전남대학교 중앙도서관

A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome

학술저널

issue: Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-15 (2023)
Author: Romy Walker
Khalid Mahmood
Jihoon E. Joo
Mark Clendenning
Peter Georgeson
Julia Como
Sharelle Joseland
Susan G. Preston
Yoland Antill
Rachel Austin
Alex Boussioutas
Michelle Bowman
Jo Burke
Ainsley Campbell
Simin Daneshvar
Emma Edwards
Margaret Gleeson
Annabel Goodwin
Marion T. Harris
Alex Henderson
Megan Higgins
John L. Hopper
Ryan A. Hutchinson
Emilia Ip
Joanne Isbister
Kais Kasem
Helen Marfan
Di Milnes
Annabelle Ng
Cassandra Nichols
Shona O’Connell
Nicholas Pachter
Bernard J. Pope
Nicola Poplawski
Abiramy Ragunathan
Courtney Smyth
Allan Spigelman
Kirsty Storey
Rachel Susman
Jessica A. Taylor
Linda Warwick
Mathilda Wilding
Rachel Williams
Aung K. Win
Michael D. Walsh
Finlay A. Macrae
Mark A. Jenkins
Christophe Rosty
Ingrid M. Winship
Daniel D. Buchanan
for the Family Cancer Clinics of Australia
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Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium

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issue: Hereditary Cancer in Clinical Practice, Vol 20, Iss 1, Pp 1-11 (2022)
Author: Pål Møller
Toni Seppälä
James G. Dowty
Saskia Haupt
Mev Dominguez-Valentin
Lone Sunde
Inge Bernstein
Christoph Engel
Stefan Aretz
Maartje Nielsen
Gabriel Capella
Dafydd Gareth Evans
John Burn
Elke Holinski-Feder
Lucio Bertario
Bernardo Bonanni
Annika Lindblom
Zohar Levi
Finlay Macrae
Ingrid Winship
John-Paul Plazzer
Rolf Sijmons
Luigi Laghi
Adriana Della Valle
Karl Heinimann
Elizabeth Half
Francisco Lopez-Koestner
Karin Alvarez-Valenzuela
Rodney J. Scott
Lior Katz
Ido Laish
Elez Vainer
Carlos Alberto Vaccaro
Dirce Maria Carraro
Nathan Gluck
Naim Abu-Freha
Aine Stakelum
Rory Kennelly
Des Winter
Benedito Mauro Rossi
Marc Greenblatt
Mabel Bohorquez
Harsh Sheth
Maria Grazia Tibiletti
Leonardo S. Lino-Silva
Karoline Horisberger
Carmen Portenkirchner
Ivana Nascimento
Norma Teresa Rossi
Leandro Apolinário da Silva
Huw Thomas
Attila Zaránd
Jukka-Pekka Mecklin
Kirsi Pylvänäinen
Laura Renkonen-Sinisalo
Anna Lepisto
Päivi Peltomäki
Christina Therkildsen
Lars Joachim Lindberg
Ole Thorlacius-Ussing
Magnus von Knebel Doeberitz
Markus Loeffler
Nils Rahner
Verena Steinke-Lange
Wolff Schmiegel
Deepak Vangala
Claudia Perne
Robert Hüneburg
Aída Falcón de Vargas
Andrew Latchford
Anne-Marie Gerdes
Ann-Sofie Backman
Carmen Guillén-Ponce
Carrie Snyder
Charlotte K. Lautrup
David Amor
Edenir Palmero
Elena Stoffel
Floor Duijkers
Michael J. Hall
Heather Hampel
Heinric Williams
Henrik Okkels
Jan Lubiński
Jeanette Reece
Joanne Ngeow
Jose G. Guillem
Julie Arnold
Karin Wadt
Kevin Monahan
Leigha Senter
Lene J. Rasmussen
Liselotte P. van Hest
Luigi Ricciardiello
Maija R. J. Kohonen-Corish
Marjolijn J. L. Ligtenberg
Melissa Southey
Melyssa Aronson
Mohd N. Zahary
N. Jewel Samadder
Nicola Poplawski
Nicoline Hoogerbrugge
Patrick J. Morrison
Paul James
Grant Lee
Rakefet Chen-Shtoyerman
Ravindran Ankathil
Rish Pai
Robyn Ward
Susan Parry
Tadeusz Dębniak
Thomas John
Thomas van Overeem Hansen
Trinidad Caldés
Tatsuro Yamaguchi
Verónica Barca-Tierno
Pilar Garre
Giulia Martina Cavestro
Jürgen Weitz
Silke Redler
Reinhard Büttner
Vincent Heuveline
John L. Hopper
Aung Ko Win
Noralane Lindor
Steven Gallinger
Loïc Le Marchand
Polly A. Newcomb
Jane Figueiredo
Daniel D. Buchanan
Stephen N. Thibodeau
Sanne W. ten Broeke
Eivind Hovig
Sigve Nakken
Marta Pineda
Nuria Dueñas
Joan Brunet
Kate Green
Fiona Lalloo
Katie Newton
Emma J. Crosbie
Miriam Mints
Douglas Tjandra
Florencia Neffa
Patricia Esperon
Revital Kariv
Guy Rosner
Walter Hernán Pavicic
Pablo Kalfayan
Giovana Tardin Torrezan
Thiago Bassaneze
Claudia Martin
Gabriela Moslein
Aysel Ahadova
Matthias Kloor
Julian R. Sampson
Mark A. Jenkins
The European Hereditary Tumour Group (EHTG) and the International Mismatch Repair Consortium (IMRC)
DB Label: Database : Directory of Open Access Journals

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Population-based estimates of breast cancer risk for carriers of pathogenic variants identified by gene-panel testing

학술저널

issue: npj Breast Cancer, Vol 7, Iss 1, Pp 1-7 (2021)
Author: Melissa C. Southey
James G. Dowty
Moeen Riaz
Jason A. Steen
Anne-Laure Renault
Katherine Tucker
Judy Kirk
Paul James
Ingrid Winship
Nicholas Pachter
Nicola Poplawski
Scott Grist
Daniel J. Park
Bernard J. Pope
Khalid Mahmood
Fleur Hammet
Maryam Mahmoodi
Helen Tsimiklis
Derrick Theys
Amanda Rewse
Amanda Willis
April Morrow
Catherine Speechly
Rebecca Harris
Robert Sebra
Eric Schadt
Paul Lacaze
John J. McNeil
Graham G. Giles
Roger L. Milne
John L. Hopper
Tú Nguyen-Dumont
DB Label: Database : Directory of Open Access Journals

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A case of Carney triad complicated by renal cell carcinoma and a germline SDHA pathogenic variant

학술저널

issue: Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-6 (2021)
Author: Rachel Wurth
Abhishek Jha
Crystal Kamilaris
Anthony J Gill
Nicola Poplawski
Paraskevi Xekouki
Martha M Quezado
Karel Pacak
Constantine A Stratakis
Fady Hannah-Shmouni
DB Label: Database : Directory of Open Access Journals

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BAP1 Tumour Predisposition Syndrome Due to Whole BAP1 Gene Deletion

학술저널

issue: Case Reports in Genetics, Vol 2022 (2022)
Author: Dinusha Pandithan
Sonja Klebe
Grace McKavanagh
Lesley Rawlings
Sui Yu
Jillian Nicholl
Nicola Poplawski
DB Label: Database : Directory of Open Access Journals

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Breast cancer in patients with germline TP53 pathogenic variants have typical tumour characteristics: the Cohort study of TP53 carrier early onset breast cancer (COPE study)

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