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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

Human molecular genetics, 2004-04, Vol.13 (suppl-1), p.R57-R64

2004

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Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

Human molecular genetics, 2008-04, Vol.17 (8), p.1127-1136

2008

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Challenges in human genetic diversity: demographic history and adaptation

Human molecular genetics, 2007-10, Vol.16 (R2), p.R134-R139

2007

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The genomic landscape of African populations in health and disease

Human molecular genetics, 2017-10, Vol.26 (R2), p.R225-R236

2017

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Extensive contribution of embryonic stem cells to the development of an evolutionarily divergent host

Human molecular genetics, 2008-01, Vol.17 (1), p.27-37

2008

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Exosomes and microvesicles: extracellular vesicles for genetic information transfer and gene therapy

Human molecular genetics, 2012-10, Vol.21 (1), p.R125-R134

2012

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LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice

Human molecular genetics, 2011-11, Vol.20 (21), p.4209-4223

2011

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TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1

Human molecular genetics, 2011-04, Vol.20 (7), p.1400-1410

2011

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ROS-dependent regulation of Parkin and DJ-1 localization during oxidative stress in neurons

Human molecular genetics, 2012-11, Vol.21 (22), p.4888-4903

2012

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Evidence for an oligogenic basis of amyotrophic lateral sclerosis

Human molecular genetics, 2012-09, Vol.21 (17), p.3776-3784

2012

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Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

Human molecular genetics, 2012-01, Vol.21 (2), p.371-383

2012

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Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways

Human molecular genetics, 2011-10, Vol.20 (19), p.3852-3866

2011

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Exome sequencing and complex disease: practical aspects of rare variant association studies

Human molecular genetics, 2012-10, Vol.21 (1), p.R1-R9

2012

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KASH protein Syne-2/Nesprin-2 and SUN proteins SUN1/2 mediate nuclear migration during mammalian retinal development

Human molecular genetics, 2011-03, Vol.20 (6), p.1061-1073

2011

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Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy

Human molecular genetics, 2010-12, Vol.19 (24), p.4861-4870

2010

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Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Human molecular genetics, 2012-10, Vol.21 (20), p.4419-4430

2012

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Genome-wide association study of circulating vitamin D levels

Human molecular genetics, 2010-07, Vol.19 (13), p.2739-2745

2010

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Broad activation of the ubiquitin―proteasome system by Parkin is critical for mitophagy

Human molecular genetics, 2011-05, Vol.20 (9), p.1726-1737

2011

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DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific

Human molecular genetics, 2009-11, Vol.18 (21), p.4046-4053

2009

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The Mouse Mid1 Gene: Implications for the Pathogenesis of Opitz Syndrome and the Evolution of the Mammalian Pseudoautosomal Region

Human molecular genetics, 1998-03, Vol.7 (3), p.489-499

1998

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DNA methylation and gene expression differences in children conceived in vitro or in vivo

Human molecular genetics, 2009-10, Vol.18 (20), p.3769-3778

2009

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Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease

Human molecular genetics, 2011-12, Vol.20 (23), p.4515-4529

2011

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MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function

Human molecular genetics, 2011-08, Vol.20 (15), p.3067-3078

2011

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Early heart failure in the SMNΔ7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery

Human molecular genetics, 2010-07, Vol.19 (20), p.3895-3905

2010

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Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies

Challenges in human genetic diversity: demographic history and adaptation

The genomic landscape of African populations in health and disease

Extensive contribution of embryonic stem cells to the development of an evolutionarily divergent host

Exosomes and microvesicles: extracellular vesicles for genetic information transfer and gene therapy

LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice

TAR DNA-binding protein 43 (TDP-43) regulates stress granule dynamics via differential regulation of G3BP and TIA-1

ROS-dependent regulation of Parkin and DJ-1 localization during oxidative stress in neurons

Evidence for an oligogenic basis of amyotrophic lateral sclerosis

Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

Characterization of the CLEAR network reveals an integrated control of cellular clearance pathways

Exome sequencing and complex disease: practical aspects of rare variant association studies

KASH protein Syne-2/Nesprin-2 and SUN proteins SUN1/2 mediate nuclear migration during mammalian retinal development

Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy

Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis

Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans

Genome-wide association study of circulating vitamin D levels

Broad activation of the ubiquitin―proteasome system by Parkin is critical for mitophagy

DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific

The Mouse Mid1 Gene: Implications for the Pathogenesis of Opitz Syndrome and the Evolution of the Mammalian Pseudoautosomal Region

DNA methylation and gene expression differences in children conceived in vitro or in vivo

Impaired mitochondrial biogenesis, defective axonal transport of mitochondria, abnormal mitochondrial dynamics and synaptic degeneration in a mouse model of Alzheimer's disease

MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function

Early heart failure in the SMNΔ7 model of spinal muscular atrophy and correction by postnatal scAAV9-SMN delivery

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