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Evolutionary evidence of the effect of rare variants on disease etiology

Clinical genetics, 2011-03, Vol.79 (3), p.199-206

2011

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Mutations of the GREAT gene cause cryptorchidism

Human molecular genetics, 2002-09, Vol.11 (19), p.2309-2318

2002

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A transgenic insertion causing cryptorchidism in mice

Genesis (New York, N.Y. : 2000), 2001-05, Vol.30 (1), p.26-35

2001

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Analysis of the phenotypic effects of B chromosomes in a natural population of Metagagrella tenuipes (Arachnida: Opiliones)

Heredity, 2000-02, Vol.84 (2), p.209-217

2000

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Shifting Paradigm of Association Studies: Value of Rare Single-Nucleotide Polymorphisms

American journal of human genetics, 2008-01, Vol.82 (1), p.100-112

2008

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Missense mutations in cancer suppressor gene TP53 are colocalized with exonic splicing enhancers (ESEs)

Mutation research, 2004-10, Vol.554 (1), p.175-183

2004

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Double Insertion of Homogeneously Staining Regions in Chromosome 1 of Wild Mus musculus musculus: Effects on Chromosome Pairing and Recombination

The Journal of heredity, 1990-03, Vol.81 (2), p.91-95

1990

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Cytogenetic Studies on Siberian Spiders

Hereditas, 1995-10, Vol.122 (3), p.211-220

1995

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The origin of a double insertion of homogeneously staining regions in the house mouse ( )

Heredity, 1990-10, Vol.65 (2), p.265-267

1990

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Unusual heteromorphic bivalents in the common vole (Microtus arvalis) from Belorussia

Cytogenetic and genome research, 1992-01, Vol.60 (2), p.123-127

1992

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Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse

Chromosoma, 1990-09, Vol.99 (5), p.365-370

1990

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Synaptic interrelationships between the segments of the heteromorphic bivalent in double heterozygotes for paracentric inversions in chromosome 1 of the house mouse

Chromosoma, 1992-03, Vol.101 (5-6), p.374-379

1992

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Positional control of chiasma distribution in the house mouse. Chiasma distribution in mice homozygous and heterozygous for an inversion in chromosome 1

Heredity, 1991-06, Vol.66 (3), p.453-458

1991

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In silico functional profiling of individual prostate cancer tumors: many genes, few functions

Cancer genomics & proteomics, 2012-05, Vol.9 (3), p.109-114

2012

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Effect of double insertion of homogeneously stained regions in chromosome 1 of the house mouse on recombination frequency

Genetika, 1989-02, Vol.25 (2), p.220

1989

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Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome

Human molecular genetics, 2006-04, Vol.15 (7), p.1143-1150

2006

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Missense Mutations in hMLH1 and hMSH2 Are Associated with Exonic Splicing Enhancers

American journal of human genetics, 2003-11, Vol.73 (5), p.1157-1161

2003

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Predicting the oncogenicity of missense mutations reported in the International Agency for Cancer Research (IARC) mutation database on p53

Human mutation, 2005-11, Vol.26 (5), p.446-454

2005

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Chiasmata distribution in the normal karyotype of mice

Genetika, 1991-02, Vol.27 (2), p.247

1991

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STAGGERED CLINES IN A HYBRID ZONE BETWEEN TWO CHROMOSOME RACES OF THE HARVESTMAN GAGRELLOPSIS NODULIFERA (ARACHNIDA: OPILIONES)

Evolution, 2000-02, Vol.54 (1), p.176-190

2000

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Cytogenetic consequences of hybridization between wild and laboratory mice

Genetika, 1986-05, Vol.22 (5), p.855

1986

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Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse

Genetika, 1990-07, Vol.26 (7), p.1279

1990

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Why does the X chromosome lag behind autosomes in GWAS findings?

PLoS genetics, 2023-02, Vol.19 (2), p.e1010472-e1010472

2023

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Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

Nature genetics, 2008-05, Vol.40 (5), p.616-622

2008

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Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases

PLoS genetics, 2015-07, Vol.11 (7), p.e1005371

2015

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Evolutionary evidence of the effect of rare variants on disease etiology

Mutations of the GREAT gene cause cryptorchidism

A transgenic insertion causing cryptorchidism in mice

Analysis of the phenotypic effects of B chromosomes in a natural population of Metagagrella tenuipes (Arachnida: Opiliones)

Shifting Paradigm of Association Studies: Value of Rare Single-Nucleotide Polymorphisms

Missense mutations in cancer suppressor gene TP53 are colocalized with exonic splicing enhancers (ESEs)

Double Insertion of Homogeneously Staining Regions in Chromosome 1 of Wild Mus musculus musculus: Effects on Chromosome Pairing and Recombination

Cytogenetic Studies on Siberian Spiders

The origin of a double insertion of homogeneously staining regions in the house mouse ( )

Unusual heteromorphic bivalents in the common vole (Microtus arvalis) from Belorussia

Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse

Synaptic interrelationships between the segments of the heteromorphic bivalent in double heterozygotes for paracentric inversions in chromosome 1 of the house mouse

Positional control of chiasma distribution in the house mouse. Chiasma distribution in mice homozygous and heterozygous for an inversion in chromosome 1

In silico functional profiling of individual prostate cancer tumors: many genes, few functions

Effect of double insertion of homogeneously stained regions in chromosome 1 of the house mouse on recombination frequency

Strength of the purifying selection against different categories of the point mutations in the coding regions of the human genome

Missense Mutations in hMLH1 and hMSH2 Are Associated with Exonic Splicing Enhancers

Predicting the oncogenicity of missense mutations reported in the International Agency for Cancer Research (IARC) mutation database on p53

Chiasmata distribution in the normal karyotype of mice

STAGGERED CLINES IN A HYBRID ZONE BETWEEN TWO CHROMOSOME RACES OF THE HARVESTMAN GAGRELLOPSIS NODULIFERA (ARACHNIDA: OPILIONES)

Cytogenetic consequences of hybridization between wild and laboratory mice

Synapsis in single and double heterozygotes for partially overlapping inversions in chromosome 1 of the house mouse

Why does the X chromosome lag behind autosomes in GWAS findings?

Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1

Allelic Spectra of Risk SNPs Are Different for Environment/Lifestyle Dependent versus Independent Diseases

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