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Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studies
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title
Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studies
(English)
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author
Gianluca Severi
object named as
Gianluca Severi
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4
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Lesley McGuffog
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6
object named as
Lesley McGuffog
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Graham Giles
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22
object named as
Graham G. Giles
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John Hopper
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21
object named as
John L. Hopper
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Douglas F. Easton
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23
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Douglas F. Easton
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Melissa C. Southey
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Melissa C. Southey
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Dallas R. English
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20
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Dallas R. English
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Antonis C Antoniou
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2
object named as
Antonis C. Antoniou
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Rosalind Eeles
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3
object named as
Rosalind A. Eeles
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Margaret R E McCredie
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16
object named as
Margaret R. McCredie
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David P Dearnaley
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10
object named as
David P. Dearnaley
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Robert J MacInnis
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1
object named as
Robert J. MacInnis
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Michelle Guy
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5
object named as
Michelle Guy
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Audrey T. Ardern-Jones
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11
object named as
Audrey T. Ardern-Jones
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Lynne T O'Brien
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8
object named as
Lynne T. O'Brien
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Alan Horwich
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12
object named as
Alan Horwich
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Robert Huddart
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15
object named as
Robert A. Huddart
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Vincent Khoo
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13
object named as
Vincent S. Khoo
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author name string
Amanda L. Hall
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7
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Rosemary A. Wilkinson
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9
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Christopher C. Parker
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14
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Charmaine Smith
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17
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Margaret P. Staples
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19
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language of work or name
English
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publication date
2009
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published in
Genetic Epidemiology
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volume
34
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issue
1
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cites work
Asymptomatic incidence and duration of prostate cancer
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Rare germline mutations in the BRCA2 gene are associated with early-onset prostate cancer
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Mendelian inheritance of familial prostate cancer
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Oligogenic segregation analysis of hereditary prostate cancer pedigrees: evidence for multiple loci affecting age at onset
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Segregation analyses of 1,476 population-based Australian families affected by prostate cancer
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NBS1 is a prostate cancer susceptibility gene.
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A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer
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Multiple newly identified loci associated with prostate cancer susceptibility
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Admixture mapping identifies 8q24 as a prostate cancer risk locus in African-American men.
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Smoking and prostate cancer: Findings from an Australian case-control study
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Segregation analysis of prostate cancer in 1,719 white, African-American and Asian-American families in the United States and Canada
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Segregation analysis of prostate cancer in Sweden: support for dominant inheritance
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Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
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Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes
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Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
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Multiple regions within 8q24 independently affect risk for prostate cancer
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A mixed-model likelihood approximation on large pedigrees
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Prostate cancer screening, changing age-specific incidence trends and implications on familial risk
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A systematic review and meta-analysis of familial prostate cancer risk
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based on heuristic
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Probability calculations in pedigrees under complex modes of inheritance
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Programs for pedigree analysis: Mendel, Fisher, and dGene
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Evidence of an X-linked or recessive genetic component to prostate cancer risk
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The impact of family history on early detection of prostate cancer
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Genetics of prostate cancer: too many loci, too few genes
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Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance
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Longitudinal analysis of serial measurements of free and total PSA among men with and without prostatic cancer
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Evidence for autosomal dominant inheritance of prostate cancer
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7 January 2021
based on heuristic
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Pooled genome linkage scan of aggressive prostate cancer: results from the International Consortium for Prostate Cancer Genetics
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Cancer risks in BRCA2 mutation carriers
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https://api.crossref.org/works/10.1002%2FGEPI.20433
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Multiple loci identified in a genome-wide association study of prostate cancer
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Segregation Analysis of Prostate Cancer in France: Evidence for Autosomal Dominant Inheritance and Residual Brother-brother Dependence
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Autosomal dominant inheritance of prostate cancer: a confirmatory study
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stated in
Crossref
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https://api.crossref.org/works/10.1002%2FGEPI.20433
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple prostate cancer risk variants on 8q24
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGEPI.20433
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An investigation of the familial aspects of carcinoma of the prostate
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGEPI.20433
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGEPI.20433
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FGEPI.20433
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/GEPI.20433
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PubMed publication ID
19492347
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