New common variants affecting susceptibility to basal cell carcinoma (Q24615109)

64

0 references

Augustine Kong

63

0 references

Gudmar Thorleifsson

5

0 references

Unnur Þorsteinsdóttir

Valgerdur Steinthorsdottir

61

0 references

42

0 references

Patrick Sulem

2

0 references

Solveig Gretarsdottir

40

0 references

Thorunn Rafnar

60

0 references

Jona Saemundsdottir

45

0 references

Peter Rudnai

15

0 references

Kvetoslava Koppová

17

0 references

Gyda Bjornsdottir

Gyda Bjornsdottir

48

0 references

Andrea Maurichi

Andrea Maurichi

34

0 references

Monica Rodolfo

Monica Rodolfo

51

0 references

Yolanda Gilaberte

Yolanda Gilaberte

22

0 references

Daníel F. Guðbjartsson

Daniel F Gudbjartsson

8

0 references

Eduardo Nagore

Eduardo Nagore

54

0 references

Esther de Vries

Esther de Vries

31

0 references

Mario Santinami

Mario Santinami

32

0 references

Heather H. Nelson

Heather H Nelson

58

0 references

Rajiv Kumar

Rajiv Kumar

56

0 references

Licia Rivoltini

Licia Rivoltini

50

0 references

Lambertus Kiemeney

Lambertus A Kiemeney

52

0 references

Kari Hemminki

14

Kari Hemminki

0 references

Annika Lindblom

27

Annika Lindblom

0 references

Jeffrey Gulcher

59

Jeffrey R Gulcher

0 references

Julius Gudmundsson

38

Kristrun R Benediktsdottir

Julius Gudmundsson

0 references

10

Kristrun R Benediktsdottir

0 references

Katja K H Aben

30

Katja K H Aben

0 references

author name string

Simon N Stacey

1

0 references

Gisli Masson

3

0 references

Sigurjon A Gudjonsson

4

0 references

Margret Jakobsdottir

6

0 references

Asgeir Sigurdsson

7

0 references

Bardur Sigurgeirsson

9

0 references

Kristin Thorisdottir

11

0 references

Rafn Ragnarsson

12

0 references

Dominique Scherer

13

0 references

Eugene Gurzau

16

0 references

Rafael Botella-Estrada

18

0 references

Virtudes Soriano

19

0 references

Pablo Juberias

20

0 references

Berta Saez

21

0 references

Victoria Fuentelsaz

23

0 references

Cristina Corredera

24

0 references

Matilde Grasa

25

0 references

Veronica Höiom

26

0 references

Johannes J Bonenkamp

28

0 references

Michelle M van Rossum

29

0 references

Maria G Di Mauro

33

0 references

Judith Wendt

35

0 references

Pia Hochleitner

36

0 references

Hubert Pehamberger

37

0 references

Droplaug N Magnusdottir

39

0 references

Hilma Holm

41

0 references

Michael L Frigge

43

0 references

Thorarinn Blondal

44

0 references

Hjördis Bjarnason

46

0 references

Kristleifur Kristjansson

47

0 references

Ichiro Okamoto

49

0 references

Johan Hansson

53

0 references

José I Mayordomo

55

0 references

Margaret R Karagas

57

0 references

Jon H Olafsson

MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B

62

0 references

language of work or name

English

0 references

publication date

August 2009

0 references

published in

Nature Genetics

0 references

volume

41

0 references

issue

8

0 references

page(s)

909-14

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=2973331

Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

The genetic basis of Weber-Cockayne epidermolysis bullosa simplex

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Genetic determinants of hair, eye and skin pigmentation 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=2973331

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Many sequence variants affecting diversity of adult human height

7 April 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038/NG.412

Quantifying heterogeneity in a meta-analysis

22 April 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038/NG.412

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

A common variant on chromosome 9p21 affects the risk of myocardial infarction

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Detection of sharing by descent, long-range phasing and haplotype imputation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Basal cell carcinomas: attack of the hedgehog

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Variants of the MATP/SLC45A2 gene are protective for melanoma in the French population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

A prospective study of telomere length and the risk of skin cancer

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Two newly identified genetic determinants of pigmentation in Europeans

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

The human keratins: biology and pathology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Nevus size and number are associated with telomere length and represent potential markers of a decreased senescence in vivo.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Diseases of epidermal keratins and their linker proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

The regulation of INK4/ARF in cancer and aging

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

SLC45A2: a novel malignant melanoma-associated gene

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2973331

Epidermolysis Bullosa Simplex with mottled pigmentation: mutation analysis in the first reported Hispanic pedigree with the largest single generation of affected individuals to date

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19578363

12 December 2020

inferred from PubMed ID database lookup

A novel autosomal partially dominant mutation designated G476D in the keratin 5 gene causing epidermolysis bullosa simplex Weber-Cockayne type: a family study with a genetic twist

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19578363

12 December 2020

inferred from PubMed ID database lookup

Genetics of melanoma predisposition

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19578363

12 December 2020

inferred from PubMed ID database lookup

The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases.

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.412

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NG.412

1 reference

Dimensions Publication ID

1033015538

0 references

1 reference

1 reference

PubMed publication ID

19578363

1 reference