Abramsky, L; Hall, S; Levitan, J; Marteau, TM; Fletcher, O; (2002) Communicating with parents about fetal abnormality. [Conference or Workshop Item] https://researchonline.lshtm.ac.uk/id/eprint/17419 Full text not available from this repository.

Antoniou, AC; Pharoah, PD; Narod, S; Risch, HA; Eyfjord, JE; Hopper, JL; Olsson, H; Johannsson, O; Borg, A; Pasini, B; +22 more... Radice, P; Manoukian, S; Eccles, DM; Tang, N; Olah, E; Anton-Culver, H; Warner, E; Lubinski, J; Gronwald, J; Gorski, B; Tulinius, H; Thorlacius, S; Eerola, H; Nevanlinna, H; Syrjäkoski, K; Kallioniemi, OP; Thompson, D; Evans, C; Peto, J; Lalloo, F; Evans, DG; Easton, DF; (2005) Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies. Journal of medical genetics, 42 (7). pp. 602-3. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2004.024133 Full text not available from this repository.

Apostolidou, S; Abu-Amero, S; O'Donoghue, K; Olafsdottir, O; Chavele, KM; Frost, J; Whittaker, JC; Loughna, P; Stanier, P; Moore, GE; (2006) Elevated maternal expression of the imprinted PHLDA2 gene is associated with low birth weight. [Conference or Workshop Item] https://researchonline.lshtm.ac.uk/id/eprint/9687 Full text not available from this repository.

Dawes, R; Hennig, B; Irving, W; Petrova, S; Boxall, S; Ward, V; Wallace, D; Macallan, DC; Thursz, M; Hill, A; +3 more... Bodmer, W; Beverley, PC; Tchilian, EZ; (2006) Altered CD45 expression in C77G carriers influences immune function and outcome of hepatitis C infection. Journal of medical genetics, 43 (8). pp. 678-84. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2005.040485 Full text not available from this repository.

Khor, CC; Davila, S; Shimizu, C; Sheng, S; Matsubara, T; Suzuki, Y; Newburger, JW; Baker, A; Burgner, D; Breunis, W; +6 more... Kuijpers, T; Wright, VJ; Levin, M; Hibberd, ML; Burns, JC; US and International Kawasaki Disease Genetics Consortia; (2011) Genome-wide linkage and association mapping identify susceptibility alleles in ABCC4 for Kawasaki disease. Journal of medical genetics, 48 (7). pp. 467-72. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2010.086611 Full text not available from this repository.

MacDermot, KD; Holmes, A; Miners, AH; (2001) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. Journal of medical genetics, 38 (11). pp. 769-75. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.38.11.769 Full text not available from this repository.

MacDermot, KD; Holmes, A; Miners, AH; (2001) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. Journal of medical genetics, 38 (11). pp. 750-60. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.38.11.750 Full text not available from this repository.

Manchanda, R; Burnell, M; Loggenberg, K; Desai, R; Wardle, J; Sanderson, SC; Gessler, S; Side, L; Balogun, N; Kumar, A; +12 more... Dorkins, H; Wallis, Y; Chapman, C; Tomlinson, I; Taylor, R; Jacobs, C; Legood, R; Raikou, M; McGuire, A; Beller, U; Menon, U; Jacobs, I; (2016) Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations. Journal of medical genetics, 53 (7). pp. 472-80. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2015-103740 Full text not available from this repository.

Milne, RL; Lorenzo-Bermejo, J; Burwinkel, B; Malats, N; Arias, JI; Zamora, MP; Benitez, J; Humphreys, MK; Garcia-Closas, M; Chanock, SJ; +74 more... Lissowska, J; Sherman, ME; Mannermaa, A; Kataja, V; Kosma, VM; Nevanlinna, H; Heikkinen, T; Aittomaki, K; Blomqvist, C; Anton-Culver, H; Ziogas, A; Devilee, P; van Asperen, CJ; Tollenaar, R; Seynaeve, C; Hall, P; Czene, K; Liu, JJ; Irwanto, AK; Kang, D; Yoo, KY; Noh, DY; Couch, FJ; Olson, JE; Wang, XS; Fredericksen, Z; Nordestgaard, BG; Bojesen, SE; Flyger, H; Margolin, S; Lindblom, A; Fasching, PA; Schulz-Wendtland, R; Ekici, AB; Beckmann, MW; Wang-Gohrke, S; Shen, CY; Yu, JC; Hsu, HM; Wu, PE; Giles, GG; Severi, G; Baglietto, L; English, DR; Cox, A; Brock, I; Elliott, G; Reed, MWR; Beesley, J; Chen, XQ; Fletcher, O; Gibson, L; Silva, ID; Peto, J; Frank, B; Heil, J; Meindl, A; Chang-Claude, J; Hein, R; Vrieling, A; Flesch-Janys, D; Southey, MC; Smith, L; Apicella, C; Hopper, JL; Dunning, AM; Pooley, KA; Pharoah, PDP; Hamann, U; Pesch, B; Ko, YD; Easton, DF; Chenevix-Trench, G; Network, KCIAGG; (2011) 7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium. Journal of medical genetics, 48 (10). pp. 698-702. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2011-100303 Full text not available from this repository.

Parra, EJ; Hoggart, CJ; Bonilla, C; Dios, S; Norris, JM; Marshall, JA; Hamman, RF; Ferrell, RE; McKeigue, PM; Shriver, MD; (2004) Relation of type 2 diabetes to individual admixture and candidate gene polymorphisms in the Hispanic American population of San Luis Valley, Colorado. Journal of medical genetics, 41 (11). art. no.. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2004.018887 Full text not available from this repository.

Wozniak, MA; Faragher, EB; Todd, JA; Koram, KA; Riley, EM; Itzhaki, RF; (2003) Does apolipoprotein E polymorphism influence susceptibility to malaria? Journal of medical genetics, 40 (5). pp. 348-351. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.40.5.348 Full text not available from this repository.

Wozniak, MA; Riley, EM; Itzhaki, RF; (2004) Apolipoprotein E polymorphisms and risk of malaria. Journal of medical genetics, 41 (3). pp. 145-6. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2003.014613 Full text not available from this repository.

Fulford, AJ; Ong, KK; Elks, CE; Prentice, AM; Hennig, BJ; (2015) Progressive influence of body mass index-associated genetic markers in rural Gambians. Journal of medical genetics, 52 (6). pp. 375-80. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2014-102784

Manchanda, R; Blyuss, O; Gaba, F; Gordeev, VS; Jacobs, C; Burnell, M; Gan, C; Taylor, R; Turnbull, C; Legood, R; +4 more... Zaikin, A; Antoniou, AC; Menon, U; Jacobs, I; (2018) Current detection rates and time-to-detection of all identifiable BRCA carriers in the Greater London population. Journal of medical genetics, 55 (8). pp. 538-545. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2017-105195

Manchanda, R; Legood, R; Antoniou, AC; Gordeev, VS; Menon, U; (2016) Specifying the ovarian cancer risk threshold of 'premenopausal risk-reducing salpingo-oophorectomy' for ovarian cancer prevention: a cost-effectiveness analysis. Journal of medical genetics, 53 (9). pp. 591-9. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2016-103800

Southey, MC; Goldgar, DE; Winqvist, R; Pylkäs, K; Couch, F; Tischkowitz, M; Foulkes, WD; Dennis, J; Michailidou, K; van Rensburg, EJ; +318 more... Heikkinen, T; Nevanlinna, H; Hopper, JL; Dörk, T; Claes, KB; Reis-Filho, J; Teo, ZL; Radice, P; Catucci, I; Peterlongo, P; Tsimiklis, H; Odefrey, FA; Dowty, JG; Schmidt, MK; Broeks, A; Hogervorst, FB; Verhoef, S; Carpenter, J; Clarke, C; Scott, RJ; Fasching, PA; Haeberle, L; Ekici, AB; Beckmann, MW; Peto, J; Dos-Santos-Silva, I; Fletcher, O; Johnson, N; Bolla, MK; Sawyer, EJ; Tomlinson, I; Kerin, MJ; Miller, N; Marme, F; Burwinkel, B; Yang, R; Guénel, P; Truong, T; Menegaux, F; Sanchez, M; Bojesen, S; Nielsen, SF; Flyger, H; Benitez, J; Zamora, MP; Perez, JI; Menéndez, P; Anton-Culver, H; Neuhausen, S; Ziogas, A; Clarke, CA; Brenner, H; Arndt, V; Stegmaier, C; Brauch, H; Brüning, T; Ko, YD; Muranen, TA; Aittomäki, K; Blomqvist, C; Bogdanova, NV; Antonenkova, NN; Lindblom, A; Margolin, S; Mannermaa, A; Kataja, V; Kosma, VM; Hartikainen, JM; Spurdle, AB; Investigators, K; Australian Ovarian Cancer Study Group; Wauters, E; Smeets, D; Beuselinck, B; Floris, G; Chang-Claude, J; Rudolph, A; Seibold, P; Flesch-Janys, D; Olson, JE; Vachon, C; Pankratz, VS; McLean, C; Haiman, CA; Henderson, BE; Schumacher, F; Le Marchand, L; Kristensen, V; Alnæs, GG; Zheng, W; Hunter, DJ; Lindstrom, S; Hankinson, SE; Kraft, P; Andrulis, I; Knight, JA; Glendon, G; Mulligan, AM; Jukkola-Vuorinen, A; Grip, M; Kauppila, S; Devilee, P; Tollenaar, RA; Seynaeve, C; Hollestelle, A; Garcia-Closas, M; Figueroa, J; Chanock, SJ; Lissowska, J; Czene, K; Darabi, H; Eriksson, M; Eccles, DM; Rafiq, S; Tapper, WJ; Gerty, SM; Hooning, MJ; Martens, JW; Collée, JM; Tilanus-Linthorst, M; Hall, P; Li, J; Brand, JS; Humphreys, K; Cox, A; Reed, MW; Luccarini, C; Baynes, C; Dunning, AM; Hamann, U; Torres, D; Ulmer, HU; Rüdiger, T; Jakubowska, A; Lubinski, J; Jaworska, K; Durda, K; Slager, S; Toland, AE; Ambrosone, CB; Yannoukakos, D; Swerdlow, A; Ashworth, A; Orr, N; Jones, M; González-Neira, A; Pita, G; Alonso, MR; Álvarez, N; Herrero, D; Tessier, DC; Vincent, D; Bacot, F; Simard, J; Dumont, M; Soucy, P; Eeles, R; Muir, K; Wiklund, F; Gronberg, H; Schleutker, J; Nordestgaard, BG; Weischer, M; Travis, RC; Neal, D; Donovan, JL; Hamdy, FC; Khaw, KT; Stanford, JL; Blot, WJ; Thibodeau, S; Schaid, DJ; Kelley, JL; Maier, C; Kibel, AS; Cybulski, C; Cannon-Albright, L; Butterbach, K; Park, J; Kaneva, R; Batra, J; Teixeira, MR; Kote-Jarai, Z; Olama, AA; Benlloch, S; Renner, SP; Hartmann, A; Hein, A; Ruebner, M; Lambrechts, D; Van Nieuwenhuysen, E; Vergote, I; Lambretchs, S; Doherty, JA; Rossing, MA; Nickels, S; Eilber, U; Wang-Gohrke, S; Odunsi, K; Sucheston-Campbell, LE; Friel, G; Lurie, G; Killeen, JL; Wilkens, LR; Goodman, MT; Runnebaum, I; Hillemanns, PA; Pelttari, LM; Butzow, R; Modugno, F; Edwards, RP; Ness, RB; Moysich, KB; du Bois, A; Heitz, F; Harter, P; Kommoss, S; Karlan, BY; Walsh, C; Lester, J; Jensen, A; Kjaer, SK; Høgdall, E; Peissel, B; Bonanni, B; Bernard, L; Goode, EL; Fridley, BL; Vierkant, RA; Cunningham, JM; Larson, MC; Fogarty, ZC; Kalli, KR; Liang, D; Lu, KH; Hildebrandt, MA; Wu, X; Levine, DA; Dao, F; Bisogna, M; Berchuck, A; Iversen, ES; Marks, JR; Akushevich, L; Cramer, DW; Schildkraut, J; Terry, KL; Poole, EM; Stampfer, M; Tworoger, SS; Bandera, EV; Orlow, I; Olson, SH; Bjorge, L; Salvesen, HB; van Altena, AM; Aben, KK; Kiemeney, LA; Massuger, LF; Pejovic, T; Bean, Y; Brooks-Wilson, A; Kelemen, LE; Cook, LS; Le, ND; Górski, B; Gronwald, J; Menkiszak, J; Høgdall, CK; Lundvall, L; Nedergaard, L; Engelholm, SA; Dicks, E; Tyrer, J; Campbell, I; McNeish, I; Paul, J; Siddiqui, N; Glasspool, R; Whittemore, AS; Rothstein, JH; McGuire, V; Sieh, W; Cai, H; Shu, XO; Teten, RT; Sutphen, R; McLaughlin, JR; Narod, SA; Phelan, CM; Monteiro, AN; Fenstermacher, D; Lin, HY; Permuth, JB; Sellers, TA; Chen, YA; Tsai, YY; Chen, Z; Gentry-Maharaj, A; Gayther, SA; Ramus, SJ; Menon, U; Wu, AH; Pearce, CL; Van Den Berg, D; Pike, MC; Dansonka-Mieszkowska, A; Plisiecka-Halasa, J; Moes-Sosnowska, J; Kupryjanczyk, J; Pharoah, PD; Song, H; Winship, I; Chenevix-Trench, G; Giles, GG; Tavtigian, SV; Easton, DF; Milne, RL; (2016) PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. Journal of medical genetics, 53 (12). pp. 800-811. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmedgenet-2016-103839

Wellesley, D; Boyd, P; Dolk, H; Pattenden, S; (2005) An aetiological classification of birth defects for epidemiological research. Journal of medical genetics, 42 (1). pp. 54-7. ISSN 0022-2593 DOI: https://doi.org/10.1136/jmg.2004.023309