(Q57948414)

14

object named as

Jeffrey M Trent

0 references

author name string

Femke A de Snoo

1

0 references

Elizabeth M Gillanders

3

0 references

Loudewijk A Sandkuijl

4

0 references

Mary Pat Jones

5

0 references

Wilma Bergman

6

0 references

Clasine van der Drift

7

0 references

Inge van Leeuwen

8

0 references

Lenny van Mourik

9

0 references

Jeanet A C ter Huurne

10

0 references

Rune R Frants

11

0 references

Rein Willemze

12

0 references

Martijn H Breuning

13

0 references

Nelleke A Gruis

European Journal of Human Genetics

15

0 references

publication date

9 April 2008

0 references

published in

0 references

volume

16

0 references

page(s)

1135-1141

0 references

issue

9

0 references

exact match

https://scigraph.springernature.com/pub.10.1038/ejhg.2008.72

0 references

cites work

Geographical variation in the penetrance of CDKN2A mutations for melanoma

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

Genetic susceptibility to naevi – a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

Genetic predisposition to melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Familial atypical multiple mole-melanoma syndrome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

A cell cycle regulator potentially involved in genesis of many tumor types

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

The CDKN2A (p16) gene and human cancer.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Genetic testing for melanoma.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Germline p16 mutations in familial melanoma

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Genotype/phenotype and penetrance studies in melanoma families with germline CDKN2A mutations.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Excess cancer mortality in six Dutch pedigrees with the familial atypical multiple mole-melanoma syndrome from 1830 to 1994.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Inherited susceptibility to several cancers but absence of linkage between dysplastic nevus syndrome and CDKN2A in a melanoma family with a mutation in the CDKN2A ( P16INK4A ) gene

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

GRR: graphical representation of relationship errors

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

An Integrated Genetic Map for Linkage Analysis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

A combined linkage-physical map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Prospective risk of cancer in CDKN2A germline mutation carriers

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Atypical histologic features in melanocytic nevi

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Heritability and gene-environment interactions for melanocytic nevus density examined in a U.K. adolescent twin study.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021

A genome-wide scan for naevus count: linkage to CDKN2A and to other chromosome regions

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.72

7 January 2021