Works by Rahman, Nazneen

Results: 65

Insights into BRCA Cancer Predisposition from Integrated Germline and Somatic Analyses in 7632 Cancers.

Published in:

JNCI Cancer Spectrum, 2019, v. 3, n. 2, p. N.PAG, doi. 10.1093/jncics/pkz028

By:

Yost, Shawn;
Ruark, Elise;
Alexandrov, Ludmil B;
Rahman, Nazneen

Publication type:

Article

Aneuploidy-Cancer Predisposition Syndromes.

Published in:

Cell Cycle, 2005, v. 4, n. 2, p. 225, doi. 10.4161/cc.4.2.1419

By:

Hanks, Sandra;
Rahman, Nazneen

Publication type:

Article

Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23‐q24.

Published in:

Annals of Neurology, 2005, v. 57, n. 2, p. 293

By:

Meriel E. McEntagart;
Sarah L. Reid;
Alexandre Irtthum;
Jenny B. Douglas;
Keith E. D. Eyre;
Michael J. Donaghy;
Neil E. Anderson;
Nazneen Rahman

Publication type:

Article

Chromosomal instability by mutations in the novel minor spliceosome component CENATAC.

Published in:

EMBO Journal, 2021, v. 40, n. 14, p. 1, doi. 10.15252/embj.2020106536

By:

Wolf, Bas;
Oghabian, Ali;
Akinyi, Maureen V;
Hanks, Sandra;
Tromer, Eelco C;
Hooff, Jolien J E;
Voorthuijsen, Lisa;
Rooijen, Laura E;
Verbeeren, Jens;
Uijttewaal, Esther C H;
Baltissen, Marijke P A;
Yost, Shawn;
Piloquet, Philippe;
Vermeulen, Michiel;
Snel, Berend;
Isidor, Bertrand;
Rahman, Nazneen;
Frilander, Mikko J;
Kops, Geert J P L

Publication type:

Article

Antioxidant and anti-inflammatory potentials of Solanum pubescens Willd an ethnomedicinal plant of South Western Andhra Pradesh, India.

Published in:

Journal of Research in Pharmacy, 2019, v. 23, n. 2, p. 187, doi. 10.12991/jrp.2019.124

By:

RAHMAN, Haseebur;
RAHMAN, Nazneen;
HARIS, Mir;
MAHMOOD, Riaz

Publication type:

Article

Antioxidant, anti-inflammatory and wound healing properties of ethanolic extracts of Thevetia peruviana (Pers.) K. Schum.

Published in:

Journal of Research in Pharmacy, 2019, v. 23, n. 1, p. 101, doi. 10.12991/jrp.2018.114

By:

RAHMAN, Nazneen;
RAHMAN, Haseebur;
HARIS, Mir;
MAHMOOD, Riaz

Publication type:

Article

Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.

Published in:

JAMA Network Open, 2019, v. 2, n. 5, p. e194428, doi. 10.1001/jamanetworkopen.2019.4428

By:

Kemp, Zoe;
Turnbull, Alice;
Yost, Shawn;
Seal, Sheila;
Mahamdallie, Shazia;
Poyastro-Pearson, Emma;
Warren-Perry, Margaret;
Eccleston, Anthony;
Tan, Min-Min;
Teo, Soo Hwang;
Turner, Nicholas;
Strydom, Ann;
George, Angela;
Rahman, Nazneen

Publication type:

Article

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.

Published in:

Oncogene, 2000, v. 19, n. 36, p. 4170, doi. 10.1038/sj.onc.1203735

By:

Rahman, Nazneen;
Teare, M Dawn;
Seal, Sheila;
Renard, Helene;
Mangion, Jon;
Cour, Chantal;
Thompson, Deborah;
Shugart, Yin;
Eccles, Diana;
Devilee, Peter;
Meijers, Hanne;
Nathanson, Katherine L;
Neuhausen, Susan L;
Weber, Barbara;
Chang-Claude, Jenny;
Easton, Douglas F;
Goldgar, David;
Stratton, Michael R

Publication type:

Article

Corrigendum: Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.

Published in:

Human Molecular Genetics, 2019, v. 28, n. 9, p. 1578, doi. 10.1093/hmg/ddy424

By:

Loveday, Chey;
Tatton-Brown, Katrina;
Clarke, Matthew;
Westwood, Isaac;
Renwick, Anthony;
Ramsay, Emma;
Nemeth, Andrea;
Campbell, Jennifer;
Joss, Shelagh;
Gardner, McKinlay;
Zachariou, Anna;
Elliott, Anna;
Ruark, Elise;
Montfort, Rob van;
Rahman, Nazneen

Publication type:

Article

Evaluation of RAD50 in familial breast cancer predisposition.

Published in:

International Journal of Cancer, 2006, v. 118, n. 11, p. 2911, doi. 10.1002/ijc.21738

By:

Tommiska, Johanna;
Seal, Sheila;
Renwick, Anthony;
Barfoot, Rita;
Baskcomb, Linda;
Jayatilake, Hiran;
Bartkova, Jirina;
Tallila, Jonna;
Kaare, Milja;
Tamminen, Anitta;
Heikkilä, Päivi;
Evans, D. Gareth;
Eccles, Diana;
Aittomäki, Kristiina;
Blomqvist, Carl;
Bartek, Jiri;
Stratton, Michael R.;
Nevanlinna, Heli;
Rahman, Nazneen

Publication type:

Article

Periodontal treatment of two siblings with juvenile hyaline fibromatosis.

Published in:

Journal of Clinical Periodontology, 2005, v. 32, n. 9, p. 1016, doi. 10.1111/j.1600-051X.2005.00760.x

By:

Hakki, Sema S.;
Ataoglu, Tamer;
Avunduk, Mustafa C.;
Erdemli, Esra;
Gunhan, Omer;
Rahman, Nazneen

Publication type:

Article

The emerging landscape of breast cancer susceptibility.

Published in:

Nature Genetics, 2008, v. 40, n. 1, p. 17, doi. 10.1038/ng.2007.53

By:

Stratton, Michael R.;
Rahman, Nazneen

Publication type:

Article

Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 963, doi. 10.1038/ng2083

By:

Douglas, Jenny;
Cilliers, Deirdre;
Coleman, Kim;
Tatton-Brown, Katrina;
Barker, Karen;
Bernhard, Brigitte;
Burn, John;
Huson, Susan;
Josifova, Dragana;
Lacombe, Didier;
Malik, Mohsin;
Mansour, Sahar;
Reid, Evan;
Cormier-Daire, Valerie;
Cole, Trevor;
Rahman, Nazneen

Publication type:

Article

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 162, doi. 10.1038/ng1947

By:

Reid, Sarah;
Schindler, Detlev;
Hanenberg, Helmut;
Barker, Karen;
Hanks, Sandra;
Kalb, Reinhard;
Neveling, Kornelia;
Kelly, Patrick;
Seal, Sheila;
Freund, Marcel;
Wurm, Melanie;
Batish, Sat Dev;
Lach, Francis P.;
Yetgin, Sevgi;
Neitzel, Heidemarie;
Ariffin, Hany;
Tischkowitz, Marc;
Mathew, Christopher G.;
Auerbach, Arleen D.;
Rahman, Nazneen

Publication type:

Article

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 165, doi. 10.1038/ng1959

By:

Rahman, Nazneen;
Seal, Sheila;
Thompson, Deborah;
Kelly, Patrick;
Renwick, Anthony;
Elliott, Anna;
Reid, Sarah;
Spanova, Katarina;
Barfoot, Rita;
Chagtai, Tasnim;
Jayatilake, Hiran;
McGuffog, Lesley;
Hanks, Sandra;
Evans, D. Gareth;
Eccles, Diana;
Easton, Douglas F.;
Stratton, Michael R.

Publication type:

Article

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles.

Published in:

Nature Genetics, 2006, v. 38, n. 11, p. 1239, doi. 10.1038/ng1902

By:

Seal, Sheila;
Thompson, Deborah;
Renwick, Anthony;
Elliott, Anna;
Kelly, Patrick;
Barfoot, Rita;
Chagtai, Tasnim;
Jayatilake, Hiran;
Ahmed, Munaza;
Spanova, Katarina;
North, Bernard;
McGuffog, Lesley;
Evans, D. Gareth;
Eccles, Diana;
Easton, Douglas F.;
Stratton, Michael R.;
Rahman, Nazneen

Publication type:

Article

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.

Published in:

Nature Genetics, 2006, v. 38, n. 8, p. 873, doi. 10.1038/ng1837

By:

Renwick, Anthony;
Thompson, Deborah;
Seal, Sheila;
Kelly, Patrick;
Chagtai, Tasnim;
Ahmed, Munaza;
North, Bernard;
Jayatilake, Hiran;
Barfoot, Rita;
Spanova, Katarina;
McGuffog, Lesley;
Evans, D. Gareth;
Eccles, Diana;
Easton, Douglas F.;
Stratton, Michael R.;
Rahman, Nazneen

Publication type:

Article

A new gene on the X involved in Fanconi anemia.

Published in:

Nature Genetics, 2004, v. 36, n. 11, p. 1142, doi. 10.1038/ng1104-1142

By:

Rahman, Nazneen;
Ashworth, Alan

Publication type:

Article

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.

Published in:

Nature Genetics, 2004, v. 36, n. 11, p. 1159, doi. 10.1038/ng1449

By:

Hanks, Sandra;
Coleman, Kim;
Reid, Sarah;
Plaja, Alberto;
Firth, Helen;
FitzPatrick, David;
Kidd, Alexa;
Méhes, Károly;
Nash, Richard;
Robin, Nathanial;
Shannon, Nora;
Tolmie, John;
Swansbury, John;
Irrthum, Alexandre;
Douglas, Jenny;
Rahman, Nazneen

Publication type:

Article

A census of human cancer genes.

Published in:

Nature Reviews Cancer, 2004, v. 4, n. 3, p. 177, doi. 10.1038/nrc1299

By:

Futreal, P. Andrew;
Coin, Lachlan;
Marshall, Mhairi;
Down, Thomas;
Hubbard, Timothy;
Wooster, Richard;
Rahman, Nazneen;
Stratton, Michael R.

Publication type:

Article

Recognition of and Response to neonatal intrapartum-related complications in home-birth settings in Bangladesh.

Published in:

2014

By:

VanderEnde, Kristin E;
Moran, Allisyn C;
Leasure, Karen;
Day, Louise T;
Afsana, Kaosar;
Kalim, Nahid;
Munira, Shirajum;
Rahman, Nazneen;
Islam, Munia;
Khan, Jasmin;
Sibley, Lynn M

Publication type:

journal article

Recognition of and Response to Neonatal Intrapartum-related Complications in Home-birth Settings in Bangladesh.

Published in:

Journal of Health, Population & Nutrition, 2014, v. 32, n. 3, p. 503

By:

VanderEnde, Kristin E.;
Moran, Allisyn C.;
Leasure, Karen;
Day, Louise T.;
Afsana, Kaosar;
Kalim, Nahid;
Munira, Shirajum;
Rahman, Nazneen;
Islam, Munia;
Khan, Jasmin;
Sibley, Lynn M.

Publication type:

Article

Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma.

Published in:

PLoS Genetics, 2017, v. 13, n. 5, p. 1, doi. 10.1371/journal.pgen.1006787

By:

McDaniel, Lee D.;
Conkrite, Karina L.;
Chang, Xiao;
Capasso, Mario;
Vaksman, Zalman;
Oldridge, Derek A.;
Zachariou, Anna;
Horn, Millicent;
Diamond, Maura;
Huo, Cuiping;
Iolascon, Achille;
Hakonarson, Hakon;
Rahman, Nazneen;
Devoto, Marcella;
Diskin, Sharon J.

Publication type:

Article

Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma.

Published in:

Familial Cancer, 2011, v. 10, n. 2, p. 337, doi. 10.1007/s10689-010-9411-0

By:

Slade, Ingrid;
Murray, Anne;
Hanks, Sandra;
Kumar, Ajith;
Walker, Lisa;
Hargrave, Darren;
Douglas, Jenny;
Stiller, Charles;
Izatt, Louise;
Rahman, Nazneen

Publication type:

Article

A new familial cancer syndrome including predisposition to Wilms tumor and neuroblastoma.

Published in:

Familial Cancer, 2010, v. 9, n. 3, p. 425, doi. 10.1007/s10689-009-9319-8

By:

Abbaszadeh, Fatemeh;
Barker, Karen;
McConville, Carmel;
Scott, Richard;
Rahman, Nazneen

Publication type:

Article

Simple Detection of Germline Microsatellite Instability for Diagnosis of Constitutional Mismatch Repair Cancer Syndrome.

Published in:

Human Mutation, 2013, v. 34, n. 6, p. 847, doi. 10.1002/humu.22311

By:

Ingham, Danielle;
Diggle, Christine P.;
Berry, Ian;
Bristow, Claire A.;
Hayward, Bruce E.;
Rahman, Nazneen;
Markham, Alexander F.;
Sheridan, Eamonn G.;
Bonthron, David T.;
Carr, Ian M.

Publication type:

Article

Corrigendum: Realizing the promise of cancer predisposition genes.

Published in:

Nature, 2014, v. 510, n. 7503, p. 176, doi. 10.1038/nature13431

By:

Rahman, Nazneen

Publication type:

Article

Realizing the promise of cancer predisposition genes.

Published in:

Nature, 2014, v. 505, n. 7483, p. 302, doi. 10.1038/nature12981

By:

Rahman, Nazneen

Publication type:

Article

Penetrance of mutations in the familial Wilms tumor gene FWT1.

Published in:

2000

By:

Rahman, Nazneen;
Arbour, Laura;
Rahman, N;
Arbour, L;
Houlston, R;
Bonaïti-Pellié, C;
Abidi, F;
Tranchemontagne, J;
Ford, D;
Narod, S;
Pritchard-Jones, K;
Foulkes, W D;
Schwartz, C;
Stratton, M R

Publication type:

journal article

Prevalence of BRCA1 and BRCA2 gene mutations in patients with early-onset breast cancer.

Published in:

1999

By:

Peto, Julian;
Collins, Nadine;
Barfoot, Rita;
Seal, Sheila;
Warren, William;
Rahman, Nazneen;
Easton, Douglas F.;
Evans, Christopher;
Deacon, Judith;
Stratton, Michael R.;
Peto, J;
Collins, N;
Barfoot, R;
Seal, S;
Warren, W;
Rahman, N;
Easton, D F;
Evans, C;
Deacon, J;
Stratton, M R

Publication type:

journal article

Oncologist-led BRCA 'mainstreaming' in the ovarian cancer clinic: A study of 255 patients and its impact on their management.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-60149-5

By:

Rumford, Megan;
Lythgoe, Mark;
McNeish, Iain;
Gabra, Hani;
Tookman, Laura;
Rahman, Nazneen;
George, Angela;
Krell, Jonathan

Publication type:

Article

MCF classifier: Estimating, standardizing, and stratifying medicine carbon footprints, at scale.

Published in:

British Journal of Clinical Pharmacology, 2024, v. 90, n. 11, p. 2713, doi. 10.1111/bcp.16229

By:

Taylor, Haroon;
Mahamdallie, Shazia;
Sawyer, Matthew;
Rahman, Nazneen

Publication type:

Article

The NSD1 and EZH2 overgrowth genes, similarities and differences.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 2, p. 1, doi. 10.1002/ajmg.c.31359

By:

TATTON‐BROWN, KATRINA;
RAHMAN, NAZNEEN

Publication type:

Article

The familial Wilms' tumour susceptibility gene, FWT1, may not be a tumour suppressor gene.

Published in:

Oncogene, 1997, v. 14, n. 25, p. 3099, doi. 10.1038/sj.onc.1201107

By:

Rahman, Nazneen;
Arbour, Laura;
Tonin, Patricia;
Baruchel, Sylvain;
Pritchard-Jones, Kathryn;
Narod, Steven A;
Stratton, Michael R

Publication type:

Article

Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour.

Published in:

Nature Communications, 2014, v. 5, n. 8, p. 4398, doi. 10.1038/ncomms5398

By:

Hanks, Sandra;
Perdeaux, Elizabeth R.;
Seal, Sheila;
Ruark, Elise;
Mahamdallie, Shazia S.;
Murray, Anne;
Ramsay, Emma;
Del Vecchio Duarte, Silvana;
Zachariou, Anna;
de Souza, Bianca;
Warren-Perry, Margaret;
Elliott, Anna;
Davidson, Alan;
Price, Helen;
Stiller, Charles;
Pritchard-Jones, Kathy;
Rahman, Nazneen

Publication type:

Article

Sotos syndrome.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 3, p. 264, doi. 10.1038/sj.ejhg.5201686

By:

Tatton-Brown, Katrina;
Rahman, Nazneen

Publication type:

Article

Evaluation of NSD2 and NSD3 in overgrowth syndromes.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 2, p. 150, doi. 10.1038/sj.ejhg.5201298

By:

Douglas, Jenny;
Coleman, Kim;
Tatton-Brown, Katrina;
Hughes, Helen E;
Temple, I Karen;
Cole, Trevor R. P;
Rahman, Nazneen

Publication type:

Article

OpEx - a validated, automated pipeline optimised for clinical exome sequence analysis.

Published in:

Scientific Reports, 2016, p. 31029, doi. 10.1038/srep31029

By:

Ruark, Elise;
Münz, Márton;
Clarke, Matthew;
Renwick, Anthony;
Ramsay, Emma;
Elliott, Anna;
Seal, Sheila;
Lunter, Gerton;
Rahman, Nazneen

Publication type:

Article

Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients.

Published in:

Scientific Reports, 2016, p. 29506, doi. 10.1038/srep29506

By:

George, Angela;
Riddell, Daniel;
Seal, Sheila;
Talukdar, Sabrina;
Mahamdallie, Shazia;
Ruark, Elise;
Cloke, Victoria;
Slade, Ingrid;
Kemp, Zoe;
Gore, Martin;
Strydom, Ann;
Banerjee, Susana;
Hanson, Helen;
Rahman, Nazneen

Publication type:

Article

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 17, p. 4775, doi. 10.1093/hmg/ddv182

By:

Loveday, Chey;
Tatton-Brown, Katrina;
Clarke, Matthew;
Westwood, Isaac;
Renwick, Anthony;
Ramsay, Emma;
Nemeth, Andrea;
Campbell, Jennifer;
Joss, Shelagh;
Gardner, McKinlay;
Zachariou, Anna;
Elliott, Anna;
Ruark, Elise;
van Montfort, Rob;
Rahman, Nazneen

Publication type:

Article

Multi-stage genome-wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 4, p. 1169, doi. 10.1093/hmg/ddu511

By:

Litchfield, Kevin;
Sultana, Razvan;
Renwick, Anthony;
Dudakia, Darshna;
Seal, Sheila;
Ramsay, Emma;
Powell, Silvana;
Elliott, Anna;
Warren-Perry, Margaret;
Eeles, Rosalind;
Peto, Julian;
Kote-Jarai, Zsofia;
Muir, Kenneth;
Nsengimana, Jeremie;
Stratton, Michael R.;
Easton, Douglas F.;
Bishop, D. Timothy;
Huddart, Robert A.;
Rahman, Nazneen;
Turnbull, Clare

Publication type:

Article

Pathway-based analysis of GWAs data identifies association of sex determination genes with susceptibility to testicular germ cell tumors.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 22, p. 6061, doi. 10.1093/hmg/ddu305

By:

Koster, Roelof;
Mitra, Nandita;
D'Andrea, Kurt;
Vardhanabhuti, Saran;
Chung, Charles C.;
Wang, Zhaoming;
Loren Erickson, R.;
Vaughn, David J.;
Litchfield, Kevin;
Rahman, Nazneen;
Greene, Mark H.;
McGlynn, Katherine A.;
Turnbull, Clare;
Chanock, Stephen J.;
Nathanson, Katherine L.;
Kanetsky, Peter A.

Publication type:

Article

Cancer genes associated with phenotypes in monoallelic and biallelic mutation carriers: new lessons from old players.

Published in:

Human Molecular Genetics, 2007, v. 16, n. R1, p. R60, doi. 10.1093/hmg/ddm026

By:

Rahman, Nazneen;
Scott, Richard H.

Publication type:

Article

Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.

Published in:

Kidney International, 2003, v. 64, n. 5, p. 1580, doi. 10.1046/j.1523-1755.2003.00269.x

By:

Wolf, Matthias T.F.;
Mucha, Bettina E.;
Attanasio, Massimo;
Zalewski, Isabella;
Karle, Stephanie M.;
Neumann, Hartmut P.H.;
Rahman, Nazneen;
Bader, Birgit;
Baldamus, Conrad A.;
Otto, Edgar;
Witzgall, Ralph;
Fuchshuber, Arno;
Hildebrandt, Friedhelm

Publication type:

Article

Confirmation of a gene locus for medullary cystic kidney disease (MCKD2) on chromosome 16p12.

Published in:

Kidney International, 2001, v. 60, n. 4, p. 1233, doi. 10.1046/j.1523-1755.2001.00932.x

By:

Hateboer, Nick;
Gumbs, Curtis;
Teare, M. Dawn;
Coles, Gerry A.;
Griffiths, David;
Ravine, David;
Futreal, P. Andrew;
Rahman, Nazneen

Publication type:

Article

The integration of BRCA testing into oncology clinics.

Published in:

British Journal of Nursing, 2016, v. 25, n. 12, p. 690, doi. 10.12968/bjon.2016.25.12.690

By:

Percival, Natalie;
George, Angela;
Gyertson, Jennifer;
Hamill, Monica;
Fernandes, Andreia;
Davies, Emily;
Rahman, Nazneen;
Banerjee, Susana

Publication type:

Article

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinical setting.

Published in:

Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0195-6

By:

Münz, Márton;
Ruark, Elise;
Renwick, Anthony;
Ramsay, Emma;
Clarke, Matthew;
Mahamdallie, Shazia;
Cloke, Victoria;
Seal, Sheila;
Strydom, Ann;
Lunter, Gerton;
Rahman, Nazneen

Publication type:

Article

Development of cancer genetic services in the UK: A national consultation.

Published in:

Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0128-4

By:

Slade, Ingrid;
Riddell, Daniel;
Turnbull, Clare;
Hanson, Helen;
Rahman, Nazneen

Publication type:

Article

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.

Published in:

Nature Genetics, 2015, v. 47, n. 4, p. 373, doi. 10.1038/ng.3242

By:

Michailidou, Kyriaki;
Dennis, Joe;
Lush, Michael J;
Bolla, Manjeet K;
Wang, Qin;
Rahman, Nazneen;
Turnbull, Clare;
Schoemaker, Minouk J;
Muir, Kenneth;
Lophatananon, Artitaya;
Stewart-Brown, Sarah;
Siriwanarangsan, Pornthep;
Hartman, Mikael;
Miao, Hui;
Chia, Kee Seng;
Chan, Ching Wan;
Fasching, Peter A;
Hein, Alexander;
Beckmann, Matthias W;
Haeberle, Lothar

Publication type:

Article

Meta-analysis identifies four new loci associated with testicular germ cell tumor.

Published in:

Nature Genetics, 2013, v. 45, n. 6, p. 680, doi. 10.1038/ng.2634

By:

Chung, Charles C;
Kanetsky, Peter A;
Wang, Zhaoming;
Hildebrandt, Michelle A T;
Koster, Roelof;
Skotheim, Rolf I;
Kratz, Christian P;
Turnbull, Clare;
Cortessis, Victoria K;
Bakken, Anne C;
Bishop, D Timothy;
Cook, Michael B;
Erickson, R Loren;
Fosså, Sophie D;
Jacobs, Kevin B;
Korde, Larissa A;
Kraggerud, Sigrid M;
Lothe, Ragnhild A;
Loud, Jennifer T;
Rahman, Nazneen

Publication type:

Article