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Nazneen Rahman

Veröffentlichungen von Nazneen Rahman zu Rahman, Nazneen ->
weitere Veröffentlichungen von Nazneen Rahman:
Instant notes in genetics: P. C. Winter, G. I. Hickey and H. L. Fletcher (1999)
A new gene on the X involved in Fanconi anemia (2004)
THE GENETICS OF BREAST CANCER SUSCEPTIBILITY (1998)
Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21 (1996)
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B (2004)
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles (2006)
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles (2006)
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth (2007)
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene (2007)
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer (2007)
Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations (2002)
Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk (2007)
A common coding variant in CASP8 is associated with breast cancer risk (2007)
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (2007)
Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A (2007)
Veröffentlichungen zu Rahman, Nazneen
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1
Rahman, Nazneen Instant notes in genetics: P. C. Winter, G. I. Hickey and H. L. Fletcher
in: Human genetics , ISSN 1432-1203, Vol. 104 (4. 1999), p. 358-358
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1999
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2
Rahman, Nazneen, Ashworth, Alan A new gene on the X involved in Fanconi anemia
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 36, No. 11 (2004), p. 1142-1143
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2004
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3
Rahman, Nazneen., Stratton, Michael R.. THE GENETICS OF BREAST CANCER SUSCEPTIBILITY
in: Annual Review of Genetics, in: Annual Review of Genetics. - Palo Alto, Calif., ISSN 0066-4197 Vol. 32 (1998), p. 95-121
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1998
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4
Rahman, Nazneen, Arbour, Laura, ... Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 13, No. 4 (1996), p. 461-463
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1996
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5
Hanks, Sandra, Coleman, Kim, ... Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 36, No. 11 (2004), p. 1159-1161
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2004
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6
Renwick, Anthony, Thompson, Deborah, ... ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 38, No. 8 (2006), p. 873-875
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2006
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7
Seal, Sheila, Thompson, Deborah, ... Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 38, No. 11 (2006), p. 1239-1241
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2006
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8
Douglas, Jenny, Cilliers, Deirdre, ... Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 8 (2007), p. 963-965
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2007
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9
Rahman, Nazneen, Seal, Sheila, ... PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 2 (2007), p. 165-167
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2007
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10
Reid, Sarah, Schindler, Detlev, ... Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 2 (2007), p. 162-164
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2007
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11
Meijers-Heijboer, Hanne, van den Ouweland, Ans, ... Low-penetrance susceptibility to breast cancer due to CHEK2<sup>*</sup>1100delC in noncarriers of BRCA1 or BRCA2 mutations
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 31, No. 1 (2002), p. 55-59
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2002
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12
Cox, Angela, Dunning, Alison M, ... Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 5 (2007), p. 688-688
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2007
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13
Cox, Angela, Dunning, Alison M, ... A common coding variant in CASP8 is associated with breast cancer risk
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 3 (2007), p. 352-358
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2007
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14
Burton, Paul R, Clayton, David G, ... Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 11 (2007), p. 1329-1337
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2007
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15
Nejentsev, Sergey, Howson, Joanna M. M., ... Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 450, No. 7171 (2007), p. 887-892
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2007
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16
Easton, Douglas F., Pooley, Karen A., ... Genome-wide association study identifies novel breast cancer susceptibility loci
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 447, No. 7148 (2007), p. 1087-1093
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2007
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17
Burton, Paul R., Clayton, David G., ... Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 447, No. 7145 (2007), p. 661-678
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2007