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An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

Science (American Association for the Advancement of Science), 2012-07, Vol.337 (6090), p.100-104

2012

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Phenome-wide association study using research participants' self-reported data provides insight into the Th17 and IL-17 pathway

PloS one, 2017-11, Vol.12 (11), p.e0186405-e0186405

2017

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Performance of genotype imputation for rare variants identified in exons and flanking regions of genes

PloS one, 2011-09, Vol.6 (9), p.e24945-e24945

2011

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Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes

Human molecular genetics, 2018-08, Vol.27 (15), p.2762-2772

2018

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Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib

PloS one, 2017-07, Vol.12 (7), p.e0182115-e0182115

2017

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High-resolution HLA genotyping and severe cutaneous adverse reactions in lamotrigine-treated patients

Pharmacogenetics and genomics, 2009-09, Vol.19 (9), p.661-665

2009

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Assessment of diabetes-related distress

Diabetes care, 1995-06, Vol.18 (6), p.754-760

1995

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Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

Diabetes (New York, N.Y.), 2012-05, Vol.61 (5), p.1297-1301

2012

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Stable association of chloroplastic precursors with protein translocation complexes that contain proteins from both envelope membranes and a stromal Hsp100 molecular chaperone

The EMBO journal, 1997-03, Vol.16 (5), p.935-946

1997

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The Evolutionary Origin of the Protein-Translocating Channel of Chloroplastic Envelope Membranes: Identification of a Cyanobacterial Homolog

Proceedings of the National Academy of Sciences - PNAS, 1999-01, Vol.96 (2), p.784-789

1999

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Insulin omission in women with IDDM

Diabetes care, 1994-10, Vol.17 (10), p.1178-1185

1994

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Validación observacional de la teoría del aprendizaje pedagógico de Juan Enrique Azcoaga con ratones CD1

Revista científica (Universidad del Zulia. Facultad de Ciencias Veterinarias. División de Investigación), 2022-03, Vol.XXXII (single), p.1-15

2022

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Point Mutations in the Murine Fumarylacetoacetate Hydrolase Gene: Animal Models for the Human Genetic Disorder Hereditary Tyrosinemia Type 1

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.641-645

2001

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MO802: Genetics Plays a Limited Role in ESA-Hyporesponsiveness and Haemoglobin Outcomes in End-Stage Renal Disease Patients on Haemodialysis

Nephrology, dialysis, transplantation, 2022-05, Vol.37 (Supplement_3)

2022

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Two chloroplastic protein translocation components, Tic110 and Toc75, are conserved in different plastid types from multiple plant species

Plant molecular biology, 2003-01, Vol.51 (2), p.175-181

2003

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High-resolution HLA genotyping and severe cutaneous adverse reactions in lamotrigine-treated patients

Pharmacogenetics and genomics, 2009-09, Vol.19 (9), p.661-665

2009

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MP20-13 STENT COLONIZATION: DISCORDANCE WITH URINE CULTURE

The Journal of urology, 2015-04, Vol.193 (4), p.e228-e228

2015

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Evaluation of novel derivatisation reagents for the analysis of oxysterols

Biochemical and biophysical research communications, 2014-04, Vol.446 (3), p.756-761

2014

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The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease in Two Large Populations

American journal of respiratory and critical care medicine, 2007-07, Vol.176 (2), p.167-173

2007

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Towards the total synthesis of gelsemine

Aponte, Jennifer

2014

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1485 COMPARISON OF SINGLE-CONSOLE VERSUS DUAL-CONSOLE ROBOTIC SURGERY SKILL PERFORMANCE IN UROLOGY RESIDENTS

The Journal of urology, 2011-04, Vol.185 (4), p.e595-e595

2011

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Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe

Human mutation, 2012-07, Vol.33 (7), p.1087-1098

2012

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Absence of association of asporin polymorphisms and osteoarthritis susceptibility in US Caucasians

Osteoarthritis and cartilage, 2008-10, Vol.16 (10), p.1174-1177

2008

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Validación observacional de la teoría del aprendizaje pedagógico de Juan Enrique Azcoaga con ratones CD1

Revista científica (Universidad del Zulia. Facultad de Ciencias Veterinarias. División de Investigación), 2022-03, Vol.32

2022

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1271 A MULTI-INSTITUTIONAL ANALYSIS OF THE ASSOCIATION OF NEPHROMETRY SCORE WITH ISCHEMIA TIME DURING PARTIAL NEPHRECTOMY

The Journal of urology, 2011-04, Vol.185 (4), p.e508-e509

2011

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An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People

Phenome-wide association study using research participants' self-reported data provides insight into the Th17 and IL-17 pathway

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes

Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes

Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib

High-resolution HLA genotyping and severe cutaneous adverse reactions in lamotrigine-treated patients

Assessment of diabetes-related distress

Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation

Stable association of chloroplastic precursors with protein translocation complexes that contain proteins from both envelope membranes and a stromal Hsp100 molecular chaperone

The Evolutionary Origin of the Protein-Translocating Channel of Chloroplastic Envelope Membranes: Identification of a Cyanobacterial Homolog

Insulin omission in women with IDDM

Validación observacional de la teoría del aprendizaje pedagógico de Juan Enrique Azcoaga con ratones CD1

Point Mutations in the Murine Fumarylacetoacetate Hydrolase Gene: Animal Models for the Human Genetic Disorder Hereditary Tyrosinemia Type 1

MO802: Genetics Plays a Limited Role in ESA-Hyporesponsiveness and Haemoglobin Outcomes in End-Stage Renal Disease Patients on Haemodialysis

Two chloroplastic protein translocation components, Tic110 and Toc75, are conserved in different plastid types from multiple plant species

High-resolution HLA genotyping and severe cutaneous adverse reactions in lamotrigine-treated patients

MP20-13 STENT COLONIZATION: DISCORDANCE WITH URINE CULTURE

Evaluation of novel derivatisation reagents for the analysis of oxysterols

The SERPINE2 Gene Is Associated with Chronic Obstructive Pulmonary Disease in Two Large Populations

Towards the total synthesis of gelsemine

1485 COMPARISON OF SINGLE-CONSOLE VERSUS DUAL-CONSOLE ROBOTIC SURGERY SKILL PERFORMANCE IN UROLOGY RESIDENTS

Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe

Absence of association of asporin polymorphisms and osteoarthritis susceptibility in US Caucasians

Validación observacional de la teoría del aprendizaje pedagógico de Juan Enrique Azcoaga con ratones CD1

1271 A MULTI-INSTITUTIONAL ANALYSIS OF THE ASSOCIATION OF NEPHROMETRY SCORE WITH ISCHEMIA TIME DURING PARTIAL NEPHRECTOMY

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