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Genome-wide association study of paliperidone efficacy

Pharmacogenetics and genomics, 2017-01, Vol.27 (1), p.7-18

2017

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Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

Genome medicine, 2017-11, Vol.9 (1), p.106-106, Article 106

2017

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A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

Kidney international, 2003-01, Vol.63 (1), p.24-32

2003

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Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

Journal of molecular medicine (Berlin, Germany), 2004-03, Vol.82 (3), p.182-188

2004

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Prospective-–retrospective biomarker analysis for regulatory consideration: white paper from the industry pharmacogenomics working group

Pharmacogenomics, 2011-07, Vol.12 (7), p.939-951

2011

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A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency

The Journal of biological chemistry, 2002-12, Vol.277 (50), p.48610-48616

2002

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Learning from product labels and label changes: how to build pharmacogenomics into drug-development programs

Pharmacogenomics, 2010-12, Vol.11 (12), p.1637-1647

2010

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RETURNING GENETIC RESEARCH RESULTS TO INDIVIDUALS: POINTS-TO-CONSIDER

Bioethics, 2006-02, Vol.20 (1), p.24-36

2006

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Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity Mapping

American journal of human genetics, 1997-12, Vol.61 (6), p.1335-1341

1997

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Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia

Proceedings of the National Academy of Sciences - PNAS, 2002-10, Vol.99 (21), p.13675-13680

2002

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GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

Scientific reports, 2013-10, Vol.3 (1), p.3075-3075, Article 3075

2013

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The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

Nature genetics, 2001-11, Vol.29 (3), p.337-341

2001

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Large-scale candidate gene study to identify genetic risk factors predictive of paliperidone treatment response in patients with schizophrenia

Pharmacogenetics and genomics, 2015-04, Vol.25 (4), p.173-185

2015

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A survey of information literacy credit courses in US academic libraries: Prevalence and characteristics

Reference services review, 2016-01, Vol.44 (4), p.564-582

2016

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SULT4A1 haplotype: conflicting results on its role as a biomarker of antipsychotic response

Pharmacogenomics, 2014-09, Vol.15 (12), p.1557-1564

2014

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Polymorphisms in the multiple drug resistance protein 1 and in P-glycoprotein 1 are associated with time to event outcomes in patients with advanced multiple myeloma treated with bortezomib and pegylated liposomal doxorubicin

Annals of hematology, 2010-11, Vol.89 (11), p.1133-1140

2010

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A survey of information literacy credit courses in US academic libraries

Reference services review, 2016-11, Vol.44 (4), p.564-582

2016

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Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness

Nature genetics, 1999-07, Vol.22 (3), p.300-304

1999

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Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43

American journal of human genetics, 1998-06, Vol.62 (6), p.1416-1424

1998

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Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin

Nature genetics, 2001-10, Vol.29 (2), p.134-136

2001

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Effect of the Cytochrome P450 2C19 Inhibitor Omeprazole on the Pharmacokinetics and Safety Profile of Bortezomib in Patients with Advanced Solid Tumours, Non-Hodgkin’s Lymphoma or Multiple Myeloma

Clinical pharmacokinetics, 2009-01, Vol.48 (3), p.199-209

2009

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PhRMA White Paper on ADME Pharmacogenomics

Journal of clinical pharmacology, 2008-07, Vol.48 (7), p.849-889

2008

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Bilateral Dacryoadenitis: Don’t Forget Tuberculosis

The Pediatric infectious disease journal, 2017-01, Vol.36 (1), p.117-119

2017

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The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter

Nature genetics, 1999-07, Vol.22 (3), p.305-308

1999

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Urgent care centers and virtual visits help avoid unnecessary trips to the ER

Westchester County Business Journal, 2019-05, Vol.55 (19), p.19-19

Cohen, Nadine

2019

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Genome-wide association study of paliperidone efficacy

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients

Prospective-–retrospective biomarker analysis for regulatory consideration: white paper from the industry pharmacogenomics working group

A Novel Mutation (T65P) in the PAS Domain of the Human Potassium Channel HERG Results in the Long QT Syndrome by Trafficking Deficiency

Learning from product labels and label changes: how to build pharmacogenomics into drug-development programs

RETURNING GENETIC RESEARCH RESULTS TO INDIVIDUALS: POINTS-TO-CONSIDER

Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity Mapping

Genetic and Physiological Data Implicating the New Human Gene G72 and the Gene for D-Amino Acid Oxidase in Schizophrenia

GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

Large-scale candidate gene study to identify genetic risk factors predictive of paliperidone treatment response in patients with schizophrenia

A survey of information literacy credit courses in US academic libraries: Prevalence and characteristics

SULT4A1 haplotype: conflicting results on its role as a biomarker of antipsychotic response

Polymorphisms in the multiple drug resistance protein 1 and in P-glycoprotein 1 are associated with time to event outcomes in patients with advanced multiple myeloma treated with bortezomib and pegylated liposomal doxorubicin

A survey of information literacy credit courses in US academic libraries

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness

Predisposing Gene for Early-Onset Prostate Cancer, Localized on Chromosome 1q42.2-43

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3 , encoding P-cadherin

Effect of the Cytochrome P450 2C19 Inhibitor Omeprazole on the Pharmacokinetics and Safety Profile of Bortezomib in Patients with Advanced Solid Tumours, Non-Hodgkin’s Lymphoma or Multiple Myeloma

PhRMA White Paper on ADME Pharmacogenomics

Bilateral Dacryoadenitis: Don’t Forget Tuberculosis

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter

Urgent care centers and virtual visits help avoid unnecessary trips to the ER

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