The distribution and most recent common ancestor of the 17q21 inversion in humans (Q28748948)

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17 January 2020

title

The distribution and most recent common ancestor of the 17q21 inversion in humans (English)

1 reference

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17 January 2020

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17 January 2020

3

Elena Grigorenko

1 reference

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17 January 2020

17

Hui Li

1 reference

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23

Kenneth K Kidd

1 reference

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17 January 2020

4

David Gurwitz

1 reference

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17 January 2020

7

Csaba Barta

1 reference

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17 January 2020

author name string

Michael P Donnelly

1

1 reference

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17 January 2020

Syed Qasim Mehdi

5

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17 January 2020

Sylvester L B Kajuna

6

1 reference

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17 January 2020

Selemani Kungulilo

8

1 reference

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17 January 2020

N J Karoma

9

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17 January 2020

Ru-Band Lu

10

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17 January 2020

Olga V Zhukova

11

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17 January 2020

Jong-Jin Kim

12

1 reference

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17 January 2020

David Comas

13

1 reference

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17 January 2020

Marcello Siniscalco

14

1 reference

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17 January 2020

Maria New

15

1 reference

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17 January 2020

Peining Li

16

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17 January 2020

Vangelis G Manolopoulos

18

1 reference

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17 January 2020

William C Speed

19

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17 January 2020

Haseena Rajeevan

20

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17 January 2020

Andrew J Pakstis

21

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17 January 2020

Judith R Kidd

22

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17 January 2020

language of work or name

English

0 references

publication date

28 January 2010

1 reference

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American Journal of Human Genetics

17 January 2020

published in

1 reference

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17 January 2020

volume

86

1 reference

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17 January 2020

issue

2

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17 January 2020

page(s)

161-171

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Evolutionary toggling of the MAPT 17q21.31 inversion region

17 January 2020

cites work

1 reference

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

16 March 2017

1 reference

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A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

16 March 2017

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A New Statistical Method for Haplotype Reconstruction from Population Data

16 March 2017

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Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes

16 March 2017

1 reference

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Worldwide human relationships inferred from genome-wide patterns of variation

16 March 2017

1 reference

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A comparison of bayesian methods for haplotype reconstruction from population genotype data

7 April 2017

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

7 April 2017

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A common inversion under selection in Europeans

7 April 2017

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Tau-mediated neurodegeneration in Alzheimer's disease and related disorders

7 April 2017

1 reference

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The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

7 April 2017

1 reference

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Standardized subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, accounting for atypical and duplicated samples and pairs of close relatives.

3 June 2018

1 reference

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

3 June 2018

1 reference

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

3 June 2018

1 reference

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The H2 MAPT haplotype is associated with familial frontotemporal dementia.

3 June 2018

1 reference

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

3 June 2018

1 reference

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Tau gene (MAPT) sequence variation among primates

3 June 2018

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Linkage disequilibrium and association of MAPT H1 in Parkinson disease

3 June 2018

1 reference

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Tau haplotypes regulate transcription and are associated with Parkinson's disease.

3 June 2018

1 reference

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Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.

3 June 2018

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Role of ethnicity on the association of MAPT H1 haplotypes and subhaplotypes in Parkinson's disease

3 June 2018

1 reference

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The architecture of the tau haplotype block in different ethnicities

27 November 2018

1 reference

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

27 November 2018

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Further extension of the H1 haplotype associated with progressive supranuclear palsy

27 November 2018

1 reference

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

27 November 2018

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Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

27 November 2018

1 reference

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The tau H2 haplotype is almost exclusively Caucasian in origin

27 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20116045

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20116045

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20116045

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2010.01.007

2 references

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17 January 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20116045%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

2 references