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Comparative evaluation of a laboratory-developed real-time PCR assay and RealStar® Adenovirus PCR Kit for quantitative detection of human adenovirus

Virology journal, 2018-09, Vol.15 (1), p.149-149, Article 149

2018

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Lung cancer Intragenic ERBB2 kinase mutations in tumours

Nature, 2004-09, Vol.431 (7008), p.525-526

2004

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Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine

Nature medicine, 2023-10, Vol.29 (10), p.2438-2457

2023

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Global landscape of SARS-CoV-2 genomic surveillance and data sharing

Nature genetics, 2022-04, Vol.54 (4), p.499-507

2022

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Mutations of the BRAF gene in human cancer

Nature (London), 2002-06, Vol.417 (6892), p.949-954

2002

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Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Nature genetics, 2012-05, Vol.44 (5), p.491-501

2012

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Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles

Leukemia, 2011-10, Vol.25 (10), p.1555-1563

2011

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Neoadjuvant nivolumab or nivolumab plus ipilimumab in operable non-small cell lung cancer: the phase 2 randomized NEOSTAR trial

Nature medicine, 2021-03, Vol.27 (3), p.504-514

2021

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Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

Nature (London), 2009-10, Vol.461 (7265), p.809-813

2009

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Machine learning for diagnosis of myocardial infarction using cardiac troponin concentrations

Nature medicine, 2023-05, Vol.29 (5), p.1201-1210

2023

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β-Catenin activation synergizes with PTEN loss to cause bladder cancer formation

Oncogene, 2011-01, Vol.30 (2), p.178-189

2011

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Suppression subtractive hybridization and expression profiling identifies a unique set of genes overexpressed in non-small-cell lung cancer

Oncogene, 2004-10, Vol.23 (46), p.7734-7745

2004

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Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Nature genetics, 2013-02, Vol.45 (2), p.155-163

2013

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Acute Serotonin and Dopamine Depletion Improves Attentional Control: Findings from the Stroop Task

Neuropsychopharmacology (New York, N.Y.), 2007-07, Vol.32 (7), p.1600-1610

2007

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Epigenetic silencing of long non-coding RNA BM742401 in multiple myeloma: impact on prognosis and myeloma dissemination

Cancer cell international, 2020-08, Vol.20 (1), p.403-403, Article 403

2020

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Patient-reported outcome (PRO) results from the AGITG DOCTOR trial: a randomised phase 2 trial of tailored neoadjuvant therapy for resectable oesophageal adenocarcinoma

BMC cancer, 2022-03, Vol.22 (1), p.276-276, Article 276

2022

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Critical role for β7 integrins in formation of the gut-associated lymphoid tissue

Nature (London), 1996-07, Vol.382 (6589), p.366-370

1996

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CFH Variants Affect Structural and Functional Brain Changes and Genetic Risk of Alzheimer's Disease

Neuropsychopharmacology (New York, N.Y.), 2016-03, Vol.41 (4), p.1034-1045

2016

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Psoriasis

Nature reviews. Disease primers, 1997-08, Vol.350 (9074), p.349-353

Stern, Robert S

1997

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T cell homing to epithelial barriers in allergic disease

Nature medicine, 2012-05, Vol.18 (5), p.705-715

2012

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Autistic-like behavior, spontaneous seizures, and increased neuronal excitability in a Scn8a mouse model

Neuropsychopharmacology (New York, N.Y.), 2021-10, Vol.46 (11), p.2011-2020

2021

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Pathogen-Host Defense in the Evolution of Depression: Insights into Epidemiology, Genetics, Bioregional Differences and Female Preponderance

Neuropsychopharmacology (New York, N.Y.), 2017-01, Vol.42 (1), p.5-27

2017

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Comparative evaluation of a laboratory-developed real-time PCR assay and RealStar® Adenovirus PCR Kit for quantitative detection of human adenovirus

Lung cancer Intragenic ERBB2 kinase mutations in tumours

Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine

Global landscape of SARS-CoV-2 genomic surveillance and data sharing

Mutations of the BRAF gene in human cancer

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles

Neoadjuvant nivolumab or nivolumab plus ipilimumab in operable non-small cell lung cancer: the phase 2 randomized NEOSTAR trial

Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

Machine learning for diagnosis of myocardial infarction using cardiac troponin concentrations

β-Catenin activation synergizes with PTEN loss to cause bladder cancer formation

Maternal diabetes and risk of attention-deficit/hyperactivity disorder in offspring in a multinational cohort of 3.6 million mother-child pairs

Suppression subtractive hybridization and expression profiling identifies a unique set of genes overexpressed in non-small-cell lung cancer

Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus

Acute Serotonin and Dopamine Depletion Improves Attentional Control: Findings from the Stroop Task

Epigenetic silencing of long non-coding RNA BM742401 in multiple myeloma: impact on prognosis and myeloma dissemination

Patient-reported outcome (PRO) results from the AGITG DOCTOR trial: a randomised phase 2 trial of tailored neoadjuvant therapy for resectable oesophageal adenocarcinoma

Critical role for β7 integrins in formation of the gut-associated lymphoid tissue

CFH Variants Affect Structural and Functional Brain Changes and Genetic Risk of Alzheimer's Disease

Psoriasis

T cell homing to epithelial barriers in allergic disease

Autistic-like behavior, spontaneous seizures, and increased neuronal excitability in a Scn8a mouse model

Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance

Pathogen-Host Defense in the Evolution of Depression: Insights into Epidemiology, Genetics, Bioregional Differences and Female Preponderance

Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease

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