(Q24615109)

Valgerdur Steinthorsdottir

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Patrick Sulem

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Solveig Gretarsdottir

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Gyda Bjornsdottir

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Andrea Maurichi

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Monica Rodolfo

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Yolanda Gilaberte

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Daníel F. Guðbjartsson

Daniel F Gudbjartsson

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Eduardo Nagore

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Esther de Vries

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Mario Santinami

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Heather H Nelson

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Rajiv Kumar

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Licia Rivoltini

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Lambertus A Kiemeney

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Kari Hemminki

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Annika Lindblom

Annika Lindblom

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Jeffrey Gulcher

Jeffrey R Gulcher

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Julius Gudmundsson

Kristrun R Benediktsdottir

Julius Gudmundsson

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Kristrun R Benediktsdottir

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Katja K H Aben

Katja K H Aben

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author name string

Simon N Stacey

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Gisli Masson

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Sigurjon A Gudjonsson

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Margret Jakobsdottir

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Asgeir Sigurdsson

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Bardur Sigurgeirsson

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Kristin Thorisdottir

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Rafn Ragnarsson

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Dominique Scherer

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Eugene Gurzau

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Rafael Botella-Estrada

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Virtudes Soriano

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Pablo Juberias

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Berta Saez

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Victoria Fuentelsaz

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Cristina Corredera

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Matilde Grasa

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Veronica Höiom

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Johannes J Bonenkamp

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Michelle M van Rossum

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Maria G Di Mauro

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Judith Wendt

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Pia Hochleitner

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Hubert Pehamberger

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Droplaug N Magnusdottir

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Hilma Holm

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Michael L Frigge

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Thorarinn Blondal

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Hjördis Bjarnason

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Kristleifur Kristjansson

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Ichiro Okamoto

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Johan Hansson

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José I Mayordomo

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Margaret R Karagas

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Jon H Olafsson

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

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language of work or name

English

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publication date

August 2009

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909-14

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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