(Q34695793)

4 August 2017

title

Efficient mapping of mendelian traits in dogs through genome-wide association (English)

1 reference

genome-wide association study

4 August 2017

main subject

0 references

author

Elinor K. Karlsson

1

1 reference

4 August 2017

20

Kerstin Lindblad-Toh

0 references

Gerli Rosengren Pielberg

9

Gerli Rosengren Pielberg

0 references

Åke Hedhammar

16

Ake Hedhammar

0 references

Eric Lander

17

Eric S Lander

1 reference

4 August 2017

13

Jill P Mesirov

1 reference

4 August 2017

Claire M Wade

3

0 references

Olle Kämpe

Olle Kämpe

15

0 references

Göran Andersson

18

Göran Andersson

1 reference

4 August 2017

19

Leif Andersson

1 reference

4 August 2017

8

Nick Patterson

1 reference

4 August 2017

5

Michael C Zody

1 reference

Nicolette H C Salmon Hillbertz

4 August 2017

4

Nicolette H C Salmon Hillbertz

1 reference

4 August 2017

14

Henrik von Euler

1 reference

4 August 2017

7

Tara M Biagi

1 reference

4 August 2017

10

Edward J Kulbokas

1 reference

4 August 2017

11

Kenine E Comstock

1 reference

4 August 2017

Izabella Baranowska

2

1 reference

4 August 2017

Nathan Anderson

6

1 reference

4 August 2017

Evan T Keller

12

1 reference

4 August 2017

language of work or name

English

0 references

publication date

30 September 2007

1 reference

4 August 2017

1 reference

4 August 2017

volume

39

1 reference

4 August 2017

issue

11

1 reference

4 August 2017

page(s)

1321-1328

1 reference

Structural organization of the human microphthalmia-associated transcription factor gene containing four alternative promoters.

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

Genome sequence, comparative analysis and haplotype structure of the domestic dog

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Extensive and breed-specific linkage disequilibrium in Canis familiaris

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Genetic structure of the purebred domestic dog

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Population structure and eigenanalysis

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Autosomal dominant mutation causing the dorsal ridge predisposes for dermoid sinus in Rhodesian ridgeback dogs

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

The genetic basis of mammalian neurulation.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Comparison of the expression patterns of several fibroblast growth factors during chick gastrulation and neurulation.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

FGF8 initiates inner ear induction in chick and mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

https://api.crossref.org/works/10.1038%2FNG.2007.10

1 reference

7 January 2021

Exclusion of EDNRB and KIT as the basis for white spotting in Border Collies

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Analysis of the inheritance of white spotting and the evaluation of KIT and EDNRB as spotting loci in Dutch boxer dogs

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Tietz syndrome (hypopigmentation/deafness) caused by mutation of MITF

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Melanocytes and the microphthalmia transcription factor network

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Microphthalamia-associated transcription factor: a critical regulator of pigment cell development and survival.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

MITF: master regulator of melanocyte development and melanoma oncogene

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Melanocyte-specific microphthalmia-associated transcription factor isoform activates its own gene promoter through physical interaction with lymphoid-enhancing factor 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

The transcription factor onecut-2 controls the microphthalmia-associated transcription factor gene

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Dysgenesis of melanocytes and cochlear dysfunction in mutant microphthalmia (mi) mice

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Deafness prevalence and pigmentation and gender associations in dog breeds at risk

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

A late wave of melanoblast differentiation and rostrocaudal migration revealed in patch and rump-white embryos

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

The UCSC Genome Browser Database

1 reference

https://api.crossref.org/works/10.1038%2FNG.2007.10

7 January 2021

Identifiers

DOI

10.1038/NG.2007.10

1 reference

4 August 2017

1 reference