By Emeritus Professor Allan David Spigelman

Journal articles

Walker R; Joo JE; Mahmood K; Clendenning M; Como J; Preston SG; Joseland S; Pope BJ; Medeiros ABD; Murillo BV; Pachter N; Sweet K; Spigelman AD; Groves A; Gleeson M; Bernatowicz K; Poplawski N; Andrews L; Healey E; Gallinger S; Grant RC; Win AK; Hopper JL; Jenkins MA; Torrezan GT; Rosty C; Macrae FA; Winship IM; Buchanan DD; Georgeson P, 2025, 'Adenomas from individuals with pathogenic biallelic variants in the MUTYH and NTHL1 genes demonstrate base excision repair tumour mutational signature profiles similar to colorectal cancers, expanding potential diagnostic and variant classification applications', Translational Oncology, 52, http://dx.doi.org/10.1016/j.tranon.2024.102266

Chambers AJ; Enoch JF; Wong J; Spigelman A, 2024, 'When teams disagree: Investigating the incidence and causes of dissent occurring in cancer multidisciplinary team meetings', Asia Pacific Journal of Clinical Oncology, 20, pp. 234 - 239, http://dx.doi.org/10.1111/ajco.13919

Walker R; Mahmood K; Joo JE; Clendenning M; Georgeson P; Como J; Joseland S; Preston SG; Antill Y; Austin R; Boussioutas A; Bowman M; Burke J; Campbell A; Daneshvar S; Edwards E; Gleeson M; Goodwin A; Harris MT; Henderson A; Higgins M; Hopper JL; Hutchinson RA; Ip E; Isbister J; Kasem K; Marfan H; Milnes D; Ng A; Nichols C; O’Connell S; Pachter N; Pope BJ; Poplawski N; Ragunathan A; Smyth C; Spigelman A; Storey K; Susman R; Taylor JA; Warwick L; Wilding M; Williams R; Win AK; Walsh MD; Macrae FA; Jenkins MA; Rosty C; Winship IM; Buchanan DD, 2023, 'A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome', Journal of Translational Medicine, 21, http://dx.doi.org/10.1186/s12967-023-04143-1

Walker R; Mahmood K; Como J; Clendenning M; Joo JE; Georgeson P; Joseland S; Preston SG; Pope BJ; Chan JM; Austin R; Bojadzieva J; Campbell A; Edwards E; Gleeson M; Goodwin A; Harris MT; Ip E; Kirk J; Mansour J; Mar Fan H; Nichols C; Pachter N; Ragunathan A; Spigelman A; Susman R; Christie M; Jenkins MA; Pai RK; Rosty C; Macrae FA; Winship IM; Buchanan DD, 2023, 'DNA Mismatch Repair Gene Variant Classification: Evaluating the Utility of Somatic Mutations and Mismatch Repair Deficient Colonic Crypts and Endometrial Glands', Cancers, 15, http://dx.doi.org/10.3390/cancers15204925

Clarke J; Boussioutas A; Flanders B; Lockett T; Harrap K; Saunders I; Lynch P; Appleyard M; Spigelman A; Cameron D; Macrae F, 2023, 'Can butyrate prevent colon cancer? The AusFAP study: A randomised, crossover clinical trial', Contemporary Clinical Trials Communications, 32, http://dx.doi.org/10.1016/j.conctc.2023.101092

Ahearn TU; Zhang H; Michailidou K; Milne RL; Bolla MK; Dennis J; Dunning AM; Lush M; Wang Q; Andrulis IL; Anton-Culver H; Arndt V; Aronson KJ; Auer PL; Augustinsson A; Baten A; Becher H; Behrens S; Benitez J; Bermisheva M; Blomqvist C; Bojesen SE; Bonanni B; Børresen-Dale AL; Brauch H; Brenner H; Brooks-Wilson A; Brüning T; Burwinkel B; Buys SS; Canzian F; Castelao JE; Chang-Claude J; Chanock SJ; Chenevix-Trench G; Clarke CL; Sahlberg KK; Ottestad L; Kåresen R; Schlichting E; Holmen MM; Sauer T; Haakensen V; Engebråten O; Naume B; Fosså A; Kiserud CE; Reinertsen KV; Helland Å; Riis M; Geisler J; Collée JM; Cox A; Cross SS; Czene K; Daly MB; Devilee P; Dörk T; Dwek M; Eccles DM; Evans DG; Fasching PA; Figueroa J; Floris G; Gago-Dominguez M; Gapstur SM; García-Sáenz JA; Gaudet MM; Giles GG; Goldberg MS; González-Neira A; Alnæs GIG; Grip M; Guénel P; Haiman CA; Hall P; Hamann U; Harkness EF; Heemskerk-Gerritsen BAM; Holleczek B; Hollestelle A; Hooning MJ; Hoover RN; Hopper JL; Howell A; Balleine R; Baxter R; Braye S; Carpenter J; Dahlstrom J; Forbes J; Lee CS; Marsh D; Morey A; Pathmanathan N; Scott R; Simpson P; Spigelman A; Wilcken N, 2022, 'Common variants in breast cancer risk loci predispose to distinct tumor subtypes', Breast Cancer Research, 24, http://dx.doi.org/10.1186/s13058-021-01484-x

Wong-Brown M; McPhillips M; Gleeson M; Spigelman AD; Meldrum CJ; Dooley S; Scott RJ, 2022, 'Correction: When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans (Hereditary Cancer in Clinical Practice, (2016), 14, 1, (6), 10.1186/s13053-015-0045-y)', Hereditary Cancer in Clinical Practice, 20, http://dx.doi.org/10.1186/s13053-022-00228-y

Hallenstein LG; Sorensen C; Hodgson L; Wen S; Westhuyzen J; Hansen C; Last ATJ; Amalaseelan JV; Salindera S; Ross W; Spigelman AD; Shakespeare TP; Aherne NJ, 2021, 'Assessment of genetic referrals and outcomes for women with triple negative breast cancer in regional cancer centres in Australia', Hereditary Cancer in Clinical Practice, 19, http://dx.doi.org/10.1186/s13053-021-00176-z

Murali K; Dwarte TM; Nikfarjam M; Tucker KM; Vaughan RB; Efthymiou M; Collins A; Spigelman AD; Salmon L; Johns AL; Williams DB; Delatycki MB; John T; Stoita A, 2021, 'Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants (Hereditary Cancer in Clinical Practice, (2021), 19, 1, (33), 10.1186/s13053-021-00190-1)', Hereditary Cancer in Clinical Practice, 19, http://dx.doi.org/10.1186/s13053-021-00195-w

Bernstedt SW; Björk J; Fritzell K; Spigelman AD; Björck E; Backman AS, 2021, 'Room for improvement: One third of Lynch syndrome patients presenting for genetic testing in a highly specialised centre in Stockholm already have cancer', Hereditary Cancer in Clinical Practice, 19, pp. 18, http://dx.doi.org/10.1186/s13053-021-00171-4

Murali K; Dwarte TM; Nikfarjam M; Tucker KM; Vaughan RB; Efthymiou M; Collins A; Spigelman AD; Salmon L; Johns AL; Williams DB; Delatycki MB; John T; Stoita A, 2021, 'Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants', Hereditary Cancer in Clinical Practice, 19, http://dx.doi.org/10.1186/s13053-021-00190-1

Bancroft EK; Page EC; Brook MN; Thomas S; Taylor N; Pope J; McHugh J; Jones AB; Karlsson Q; Merson S; Ong KR; Hoffman J; Huber C; Maehle L; Grindedal EM; Stormorken A; Evans DG; Rothwell J; Lalloo F; Brady AF; Bartlett M; Snape K; Hanson H; James P; McKinley J; Mascarenhas L; Syngal S; Ukaegbu C; Side L; Thomas T; Barwell J; Teixeira MR; Izatt L; Suri M; Macrae FA; Poplawski N; Chen-Shtoyerman R; Ahmed M; Musgrave H; Nicolai N; Greenhalgh L; Brewer C; Pachter N; Spigelman AD; Azzabi A; Helfand BT; Halliday D; Buys S; Ramon y Cajal T; Donaldson A; Cooney KA; Harris M; McGrath J; Davidson R; Taylor A; Cooke P; Myhill K; Hogben M; Aaronson NK; Ardern-Jones A; Bangma CH; Castro E; Dearnaley D; Dias A; Dudderidge T; Eccles DM; Green K; Eyfjord J; Falconer A; Foster CS; Gronberg H; Hamdy FC; Johannsson O; Khoo V; Lilja H; Lindeman GJ; Lubinski J; Axcrona K; Mikropoulos C; Mitra AV; Moynihan C; Ni Raghallaigh H; Rennert G; Collier R; Adams L; Adlard J; Alfonso R; Ali S; Andrew A; Araújo L; Azam N; Ball D; Barker Q; Basevitch A; Benton B; Berlin C; Bermingham N; Biller L; Bloss A; Bradford M, 2021, 'A prospective prostate cancer screening programme for men with pathogenic variants in mismatch repair genes (IMPACT): initial results from an international prospective study', Lancet Oncology, 22, pp. 1618 - 1631, http://dx.doi.org/10.1016/S1470-2045(21)00522-2

Spigelman AD, 2021, 'The Spigelman Staging System for Duodenal Polyposis in Familial Adenomatous Polyposis: A Clarification From its Eponymous Author', Clinical Gastroenterology and Hepatology, 19, pp. 1735 - 1736, http://dx.doi.org/10.1016/j.cgh.2020.09.053

Win AK; Dowty JG; Reece JC; Lee G; Templeton AS; Plazzer JP; Buchanan DD; Akagi K; Aksoy S; Alonso A; Alvarez K; Amor DJ; Ankathil R; Aretz S; Arnold JL; Aronson M; Austin R; Backman AS; Bajwa-ten Broeke SW; Barca-Tierno V; Barwell J; Bernstein I; Berthet P; Betz B; Bignon YJ; Boisjoli T; Bonadona V; Briollais L; Brunet J; Bucksch K; Buecher B; Buettner R; Burn J; Caldés T; Capella G; Caron O; Casey G; Chew MH; Choi YH; Church J; Clendenning M; Colas C; Cops EJ; Coupier I; Cruz-Correa M; de la Chapelle A; de Wind N; Dębniak T; Della Valle A; Delnatte C; Dhooge M; Dominguez-Valentin M; Drouet Y; Duijkers FA; Engel C; Esperon P; Evans DG; Falcón de Vargas A; Figueiredo JC; Foulkes W; Fourme E; Frebourg T; Gallinger S; Garre P; Genuardi M; Gerdes AM; Gima LM; Giraud S; Goodwin A; Görgens H; Green K; Guillem J; Guillén-Ponce C; Guimbaud R; Guindalini RSC; Half EE; Hall MJ; Hampel H; Hansen TVO; Heinimann K; Hes FJ; Hill J; Ho JWC; Holinski-Feder E; Hoogerbrugge N; Hüneburg R; Huntley V; James PA; Jensen UB; John T; Juhari WKW; Kalady M; Kastrinos F; Kloor M; Kohonen-Corish MR; Krogh LN; Kupfer SS; Ladabaum U; Lagerstedt-Robinson K; Lalloo F, 2021, 'Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study', Lancet Oncology, 22, pp. 1014 - 1022, http://dx.doi.org/10.1016/S1470-2045(21)00189-3

Butler J; Finley C; Norell CH; Harrison S; Bryant H; Achiam MP; Altman AD; Baxter N; Bentley J; Cohen PA; Chaudry MA; Dixon E; Farrell R; Fegan S; Hashmi S; Hogdall C; Jenkins JT; Kwon J; Mala T; McNally O; Merrett N; Nelson G; Nordin A; Park J; Porter G; Reynolds J; Schieman C; Schnack T; Spigelman A; Svendsen LB; Sykes P; Thomas R, 2020, 'New approaches to cancer care in a COVID-19 world', Lancet Oncology, 21, pp. e339 - e340, http://dx.doi.org/10.1016/S1470-2045(20)30340-5

Goh LH; Spigelman AD, 2020, 'Assessing the adherence to guidelines in Lynch syndrome patients: a pilot study', ANZ Journal of Surgery, 90, pp. 1130 - 1135, http://dx.doi.org/10.1111/ans.15690

Duffy AM; Halaki M; Spigelman A; Chin V; Gallagher RM; Flood VM, 2020, 'Nutritional parameters associated with hospital admissions in patients being treated for head and neck cancer', Supportive Care in Cancer, 28, pp. 341 - 349, http://dx.doi.org/10.1007/s00520-019-04826-w

Martin I; Hawkins J; Hyer W; Attard T; Cohen S; Spigelman A; Clark SK; Latchford A, 2020, 'Upper GI in patients with FAP—the need for formal research', Gastrointestinal Endoscopy, 91, pp. 206 - 207, http://dx.doi.org/10.1016/j.gie.2019.07.031

Li A; Geyer FC; Blecua P; Lee JY; Selenica P; Brown DN; Pareja F; Lee SSK; Kumar R; Rivera B; Bi R; Piscuoglio S; Wen HY; Lozada JR; Gularte-Mérida R; Cavallone L; Aghmesheh M; Amor D; Andrews L; Antill Y; Balleine R; Beesley J; Blackburn A; Bogwitz M; Brown M; Burgess M; Burke J; Butow P; Caldon L; Campbell I; Christian A; Clarke C; Cohen P; Crook A; Cui J; Cummings M; Dawson SJ; De Fazio A; Delatycki M; Dobrovic A; Dudding T; Duijf P; Edkins E; Edwards S; Farshid G; Fellows A; Field M; Flanagan J; Fong P; Forbes J; Forrest L; Fox S; French J; Friedlander M; Ortega DG; Gattas M; Giles G; Gill G; Gleeson M; Greening S; Haan E; Harris M; Hayward N; Hickie I; Hopper J; Hunt C; James P; Jenkins M; Kefford R; Kentwell M; Kirk J; Kollias J; Lakhani S; Lindeman G; Lipton L; Lobb L; Lok S; Macrea F; Mann G; Marsh D; McLachlan SA; Meiser B; Milne R; Nightingale S; O’Connell S; Pachter N; Patterson B; Phillips K; Saleh M; Salisbury E; Saunders C; Saunus J; Scott C; Scott R; Sexton A; Shelling A; Simpson P; Spigelman A; Spurdle M; Stone J, 2019, 'Homologous recombination DNA repair defects in PALB2-associated breast cancers', Npj Breast Cancer, 5, http://dx.doi.org/10.1038/s41523-019-0115-9

Page EC; Bancroft EK; Brook MN; Assel M; Hassan Al Battat M; Thomas S; Taylor N; Chamberlain A; Pope J; Raghallaigh HN; Evans DG; Rothwell J; Maehle L; Grindedal EM; James P; Mascarenhas L; McKinley J; Side L; Thomas T; van Asperen C; Vasen H; Kiemeney LA; Ringelberg J; Jensen TD; Osther PJS; Helfand BT; Genova E; Oldenburg RA; Cybulski C; Wokolorczyk D; Ong KR; Huber C; Lam J; Taylor L; Salinas M; Feliubadaló L; Oosterwijk JC; van Zelst-Stams W; Cook J; Rosario DJ; Domchek S; Powers J; Buys S; O'Toole K; Ausems MGEM; Schmutzler RK; Rhiem K; Izatt L; Tripathi V; Teixeira MR; Cardoso M; Foulkes WD; Aprikian A; van Randeraad H; Davidson R; Longmuir M; Ruijs MWG; Helderman van den Enden ATJM; Adank M; Williams R; Andrews L; Murphy DG; Halliday D; Walker L; Liljegren A; Carlsson S; Azzabi A; Jobson I; Morton C; Shackleton K; Snape K; Hanson H; Harris M; Tischkowitz M; Taylor A; Kirk J; Susman R; Chen-Shtoyerman R; Spigelman A; Pachter N; Ahmed M; Ramon y Cajal T; Zgajnar J; Brewer C; Gadea N; Brady AF; van Os T; Gallagher D; Johannsson O; Donaldson A; Barwell J; Nicolai N; Friedman E; Obeid E; Greenhalgh L; Murthy V; Copakova L; Saya S; McGrath J; Cooke P, 2019, 'Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers', European Urology, 76, pp. 831 - 842, http://dx.doi.org/10.1016/j.eururo.2019.08.019

Li A; Geyer FC; Blecua P; Lee JY; Selenica P; Brown DN; Pareja F; Lee SSK; Kumar R; Rivera B; Bi R; Piscuoglio S; Wen HY; Lozada JR; Gularte-Mérida R; Cavallone L; Aghmesheh M; Amor D; Andrews L; Antill Y; Balleine R; Beesley J; Blackburn A; Bogwitz M; Brown M; Burgess M; Burke J; Butow P; Caldon L; Campbell I; Christian A; Clarke C; Cohen P; Crook A; Cui J; Cummings M; Dawson SJ; De Fazio A; Delatycki M; Dobrovic A; Dudding T; Duijf P; Edkins E; Edwards S; Farshid G; Fellows A; Field M; Flanagan J; Fong P; Forbes J; Forrest L; Fox S; French J; Friedlander M; Ortega DG; Gattas M; Giles G; Gill G; Gleeson M; Greening S; Haan E; Harris M; Hayward N; Hickie I; Hopper J; Hunt C; James P; Jenkins M; Kefford R; Kentwell M; Kirk J; Kollias J; Lakhani S; Lindeman G; Lipton L; Lobb L; Lok S; Macrea F; Mann G; Marsh D; McLachlan SA; Meiser B; Milne R; Nightingale S; O’Connell S; Pachter N; Patterson B; Phillips K; Saleh M; Salisbury E; Saunders C; Saunus J; Scott C; Scott R; Sexton A; Shelling A; Simpson P; Spigelman A; Spurdle M; Stone J, 2019, 'Publisher Correction: Homologous recombination DNA repair defects in PALB2-associated breast cancers (npj Breast Cancer, (2019), 5, 1, (23), 10.1038/s41523-019-0115-9)', Npj Breast Cancer, 5, http://dx.doi.org/10.1038/s41523-019-0140-8

Figlioli G; Bogliolo M; Catucci I; Caleca L; Lasheras SV; Pujol R; Kiiski JI; Muranen TA; Barnes DR; Dennis J; Michailidou K; Bolla MK; Leslie G; Aalfs CM; Balleine R; Baxter R; Braye S; Carpenter J; Dahlstrom J; Forbes J; Lee CS; Marsh D; Morey A; Pathmanathan N; Scott R; Simpson P; Spigelman A; Wilcken N; Yip D; Zeps N; Adank MA; Adlard J; Agata S; Cadoo K; Agnarsson BA; Ahearn T; Aittomäki K; Ambrosone CB; Andrews L; Anton-Culver H; Antonenkova NN; Arndt V; Arnold N; Aronson KJ; Arun BK; Asseryanis E; Auber B; Auvinen P; Azzollini J; Balmaña J; Barkardottir RB; Barrowdale D; Barwell J; Beane Freeman LE; Beauparlant CJ; Beckmann MW; Behrens S; Benitez J; Berger R; Bermisheva M; Blanco AM; Blomqvist C; Bogdanova NV; Bojesen A; Bojesen SE; Bonanni B; Borg A; Brady AF; Brauch H; Brenner H; Brüning T; Burwinkel B; Buys SS; Caldés T; Caliebe A; Caligo MA; Campa D; Campbell IG; Canzian F; Castelao JE; Chang-Claude J; Chanock SJ; Claes KBM; Clarke CL; Collavoli A; Conner TA; Cox DG; Cybulski C; Czene K; Daly MB; de la Hoya M; Devilee P; Diez O; Ding YC; Dite GS; Ditsch N; Domchek SM; Dorfling CM; dos-Santos-Silva I; Durda K, 2019, 'The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer', Npj Breast Cancer, 5, http://dx.doi.org/10.1038/s41523-019-0127-5

Dwarte T; McKay S; Johns A; Tucker K; Spigelman AD; Williams D; Stoita A, 2019, 'Genetic counselling and personalised risk assessment in the Australian pancreatic cancer screening program', Hereditary Cancer in Clinical Practice, 17, http://dx.doi.org/10.1186/s13053-019-0129-1

Rendalls S; Spigelman AD; Goodwin C; Daniel N, 2019, 'Health service engagement with consumers and community in Australia for issue: Engagement and accountability with your community', International Journal of Health Governance, 24, pp. 274 - 283, http://dx.doi.org/10.1108/IJHG-05-2019-0039

Crumbaker M; Wong J; Joshua AM; Spigelman AD, 2019, 'Outcomes of universal germline testing for men with prostate cancer in an Australian tertiary center', Asia Pacific Journal of Clinical Oncology, 15, pp. 257 - 261, http://dx.doi.org/10.1111/ajco.13148

Groves A; Gleeson M; Spigelman AD, 2019, 'NTHL1-associate polyposis: first Australian case report', Familial Cancer, 18, pp. 179 - 182, http://dx.doi.org/10.1007/s10689-018-0107-1

Bancroft EK; Saya S; Page EC; Myhill K; Thomas S; Pope J; Chamberlain A; Hart R; Glover W; Cook J; Rosario DJ; Helfand BT; Selkirk CH; Davidson R; Longmuir M; Eccles DM; Gadea N; Brewer C; Barwell J; Salinas M; Greenhalgh L; Tischkowitz M; Henderson A; Evans DG; Buys SS; Eeles RA; Aaronson NK; Eeles R; Bancroft E; Page E; Kote-Jarai Z; Ardern-Jones A; Bangma C; Castro E; Dearnaley D; Falconer A; Foster C; Gronberg H; Hamdy FC; Johannsson OT; Khoo V; Eccles D; Lilja H; Evans G; Eyfjord J; Lubinski J; Maehle L; Mikropoulos C; Millner A; Mitra A; Offman J; Moynihan C; Rennert G; Suri M; Dias A; Taylor N; D'Mello L; Pope J; James P; Mitchell G; Shanley S; Richardson K; McKinley J; Petelin L; Murphy M; Mascarenhas L; Murphy D; Lam J; Taylor L; Miller C; Stapleton A; Chong M; Suthers G; Poplawski N; Tucker K; Andrews L; Duffy J; Millard R; Ward R; Williams R; Stricker P; Kirk J; Bowman M; Patel M; Harris M; O'Connell S; Hunt C; Smyth C; Frydenberg M; Lindeman G; Shackleton K; Morton C; Susman R; McGaughran J; Boon M; Pachter N; Townshend S; Schofield L; Nicholls C; Spigelman A; Gleeson M; Amor D; Burke J; Patterson B; Swindle P; Scott R; Foulkes W; Boshari T; Aprikian A; Jensen T; Bojeson A; Osther P; Skytte A-B; Cruger D; Tondering MK; Gerdes A-M; Schmutzler R; Rhiem K; Wihler P; Kast K; Griebsch C; Johannsson O; Stefansdottir V; Murthy V; Sarin R; Awatagiri K; Ghonge S; Kowtal P; Mulgund G; Gallagher D; Bambury R; Farrell M; Gallagher F; Kiernan I; Friedman E; Chen-Shtoyerman R; Basevitch A; Leibovici D; Melzer E; Ben-Yehoshua SJ; Nicolai N; Radice P; Valdagni R; Magnani T; Gay S; Teo SH; Tan HM; Yoon S-Y; Thong MK; Vasen H; Ringleberg J; van Asperen C; Kiemeney B; van Zelst-Stams W; Ausems MGEM; van der Luijt RB; van Os T; Ruijs MWG; Adank MA; Oldenburg RA; Helderman-van den Enden APTJM; Caanen BAH; Oosterwijk JC; Moller P; Brennhovd B; Medvik H; Hanslien E; Grindedal EM; Cybulski C; Wokolorczyk D; Teixeira M; Maia S; Peixoto A; Henrique R; Oliveira J; Goncalves N; Araujo L; Seixas M; Souto JP; Nogueira P; Copakova L; Zgajnar J; Krajc M; Vrecar A; Capella G; Ramon y Cajal T; Fisas D; Mora J; Esquena S; Balmana J; Morote J; Liljegren A; Hjalm-Eriksson M; Ekdahl K-J; Carlsson S; George A; Kemp Z; Wiggins J; Moss C; Van As N; Thompson A; Ogden C; Woodhouse C; Kumar P; Evans DG; Bulman B; Rothwell J; Tricker K; Wise G; Mercer C; McBride D; Costello P; Pearce A; Torokwa A; Paterson J; Clowes V; Taylor A; Newcombe B; Walker L; Halliday D; Stayner B; Fleming-Brown D; Snape K; Hanson H; Hodgson S; Brice G; Homfray T; Hammond C; Kohut K; Anjum U; Dearing A; Mencias M; Potter A; Renton C; Searle A; Hill K; Goodman S; Garcia L; Devlin G; Everest S; Nadolski M; Douglas F; Jobson I; Paez E; Donaldson A; Tomkins S; Langman C; Jacobs C; Pichert G; Shaw A; Kulkarni A; Tripathi V; Rose S; Compton C; Watson M; Reinholtz C; Brady A; Dorkins H; Melville A; Kosicka-Slawinska M; Cummings C; Kiesel V; Bartlett M; Randhawa K; Ellery N; Side L; Male A; Simon K; Rees K; Tidey L; Gurasashvili J; Nevitt L; Ingram S; Howell A; Rosario D; Catto J; Howson J; Ong K-R; Chapman C; Cole T; Heaton T; Hoffman J; Burgess L; Huber C; Islam F; Watt C; Duncan A; Kockelbergh R; Mzazi S; Dineen A; Sattar A; Kaemba B; Sidat Z; Patel N; Siguake K; Birt A; Poultney U; Umez-Eronini N; Mom J; Sutton V; Cornford P; Bermingham N; Yesildag P; Treherne K; Griffiths J; Cogley L; Gott H; Rubinstein WS; Hulick P; McGuire M; Shevrin D; Kaul K; Weissman S; Newlin A; Vogel K; Weiss S; Hook N; Buys S; Goldgar D; Conner T; Venne V; Stephenson R; Dechet C; Domchek S; Powers J; Rustgi N; Strom S; Arun B; Davis JW; Yamamura Y; Obeid E; Giri V; Gross L; Bealin L; Cooney K; Stoffel E; Okoth L, 2019, 'Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations', BJU INTERNATIONAL, 123, pp. 284 - 292, http://dx.doi.org/10.1111/bju.14412

Butel-Simoes GI; Spigelman AD; Scott RJ; Vilain RE, 2019, 'Low-level parental mosaicism in an apparent de novo case of Peutz–Jeghers syndrome', Familial Cancer, 18, pp. 109 - 112, http://dx.doi.org/10.1007/s10689-018-0093-3

Mavaddat N; Michailidou K; Dennis J; Lush M; Fachal L; Lee A; Tyrer JP; Chen TH; Wang Q; Bolla MK; Yang X; Adank MA; Ahearn T; Aittomäki K; Allen J; Andrulis IL; Anton-Culver H; Antonenkova NN; Arndt V; Aronson KJ; Auer PL; Auvinen P; Barrdahl M; Beane Freeman LE; Beckmann MW; Behrens S; Benitez J; Bermisheva M; Bernstein L; Blomqvist C; Bogdanova NV; Bojesen SE; Bonanni B; Børresen-Dale AL; Brauch H; Bremer M; Brenner H; Brentnall A; Brock IW; Brooks-Wilson A; Brucker SY; Brüning T; Burwinkel B; Campa D; Carter BD; Castelao JE; Chanock SJ; Chlebowski R; Christiansen H; Clarke CL; Collée JM; Cordina-Duverger E; Cornelissen S; Couch FJ; Cox A; Cross SS; Czene K; Daly MB; Devilee P; Dörk T; dos-Santos-Silva I; Dumont M; Durcan L; Dwek M; Eccles DM; Ekici AB; Eliassen AH; Ellberg C; Engel C; Eriksson M; Evans DG; Fasching PA; Figueroa J; Fletcher O; Flyger H; Försti A; Fritschi L; Gabrielson M; Gago-Dominguez M; Gapstur SM; García-Sáenz JA; Gaudet MM; Georgoulias V; Giles GG; Gilyazova IR; Glendon G; Goldberg MS; Goldgar DE; González-Neira A; Grenaker Alnæs GI; Grip M; Gronwald J; Grundy A; Guénel P; Haeberle L; Hahnen E; Haiman CA; Håkansson N; Hamann U; Hankinson SE, 2019, 'Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes', American Journal of Human Genetics, 104, pp. 21 - 34, http://dx.doi.org/10.1016/j.ajhg.2018.11.002

Spigelman A; Lu M, 2019, 'Adherence to referral guidelines: Genetic testing in an Australian triple negative breast cancer (TNBC) cohort', International Journal of Health Governance,, 24, pp. 6 - 18, http://dx.doi.org/10.1108/IJHG-09-2018-0045

Joo JE; Dowty JG; Milne RL; Wong EM; Dugué PA; English D; Hopper JL; Goldgar DE; Giles GG; Southey MC; Sexton A; Christian A; Trainer A; Spigelman A; Fellows A; Shelling A; De Fazio A; Blackburn A; Crook A; Meiser B; Patterson B; Clarke C; Saunders C; Hunt C; Scott C; Amor D; Marsh D; Edkins E; Salisbury E; Haan E; Neidermayr E; Macrae F; Farshid G; Lindeman G; Chenevix-Trench G; Mann G; Gill G; Thorne H; Campbell I; Hickie I; Winship I; Goldblatt J; Flanagan J; Kollias J; Visvader J; Stone J; Taylor J; Burke J; Saunus J; Forbes J; Beesley J; Kirk J; French J; Tucker K; Wu K; Phillips K; Lipton L; Andrews L; Lobb E; Walker L; Kentwell M; Spurdle A; Cummings M; Gleeson M; Harris M; Jenkins M; Young MA; Delatycki M; Wallis M; Burgess M; Price M; Brown M; Bogwitz M; Field M; Friedlander M; Gattas M; Saleh M; Hayward N; Pachter N; Cohen P; Duijf P; James P; Simpson P; Fong P; Butow P; Williams R; Kefford R; Scott R; Balleine R; Dawson SJ; Lok S; O'Connell S; Greening S; Nightingale S; Edwards S; Fox S; McLachlan SA; Lakhani S; Thomas S; Antill Y, 2018, 'Heritable DNA methylation marks associated with susceptibility to breast cancer /631/67/69 /631/337/176/1988 /692/699/67/1347 /692/308/2056 /45 /45/61 article', Nature Communications, 9, http://dx.doi.org/10.1038/s41467-018-03058-6

Kable AK; Spigelman AD, 2018, 'Why clinicians involved with adverse events need much better support', International Journal of Health Governance, 23, pp. 312 - 315, http://dx.doi.org/10.1108/IJHG-09-2018-0049

Rankin NM; Lai M; Miller D; Beale P; Spigelman A; Prest G; Turley K; Simes J, 2018, 'Cancer multidisciplinary team meetings in practice: Results from a multi-institutional quantitative survey and implications for policy change', Asia Pacific Journal of Clinical Oncology, 14, pp. 74 - 83, http://dx.doi.org/10.1111/ajco.12765

Mikropoulos C; Selkirk CGH; Saya S; Bancroft E; Vertosick E; Dadaev T; Brendler C; Page E; Dias A; Evans DG; Rothwell J; Maehle L; Axcrona K; Richardson K; Eccles D; Jensen T; Osther PJ; Van Asperen CJ; Vasen H; Kiemeney LA; Ringelberg J; Cybulski C; Wokolorczyk D; Hart R; Glover W; Lam J; Taylor L; Salinas M; Feliubadaló L; Oldenburg R; Cremers R; Verhaegh G; Van Zelst-Stams WA; Oosterwijk JC; Cook J; Rosario DJ; Buys SS; Conner T; Domchek S; Powers J; Ausems MG; Teixeira MR; Maia S; Izatt L; Schmutzler R; Rhiem K; Foulkes WD; Boshari T; Davidson R; Ruijs M; Helderman-Van Den Enden AT; Andrews L; Walker L; Snape K; Henderson A; Jobson I; Lindeman GJ; Liljegren A; Harris M; Adank MA; Kirk J; Taylor A; Susman R; Chen-Shtoyerman R; Pachter N; Spigelman A; Side L; Zgajnar J; Mora J; Brewer C; Gadea N; Brady AF; Gallagher D; Van Os T; Donaldson A; Stefansdottir V; Barwell J; James PA; Murphy D; Friedman E; Nicolai N; Greenhalgh L; Obeid E; Murthy V; Copakova L; McGrath J; Teo SH; Strom S; Kast K; Leongamornlert DA; Chamberlain A; Pope J; Newlin AC; Aaronson N; Ardern-Jones A; Bangma C; Castro E; Dearnaley D; Eyfjord J; Falconer A, 2018, 'Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition', British Journal of Cancer, 118, pp. 266 - 276, http://dx.doi.org/10.1038/bjc.2017.429

Balachandran VP; Łuksza M; Zhao JN; Makarov V; Moral JA; Remark R; Herbst B; Askan G; Bhanot U; Senbabaoglu Y; Wells DK; Cary CIO; Grbovic-Huezo O; Attiyeh M; Medina B; Zhang J; Loo J; Saglimbeni J; Abu-Akeel M; Zappasodi R; Riaz N; Smoragiewicz M; Larkin Kelley Z; Basturk O; Gönen M; Levine AJ; Allen PJ; Fearon DT; Merad M; Gnjatic S; Iacobuzio-Donahue CA; Wolchok JD; Dematteo RP; Chan TA; Greenbaum BD; Merghoub T; Leach SD; Johns AL; Scott Mead R; Gill AJ; Chang DK; McKay SH; Chantrill LA; Chin VT; Chou A; Humphris JL; Pajic M; Steinmann A; Arshi M; Drury A; Froio D; Morgan A; Timpson P; Hermann D; Vennin C; Warren S; Pinese M; Wu J; Pinho AV; Tucker K; Andrews L; Samra JS; Arena J; Pavlakis N; High HA; Mittal A; Biankin AV; Bailey P; Martin S; Musgrove EA; Jones MD; Nourse C; Jamieson NB; Stoita A; Williams D; Spigelman A; Waddell N; Pearson JV; Patch AM; Nones K; Newell F; Mukhopadhyay P; Addala V; Kazakoff S; Holmes O; Leonard C; Wood S; Xu C; Grimmond SM; Hofmann O; Wilson PJ; Christ A; Bruxner T; Asghari R; Merrett ND; Pavey D; Das A; Goodwin A; Cosman PH; Ismail K, 2017, 'Identification of unique neoantigen qualities in long-term survivors of pancreatic cancer', Nature, 551, pp. S12 - S16, http://dx.doi.org/10.1038/nature24462

Fazekas-Lavu M; Parker A; Spigelman AD; Scott RJ; Epstein RJ; Jensen M; Samaras K, 2017, 'Thyroid cancer in a patient with lynch syndrome – case report and literature review', Therapeutics and Clinical Risk Management, 13, pp. 915 - 918, http://dx.doi.org/10.2147/TCRM.S121812

Rankin N; Lai M; Miller D; Beale P; Spigelman AD; Prest G; Turley K; Simes J, 2017, 'Evidence into practice in cancer multidisciplinary teams. Results from a multi-institutional quantitative survey and implications for policy change.', Asia-Pacific Journal of Clinical Oncology, 110, pp. 1937 - 1944, http://dx.doi.org/10.1111/ajco.1275

Spigelman AD; Rendalls S; McLaws ML; Gray A, 2016, 'Antimicrobial stewardship: Australia', International Journal of Health Governance, 21, pp. 139 - 149, http://dx.doi.org/10.1108/IJHG-02-2016-0010

Talseth-Palmer BA; Bauer DC; Sjursen W; Evans TJ; Mcphillips M; Proietto A; Otton G; Spigelman AD; Scott RJ, 2016, 'Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families', Cancer Medicine, 5, pp. 929 - 941, http://dx.doi.org/10.1002/cam4.628

Wong-Brown M; McPhillips M; Gleeson M; Spigelman AD; Meldrum CJ; Dooley S; Scott RJ, 2016, 'When is a mutation not a mutation: The case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans', Hereditary Cancer in Clinical Practice, 14, http://dx.doi.org/10.1186/s13053-015-0045-y

Pokrywczynska M; Adamowicz J; Czapiewska M; Balcerczyk D; Jundzill A; Nowacki M; Petros P; Drewa T, 2016, 'Targeted therapy for stress urinary incontinence: A systematic review based on clinical trials', Expert Opinion on Biological Therapy, 16, pp. 233 - 242, http://dx.doi.org/10.1517/14712598.2016.1118459

Spigelman AD; Rendalls S, 2015, 'Clinical governance in Australia', Clinical Governance, 20, pp. 56 - 73, http://dx.doi.org/10.1108/CGIJ-03-2015-0008

Humphris JL; Johns AL; Simpson SH; Cowley MJ; Pajic M; Chang DK; Nagrial AM; Chin VT; Chantrill LA; Pinese M; Mead RS; Gill AJ; Samra JS; Kench JG; Musgrove EA; Tucker KM; Spigelman AD; Waddell N; Grimmond SM; Biankin AV, 2014, 'Clinical and pathologic features of familial pancreatic cancer', Cancer, 120, pp. 3669 - 3675, http://dx.doi.org/10.1002/cncr.28863

Purrington KS; Slettedahl S; Bolla MK; Michailidou K; Czene K; Nevanlinna H; Bojesen SE; Andrulis IL; Cox A; Hall P; Carpenter J; Yannoukakos D; A. Haiman C; Fasching PA; Mannermaa A; Winqvist R; Brenner H; Lindblom A; Chenevix-Trench G; Benitez J; Swerdlow A; Kristensen V; Guénel P; Meindl A; Darabi H; Eriksson M; Fagerholm R; Aittomaki K; Blomqvist C; Nordestgaard BG; Nielsen SF; Flyger H; Wang X; Olswold C; Olson JE; Mulligan AM; Knight JA; Tchatchou S; Reed MWR; Cross SS; Liu J; Li J; Humphreys K; Clarke C; Scott R; Balleine R; Baxter R; Braye S; Dahlstrom J; Forbes J; Lee S; Marsh D; Morey A; Pathmanathan N; Spigelman A; Wilcken N; Yip D; Landrith S; Oeser S; Rübner M; Williams E; Ryder-Mills E; Sargus K; Colleran G; Rowan A; Jones A; Andersen DU; Arnadottir MB; Bank A; Kjeldgård D; Pita H; Alonso C; Herrero D; Álvarez N; Zamora MP; Menendez P; Lacey J; Wang S; Ma H; Lu Y; Clague J; Deapen D; Pinder R; Lee E; Schumacher F; Horn-Ross P; Reynolds P; Nelson D; Ziegler H; Wolf S; Hermann V; Hellebrand H; Engert S; Fostira F; Fountzilas G; Konstantopoulou I; Henderson BE; Le Marchand L; Ekici AB; Hartmann A, 2014, 'Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade', Human Molecular Genetics, 23, pp. 6034 - 6046, http://dx.doi.org/10.1093/hmg/ddu300

Butel-Simoes GI; Spigelman AD, 2014, 'Analysis of patient reports on the referral process to two NSW cancer genetic services', Familial Cancer, 13, pp. 333 - 343, http://dx.doi.org/10.1007/s10689-014-9710-y

Mattick JS; Dziadek MA; Terrill BN; Kaplan W; Spigelman AD; Bowling FG; Dinger ME, 2014, 'The impact of genomics on the future of medicine and health', Medical Journal of Australia, 201, pp. 17 - 20, http://dx.doi.org/10.5694/mja13.10920

Nieuwenhuis MH; Kets CM; Murphy-Ryan M; Yntema HG; Evans DG; Colas C; Møller P; Hes FJ; Hodgson SV; Olderode-Berends MJW; Aretz S; Heinimann K; Gómez García EB; Douglas F; Spigelman A; Timshel S; Lindor NM; Vasen HFA, 2014, 'Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome', Familial Cancer, 13, pp. 57 - 63, http://dx.doi.org/10.1007/s10689-013-9674-3

Teng I; Spigelman A, 2014, 'Attitudes and knowledge of medical practitioners to hereditary cancer clinics and cancer genetic testing', Familial Cancer, 13, pp. 311 - 324, http://dx.doi.org/10.1007/s10689-013-9695-y

Bancroft EK; Page EC; Castro E; Lilja H; Vickers A; Sjoberg D; Assel M; Foster CS; Mitchell G; Drew K; Mæhle L; Axcrona K; Evans DG; Bulman B; Eccles D; McBride D; Van Asperen C; Vasen H; Kiemeney LA; Ringelberg J; Cybulski C; Wokolorczyk D; Selkirk C; Hulick PJ; Bojesen A; Skytte AB; Lam J; Taylor L; Oldenburg R; Cremers R; Verhaegh G; Van Zelst-Stams WA; Oosterwijk JC; Blanco I; Salinas M; Cook J; Rosario DJ; Buys S; Conner T; Ausems MG; Ong KR; Hoffman J; Domchek S; Powers J; Teixeira MR; Maia S; Foulkes WD; Taherian N; Ruijs M; Den Enden ATHV; Izatt L; Davidson R; Adank MA; Walker L; Schmutzler R; Tucker K; Kirk J; Hodgson S; Harris M; Douglas F; Lindeman GJ; Zgajnar J; Tischkowitz M; Clowes VE; Susman R; Ramón Y Cajal T; Patcher N; Gadea N; Spigelman A; Van Os T; Liljegren A; Side L; Brewer C; Brady AF; Donaldson A; Stefansdottir V; Friedman E; Chen-Shtoyerman R; Amor DJ; Copakova L; Barwell J; Giri VN; Murthy V; Nicolai N; Teo SH; Greenhalgh L; Strom S; Henderson A; McGrath J; Gallagher D; Aaronson N; Ardern-Jones A; Bangma C; Dearnaley D; Costello P; Eyfjord J; Rothwell J; Falconer A; Gronberg H; Hamdy FC, 2014, 'Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: Results from the initial screening round of the IMPACT study', European Urology, 66, pp. 489 - 499, http://dx.doi.org/10.1016/j.eururo.2014.01.003

Talseth-Palmer BA; Wijnen JT; Andreassen EK; Barker D; Jagmohan-Changur S; Tops CM; Meldrum C; Spigelman A; Hes FJ; Van Wezel T; Vasen HFA; Scott RJ, 2013, 'The importance of a large sample cohort for studies on modifier genes influencing disease severity in FAP patients', Hereditary Cancer in Clinical Practice, 11, http://dx.doi.org/10.1186/1897-4287-11-20

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