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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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Association of Sly with sex-linked gene amplification during mouse evolution: a side effect of genomic conflict in spermatids?

Human molecular genetics, 2011-08, Vol.20 (15), p.3010-3021

2011

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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 ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence

Human molecular genetics, 2007-03, Vol.16 (6), p.600-608

2007

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Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements

Human molecular genetics, 2003-09, Vol.12 (17), p.2201-2208

2003

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African genetic diversity provides novel insights into evolutionary history and local adaptations

Human molecular genetics, 2018-08, Vol.27 (R2), p.R209-R218

2018

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Human BOULE gene rescues meiotic defects in infertile flies

Human molecular genetics, 2003-01, Vol.12 (2), p.169-175

2003

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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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Positive selection drives population differentiation in the skeletal genes in modern humans

Human molecular genetics, 2010-06, Vol.19 (12), p.2341-2346

2010

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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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Evolution of the sperm methylome of primates is associated with retrotransposon insertions and genome instability

Human molecular genetics, 2017-09, Vol.26 (18), p.3508-3519

2017

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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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Amino-acid changes acquired during evolution by olfactory receptor 912-93 modify the specificity of odorant recognition

Human molecular genetics, 2004-04, Vol.13 (7), p.771-780

2004

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Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity

Human molecular genetics, 2015-07, Vol.24 (13), p.3662-3678

2015

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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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A window into third-generation sequencing

Human molecular genetics, 2010-10, Vol.19 (R2), p.R227-R240

2010

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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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PAX6 in sensory development

Human molecular genetics, 2002-05, Vol.11 (10), p.1161-1167

2002

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Mitochondrial dynamics–fusion, fission, movement, and mitophagy–in neurodegenerative diseases

Human molecular genetics, 2009-10, Vol.18 (R2), p.R169-R176

2009

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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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Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary

Human molecular genetics, 2001-08, Vol.10 (17), p.1721-1728

2001

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

Association of Sly with sex-linked gene amplification during mouse evolution: a side effect of genomic conflict in spermatids?

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 ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence

Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements

African genetic diversity provides novel insights into evolutionary history and local adaptations

Human BOULE gene rescues meiotic defects in infertile flies

The genomic landscape of African populations in health and disease

Positive selection drives population differentiation in the skeletal genes in modern humans

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

Evolution of the sperm methylome of primates is associated with retrotransposon insertions and genome instability

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

Amino-acid changes acquired during evolution by olfactory receptor 912-93 modify the specificity of odorant recognition

Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity

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

A window into third-generation sequencing

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

PAX6 in sensory development

Mitochondrial dynamics–fusion, fission, movement, and mitophagy–in neurodegenerative diseases

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

Divergent evolution in M6P/IGF2R imprinting from the Jurassic to the Quaternary

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

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