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Efficient Conditional Mutation of the Vertebrate CENP-C Gene

Human molecular genetics, 1997-12, Vol.6 (13), p.2301-2308

1997

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Human mini-chromosomes with minimal centromeres

Human molecular genetics, 2000-07, Vol.9 (12), p.1891-1902

2000

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Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

Human molecular genetics, 1994-08, Vol.3 (8), p.1227-1237

1994

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The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes

Human molecular genetics, 1994-05, Vol.3 (5), p.771-778

1994

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Early and progressive circadian abnormalities in Huntington's disease sheep are unmasked by social environment

Human molecular genetics, 2014-07, Vol.23 (13), p.3375-3383

2014

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Structural Patching Fosters Divergence of Mitochondrial Ribosomes

Molecular biology and evolution, 2019-02, Vol.36 (2), p.207-219

2019

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Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Human molecular genetics, 2015-04, Vol.24 (8), p.2318-2329

2015

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Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Human molecular genetics, 2013-02, Vol.22 (4), p.832-841

2013

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Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Human molecular genetics, 2012-06, Vol.21 (12), p.2768-2778

2012

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Genetic landscape of auditory dysfunction

Human molecular genetics, 2018-08, Vol.27 (R2), p.R130-R135

2018

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Compensatory mutations restore fitness during the evolution of dihydrofolate reductase

Molecular biology and evolution, 2010-12, Vol.27 (12), p.2682-2690

2010

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Whole-Genome Resequencing of Experimental Populations Reveals Polygenic Basis of Egg-Size Variation in Drosophila melanogaster

Molecular biology and evolution, 2015-10, Vol.32 (10), p.2616-2632

2015

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The power to detect quantitative trait loci using resequenced, experimentally evolved populations of diploid, sexual organisms

Molecular biology and evolution, 2014-04, Vol.31 (4), p.1040-1055

2014

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The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Human molecular genetics, 2001-08, Vol.10 (17), p.1761-1766

2001

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A Conserved Ribosomal Protein Has Entirely Dissimilar Structures in Different Organisms

Molecular biology and evolution, 2024-01, Vol.41 (1)

2024

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Reduced striatal dopamine underlies the attention system dysfunction in neurofibromatosis-1 mutant mice

Human molecular genetics, 2010-11, Vol.19 (22), p.4515-4528

2010

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Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1

Human molecular genetics, 2013-10, Vol.22 (19), p.3947-3959

2013

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The carbohydrate-recognition domain of Dectin-2 is a C-type lectin with specificity for high mannose

Glycobiology (Oxford), 2006-05, Vol.16 (5), p.422-430

2006

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Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth

Human molecular genetics, 2015-09, Vol.24 (17), p.4775-4779

2015

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A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability

Human molecular genetics, 2017-10, Vol.26 (20), p.3869-3882

2017

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Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

Human molecular genetics, 2014-12, Vol.23 (23), p.6139-6146

2014

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Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study

Human molecular genetics, 2017-09, Vol.26 (17), p.3442-3450

2017

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Genetic control of the alternative pathway of complement in humans and age-related macular degeneration

Human molecular genetics, 2010-01, Vol.19 (1), p.209-215

2010

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Shared Genetic Signals of Hypoxia Adaptation in Drosophila and in High-Altitude Human Populations

Molecular biology and evolution, 2016-02, Vol.33 (2), p.501-517

2016

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Efficient Conditional Mutation of the Vertebrate CENP-C Gene

Human mini-chromosomes with minimal centromeres

Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes

Early and progressive circadian abnormalities in Huntington's disease sheep are unmasked by social environment

Structural Patching Fosters Divergence of Mitochondrial Ribosomes

Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Genetic landscape of auditory dysfunction

Compensatory mutations restore fitness during the evolution of dihydrofolate reductase

Whole-Genome Resequencing of Experimental Populations Reveals Polygenic Basis of Egg-Size Variation in Drosophila melanogaster

The power to detect quantitative trait loci using resequenced, experimentally evolved populations of diploid, sexual organisms

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

A Conserved Ribosomal Protein Has Entirely Dissimilar Structures in Different Organisms

Reduced striatal dopamine underlies the attention system dysfunction in neurofibromatosis-1 mutant mice

Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1

The carbohydrate-recognition domain of Dectin-2 is a C-type lectin with specificity for high mannose

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth

A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study

Genetic control of the alternative pathway of complement in humans and age-related macular degeneration

Shared Genetic Signals of Hypoxia Adaptation in Drosophila and in High-Altitude Human Populations

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