassah Medical School, Jerusalem, Israel.

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July 2011

Pharmacological strategies for lowering LDL cholesterol: statins and beyond.

Nat Rev Cardiol 2011 May 15;8(5):253-65. Epub 2011 Feb 15.

Section of Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Methodist DeBakey Heart and Vascular Center, 6565 Fannin, M.S. A-601, Houston, TX 77030, USA.

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http://dx.doi.org/10.1038/nrcardio.2011.2DOI Listing
May 2011

FBN1 mutations in patients with descending thoracic aortic dissections.

Am J Med Genet A 2010 Feb;152A(2):413-6

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas 77030, USA.

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http://doi.wiley.com/10.1002/ajmg.a.32856
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http://dx.doi.org/10.1002/ajmg.a.32856DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593235PMC
February 2010

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

Am J Med Genet A 2009 Mar;149A(3):559-62

Department of Molecular and Human Genetics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas 77030, USA.

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http://dx.doi.org/10.1002/ajmg.a.32671DOI Listing
March 2009

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

Mol Genet Metab 2009 Feb 4;96(2):59-65. Epub 2008 Dec 4.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, NAB 2015, Houston, TX 77030, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S109671920800256
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http://dx.doi.org/10.1016/j.ymgme.2008.10.006DOI Listing
February 2009

Gaucher disease in Arab patients at an Israeli referral clinic.

Isr Med Assoc J 2008 Aug-Sep;10(8-9):600-2

Gaucher Clinic, Shaare Zedek Medical Center, Jerusalem, Israel.

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November 2008

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

Mol Genet Metab 2008 Aug 20;94(4):485-90. Epub 2008 May 20.

Department of Molecular and Human Genetics, Baylor College of Medicine, One Baylor Plaza, NAB 2015, Houston, TX 77030, USA.

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http://dx.doi.org/10.1016/j.ymgme.2008.04.004DOI Listing
August 2008

Spontaneous bacterial peritonitis caused by Haemophilus parainfluenzae.

Isr Med Assoc J 2007 Mar;9(3):175-6

Department of Internal Medicine, Shaare Zedek Medical Center, Jerusalem, Israel.

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March 2007

Effect of enzyme replacement therapy on gammopathies in Gaucher disease.

Blood Cells Mol Dis 2004 Jan-Feb;32(1):214-7

Gaucher Clinic, Shaare Zedek Medical Center, Jerusalem 91031, Israel.

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September 2004

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

Blood Cells Mol Dis 2003 Sep-Oct;31(2):187-9; discussion 190-1

Department of Medicine, Shaare Zedek Medical Center, Jerusalem 91031, Israel.

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May 2004