(Q24658093)

6

0 references

Evan E. Eichler

20

0 references

Francesca Antonacci

Francesca Antonacci

4

0 references

Jeffrey M. Kidd

Jeffrey M Kidd

8

0 references

Mario Ventura

Mario Ventura

17

0 references

John Anthony Hardy

18

John Hardy

0 references

Michael C. Zody

1

Michael C Zody

0 references

Wesley C Warren

19

Wesley C Warren

0 references

Ladeana Hillier

5

LaDeana W Hillier

0 references

Richard K. Wilson

14

Richard K Wilson

0 references

Jarret Glasscock

13

Jarret Glasscock

0 references

Amr Abouelleil

10

Amr Abouelleil

0 references

Zhaoshi Jiang

2

Zhaoshi Jiang

0 references

Amy Denise Reily

15

Amy Denise Reily

0 references

author name string

Hon-Chung Fung

3

0 references

Tina A Graves

7

0 references

Ze Cheng

9

0 references

Lin Chen

11

0 references

John Wallis

12

0 references

Jaime Duckworth

A second generation human haplotype map of over 3.1 million SNPs

16

0 references

language of work or name

English

0 references

publication date

September 2008

0 references

published in

Nature Genetics

0 references

volume

40

0 references

page(s)

1076-83

0 references

issue

9

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Global variation in copy number in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Low nucleotide diversity in chimpanzees and bonobos

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

The neighbor-joining method: a new method for reconstructing phylogenetic trees

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Mapping Human Genetic Ancestry

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Initial sequence of the chimpanzee genome and comparison with the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Detection of large-scale variation in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Analysis of the DNA sequence and duplication history of human chromosome 15

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A genome-wide comparison of recent chimpanzee and human segmental duplications

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Large-scale copy number polymorphism in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Genetic structure of human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A recurrent inversion on the eutherian X chromosome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

The genomic record of Humankind's evolutionary roots

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Genotype, haplotype and copy-number variation in worldwide human populations

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A common inversion under selection in Europeans

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Recent segmental duplications in the human genome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Hominoid chromosomal rearrangements on 17q map to complex regions of segmental duplication.

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Recurrent duplication-driven transposition of DNA during hominoid evolution

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Evidence suggesting that Homo neanderthalensis contributed the H2 MAPT haplotype to Homo sapiens

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Recent segmental duplications in the working draft assembly of the brown Norway rat.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Segmental duplications: organization and impact within the current human genome project assembly

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Miropeats: graphical DNA sequence comparisons.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

30 May 2018

1 reference

The structure of the tau haplotype in controls and in progressive supranuclear palsy.

21 January 2018

1 reference

A survey of genetic human cortical gene expression

21 January 2018

1 reference

Genetic evidence for the involvement of tau in progressive supranuclear palsy

21 January 2018

1 reference

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

21 January 2018

1 reference

Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.

21 January 2018

1 reference

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.

21 January 2018

1 reference

The genus Pan: population genetics of an endangered outgroup.

21 January 2018

1 reference

Ancestral reconstruction of segmental duplications reveals punctuated cores of human genome evolution.

21 January 2018

1 reference

Chromosomal evolution: inversions: the chicken or the egg?

21 January 2018

1 reference

Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions

21 January 2018

1 reference

CLUSTAL V: multiple alignment of DNA and protein sequences.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2684794

The tau H2 haplotype is almost exclusively Caucasian in origin

28 November 2018

1 reference

12 December 2020

Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits

1 reference

12 December 2020

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

1 reference

12 December 2020

Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients

1 reference

12 December 2020