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The anti-tubercular drug delamanid as a potential oral treatment for visceral leishmaniasis

eLife, 2016-05, Vol.5

2016

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DNA sequence-selective G-A cross-linking ADC payloads for use in solid tumour therapies

Communications biology, 2022-07, Vol.5 (1), p.741-741, Article 741

2022

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Novel pyridyl nitrofuranyl isoxazolines show antibacterial activity against multiple drug resistant Staphylococcus species

Bioorganic & medicinal chemistry, 2017-08, Vol.25 (15), p.3971-3979

2017

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Evaluating the level of nitroreductase activity in clinical Klebsiella pneumoniae isolates to support strategies for nitro drug and prodrug development

International journal of antimicrobial agents, 2019-11, Vol.54 (5), p.538-546

2019

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Abstract 1749: A new class of DNA sequence-selective G-A cross-linking antibody-drug conjugate (ADC) payloads

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.1749-1749

2022

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Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women

American journal of human genetics, 2012-09, Vol.91 (3), p.502-512

2012

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Rare coding variants pinpoint genes that control human hematological traits

PLoS genetics, 2017-08, Vol.13 (8), p.e1006925-e1006925

2017

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Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study

Epigenetics, 2022-12, Vol.17 (13), p.1976-1990

2022

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All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms

Genetics in medicine, 2017-05, Vol.19 (5), p.513-520

2017

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Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

American journal of human genetics, 2014-08, Vol.95 (2), p.183-193

2014

Volltextzugriff (PDF)

Collagen-Specific Molecular Magnetic Resonance Imaging of Prostate Cancer

International journal of molecular sciences, 2022-12, Vol.24 (1), p.711

2022

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Latent Class Models of Early-life Trauma and Incident Breast Cancer

Epidemiology (Cambridge, Mass.), 2022-09, Vol.33 (5), p.729

2022

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FAHN/SPG35: a narrow phenotypic spectrum across disease classifications

Brain (London, England : 1878), 2019-06, Vol.142 (6), p.1561-1572

2019

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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

PLoS genetics, 2019-12, Vol.15 (12), p.e1008500

2019

Volltextzugriff (PDF)

Early life trauma and adult leucocyte telomere length

Psychoneuroendocrinology, 2022-10, Vol.144, p.105876-105876, Article 105876

2022

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Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Human molecular genetics, 2014-04, Vol.23 (8), p.1957-1963

2014

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Communication and social interaction anxiety enhance interleukin-1 beta and cortisol reactivity during high-stakes public speaking

Psychoneuroendocrinology, 2018-08, Vol.94, p.83-90

2018

Volltextzugriff (PDF)

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature genetics, 2023-11, Vol.55 (11), p.1912-1919

2023

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Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease

The New England journal of medicine, 2014-07, Vol.371 (1), p.22-31

2014

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Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

Blood, 2013-07, Vol.122 (4), p.590-597

2013

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Mutations in SPTLC1 , encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

Nature genetics, 2001-03, Vol.27 (3), p.309-312

2001

Volltextzugriff (PDF)

Visual Functioning and Mortality of Age-Related Macular Degeneration Patients in a Colorado Cohort

Ophthalmology retina, 2023-11, Vol.7 (11), p.982-989

2023

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Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

Nature genetics, 2016-10, Vol.48 (10), p.1162-1170

2016

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The anti-tubercular drug delamanid as a potential oral treatment for visceral leishmaniasis

DNA sequence-selective G-A cross-linking ADC payloads for use in solid tumour therapies

Novel pyridyl nitrofuranyl isoxazolines show antibacterial activity against multiple drug resistant Staphylococcus species

Evaluating the level of nitroreductase activity in clinical Klebsiella pneumoniae isolates to support strategies for nitro drug and prodrug development

Abstract 1749: A new class of DNA sequence-selective G-A cross-linking antibody-drug conjugate (ADC) payloads

Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women

Rare coding variants pinpoint genes that control human hematological traits

Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study

All your data (effectively) belong to us: data practices among direct-to-consumer genetic testing firms

Pathogenic Variants for Mendelian and Complex Traits in Exomes of 6,517 European and African Americans: Implications for the Return of Incidental Results

Collagen-Specific Molecular Magnetic Resonance Imaging of Prostate Cancer

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Latent Class Models of Early-life Trauma and Incident Breast Cancer

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

Early life trauma and adult leucocyte telomere length

Quantifying rare, deleterious variation in 12 human cytochrome P450 drug-metabolism genes in a large-scale exome dataset

Communication and social interaction anxiety enhance interleukin-1 beta and cortisol reactivity during high-stakes public speaking

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease

Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

Mutations in SPTLC1 , encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I

Visual Functioning and Mortality of Age-Related Macular Degeneration Patients in a Colorado Cohort

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project

Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

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