Lista de obras - Jeffrey M. Kidd - Dominio Público Uruguay

A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration

artículo científico publicado en 2011

A burst of segmental duplications in the genome of the African great ape ancestor

artículo científico publicado en 2009

A catalog of nonsynonymous polymorphism on mouse chromosome 16.

artículo científico publicado en 2005

A human genome structural variation sequencing resource reveals insights into mutational mechanisms

artículo científico publicado en 2010

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

artículo científico publicado en 2010

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

artículo científico publicado en 2010

A tale of two haplotypes: the EDA2R/AR Intergenic region is the most divergent genomic segment between Africans and East Asians in the human genome.

artículo científico publicado en 2012

An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome

scientific article published on 16 May 2019

Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs.

artículo científico publicado en 2018

Author Correction: Comparative and demographic analysis of orang-utan genomes

artículo científico publicado en 2022

Characterization of missing human genome sequences and copy-number polymorphic insertions

artículo científico publicado en 2010

Characterization of six human disease-associated inversion polymorphisms

artículo científico publicado en 2009

Comparative and demographic analysis of orang-utan genomes

artículo científico publicado en 2011

Comparison of village dog and wolf genomes highlights the role of the neural crest in dog domestication.

artículo científico publicado en 2018

Complete Khoisan and Bantu genomes from southern Africa

artículo científico publicado en 2010

Death and resurrection of the human IRGM gene

artículo científico publicado en 2009

Detecting and annotating genetic variations using the HugeSeq pipeline

artículo científico publicado en 2012

Detection and characterization of novel sequence insertions using paired-end next-generation sequencing

artículo científico publicado en 2010

Discovery and characterization of Alu repeat sequences via precise local read assembly

artículo científico publicado en 2015

Dog10K: the International Consortium of Canine Genome Sequencing

artículo científico publicado en 2019

Erratum: A burst of segmental duplications in the genome of the African great ape ancestor

artículo científico publicado en 2009

Evolutionary toggling of the MAPT 17q21.31 inversion region

artículo científico publicado en 2008

Extensive copy-number variation of the human olfactory receptor gene family

artículo científico publicado en 2008

Genetic recombination is targeted towards gene promoter regions in dogs.

artículo científico publicado en 2013

Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee

artículo científico publicado en 2011

Great ape genetic diversity and population history

artículo científico publicado en 2013

Haplotype sorting using human fosmid clone end-sequence pairs

artículo científico publicado en 2008

High-resolution human genome structure by single-molecule analysis

artículo científico publicado en 2010

Human copy number polymorphic genes

artículo científico publicado en 2008

Hunter-gatherer genomic diversity suggests a southern African origin for modern humans

artículo científico publicado en 2011

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

artículo científico publicado en 2020

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

artículo científico publicado en 2017

LINE-1 retrotransposition activity in human genomes

artículo científico publicado en 2010

Limited evidence for classic selective sweeps in African populations

artículo científico publicado en 2012

Mapping and sequencing of structural variation from eight human genomes

artículo científico publicado en 2008

Mapping copy number variation by population-scale genome sequencing

artículo científico publicado en 2011

Origin and recent expansion of an endogenous gammaretroviral lineage in domestic and wild canids

artículo científico publicado en 2019

Personalized copy number and segmental duplication maps using next-generation sequencing.

artículo científico publicado en 2009

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

artículo científico publicado en 2012

Population stratification of a common APOBEC gene deletion polymorphism

artículo científico publicado en 2007

Population-genetic properties of differentiated human copy-number polymorphisms

artículo científico publicado en 2011

Rapid, Paralog-Sensitive CNV Analysis of 2457 Human Genomes Using QuicK-mer2

scientific article published on 29 January 2020

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

artículo científico publicado en 2009

Sequencing Y chromosomes resolves discrepancy in time to common ancestor of males versus females

artículo científico publicado en 2013

Stable integrant-specific differences in bimodal HIV-1 expression patterns revealed by high-throughput analysis

artículo científico publicado en 2019

Structural diversity and African origin of the 17q21.31 inversion polymorphism

artículo científico publicado en 2012

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

artículo científico publicado en 2008

The genomic landscape of polymorphic human nuclear mitochondrial insertions

artículo científico publicado en 2014

Transcriptome sequencing from diverse human populations reveals differentiated regulatory architecture

artículo científico publicado en 2014

TypeTE: a tool to genotype mobile element insertions from whole genome resequencing data

artículo científico publicado en 2020

Variation of BMP3 contributes to dog breed skull diversity

artículo científico publicado en 2012

Lista de obras de Jeffrey M. Kidd

A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration

A burst of segmental duplications in the genome of the African great ape ancestor

A catalog of nonsynonymous polymorphism on mouse chromosome 16.

A human genome structural variation sequencing resource reveals insights into mutational mechanisms

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

A tale of two haplotypes: the EDA2R/AR Intergenic region is the most divergent genomic segment between Africans and East Asians in the human genome.

An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome

Analysis of the canid Y-chromosome phylogeny using short-read sequencing data reveals the presence of distinct haplogroups among Neolithic European dogs.

Author Correction: Comparative and demographic analysis of orang-utan genomes

Characterization of missing human genome sequences and copy-number polymorphic insertions

Characterization of six human disease-associated inversion polymorphisms

Comparative and demographic analysis of orang-utan genomes

Comparison of village dog and wolf genomes highlights the role of the neural crest in dog domestication.

Complete Khoisan and Bantu genomes from southern Africa

Death and resurrection of the human IRGM gene

Detecting and annotating genetic variations using the HugeSeq pipeline

Detection and characterization of novel sequence insertions using paired-end next-generation sequencing

Discovery and characterization of Alu repeat sequences via precise local read assembly

Dog10K: the International Consortium of Canine Genome Sequencing

Erratum: A burst of segmental duplications in the genome of the African great ape ancestor

Evolutionary toggling of the MAPT 17q21.31 inversion region

Extensive copy-number variation of the human olfactory receptor gene family

Genetic recombination is targeted towards gene promoter regions in dogs.

Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee

Great ape genetic diversity and population history

Haplotype sorting using human fosmid clone end-sequence pairs

High-resolution human genome structure by single-molecule analysis

Human copy number polymorphic genes

Hunter-gatherer genomic diversity suggests a southern African origin for modern humans

Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

Intersection of diverse neuronal genomes and neuropsychiatric disease: The Brain Somatic Mosaicism Network

LINE-1 retrotransposition activity in human genomes

Limited evidence for classic selective sweeps in African populations

Mapping and sequencing of structural variation from eight human genomes

Mapping copy number variation by population-scale genome sequencing

Origin and recent expansion of an endogenous gammaretroviral lineage in domestic and wild canids

Personalized copy number and segmental duplication maps using next-generation sequencing.

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation

Population stratification of a common APOBEC gene deletion polymorphism

Population-genetic properties of differentiated human copy-number polymorphisms

Rapid, Paralog-Sensitive CNV Analysis of 2457 Human Genomes Using QuicK-mer2

Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

Sequencing Y chromosomes resolves discrepancy in time to common ancestor of males versus females

Stable integrant-specific differences in bimodal HIV-1 expression patterns revealed by high-throughput analysis

Structural diversity and African origin of the 17q21.31 inversion polymorphism

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

The genomic landscape of polymorphic human nuclear mitochondrial insertions

Transcriptome sequencing from diverse human populations reveals differentiated regulatory architecture

TypeTE: a tool to genotype mobile element insertions from whole genome resequencing data

Variation of BMP3 contributes to dog breed skull diversity