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An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome

Nature neuroscience, 2017-10, Vol.20 (10), p.1418

2017

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Parkinson's disease: genetics and pathogenesis

Annual review of pathology, 2011-01, Vol.6 (1), p.193-222

2011

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Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

Human molecular genetics, 2004-09, Vol.13 (17), p.1943-1949

2004

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Low testosterone is associated with disability in men with multiple sclerosis

Multiple sclerosis, 2014-10, Vol.20 (12), p.1584-1592

2014

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Value of coronary artery calcium score in reporting SPECT versus PET myocardial perfusion imaging

European heart journal cardiovascular imaging, 2021-07, Vol.22 (Supplement_3)

2021

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Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis

Nature genetics, 2018-08, Vol.50 (8), p.1081-1085

2018

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Genetic variation at CR1 increases risk of cerebral amyloid angiopathy

Neurology, 2012-01, Vol.78 (5), p.334

2012

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Entropy-based myocardial blood flow measurements using PET: a way to improve reproducibility

European heart journal cardiovascular imaging, 2021-07, Vol.22 (Supplement_3)

2021

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Preclinical characterisation of 111 In‐DTPA‐trastuzumab

British journal of pharmacology, 2009-02, Vol.143 (1), p.99-106

2009

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Neuropathologic intermediate phenotypes enhance association to Alzheimer susceptibility alleles

Neurology, 2009-04, Vol.72 (17), p.1495

2009

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Value of regional myocardial flow measurements using Rubidium-82 PET

European heart journal cardiovascular imaging, 2021-07, Vol.22 (Supplement_3)

2021

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Long-term prognosis of zero coronary artery calcium score in symptomatic low to intermediate risk patients

European heart journal cardiovascular imaging, 2021-07, Vol.22 (Supplement_3)

2021

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A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility

Nature genetics, 2005-10, Vol.37 (10), p.1113-1118

2005

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Admixture Mapping of an Allele Affecting Interleukin 6 Soluble Receptor and Interleukin 6 Levels

American journal of human genetics, 2007-04, Vol.80 (4), p.716-726

2007

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Radiolabeled Amino Acids: Basic Aspects and Clinical Applications in Oncology

The Journal of nuclear medicine (1978), 2001-03, Vol.42 (3), p.432-445

2001

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Apolipoprotein E and Change in Episodic Memory in Blacks and Whites

Neuroepidemiology, 2013-03, Vol.40 (3), p.211-219

2013

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An RNA profile identifies two subsets of multiple sclerosis patients differing in disease activity

Science translational medicine, 2012-09, Vol.4 (153), p.153ra131

2012

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Esophageal cancer: CT, endoscopic US, and FDG PET for assessment of response to neoadjuvant therapy--systematic review

Radiology, 2005-09, Vol.236 (3), p.841

2005

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Genome-wide association study of severity in multiple sclerosis: International Multiple Sclerosis Genetics Consortium

Genes and immunity, 2011-06, Vol.12 (8), p.615-625

De Jager, PL

2011

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[18F]FLT-PET in oncology: current status and opportunities

European journal of nuclear medicine and molecular imaging, 2004-12, Vol.31 (12), p.1659-1672

2004

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The value of FDG-PET in the detection, grading and response to therapy of soft tissue and bone sarcomas; a systematic review and meta-analysis

Cancer treatment reviews, 2004-02, Vol.30 (1), p.83-101

2004

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A High-Density Screen for Linkage in Multiple Sclerosis

American journal of human genetics, 2005-09, Vol.77 (3), p.454-467

2005

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Abstract P3-13-04: Radioactive seed localization in non-palpable breast cancer compared to wire-guided localization and radio-guided occult lesion localization: Results of a comparative study

Cancer research (Chicago, Ill.), 2016-02, Vol.76 (4_Supplement), p.P3-P3-13-04

2016

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Genetic Susceptibility for Ischemic Infarction and Arteriolosclerosis Based on Neuropathologic Evaluations

Cerebrovascular diseases (Basel, Switzerland), 2013-01, Vol.36 (3), p.181-188

2013

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An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome

Parkinson's disease: genetics and pathogenesis

Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping

Low testosterone is associated with disability in men with multiple sclerosis

Value of coronary artery calcium score in reporting SPECT versus PET myocardial perfusion imaging

Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis

Genetic variation at CR1 increases risk of cerebral amyloid angiopathy

Entropy-based myocardial blood flow measurements using PET: a way to improve reproducibility

Preclinical characterisation of 111 In‐DTPA‐trastuzumab

Neuropathologic intermediate phenotypes enhance association to Alzheimer susceptibility alleles

Value of regional myocardial flow measurements using Rubidium-82 PET

Long-term prognosis of zero coronary artery calcium score in symptomatic low to intermediate risk patients

A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility

Admixture Mapping of an Allele Affecting Interleukin 6 Soluble Receptor and Interleukin 6 Levels

Radiolabeled Amino Acids: Basic Aspects and Clinical Applications in Oncology

Apolipoprotein E and Change in Episodic Memory in Blacks and Whites

An RNA profile identifies two subsets of multiple sclerosis patients differing in disease activity

Esophageal cancer: CT, endoscopic US, and FDG PET for assessment of response to neoadjuvant therapy--systematic review

Genome-wide association study of severity in multiple sclerosis: International Multiple Sclerosis Genetics Consortium

[18F]FLT-PET in oncology: current status and opportunities

The value of FDG-PET in the detection, grading and response to therapy of soft tissue and bone sarcomas; a systematic review and meta-analysis

The expanding genetic overlap between multiple sclerosis and type I diabetes

A High-Density Screen for Linkage in Multiple Sclerosis

Abstract P3-13-04: Radioactive seed localization in non-palpable breast cancer compared to wire-guided localization and radio-guided occult lesion localization: Results of a comparative study

Genetic Susceptibility for Ischemic Infarction and Arteriolosclerosis Based on Neuropathologic Evaluations

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