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Author/Creator Eason, Jacqueline

1. Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores. (28th July 2021)

Authors:
Barnes, Daniel R; Silvestri, Valentina; Leslie, Goska; McGuffog, Lesley; Dennis, Joe; Yang, Xin; Adlard, Julian; Agnarsson, Bjarni A; Ahmed, Munaza; Aittomäki, Kristiina; Andrulis, Irene L; Arason, Adalgeir; Arnold, Norbert; Auber, Bernd; Azzollini, Jacopo; Balmaña, Judith; Barkardottir, Rosa B; ...
Journal:
Journal of the National Cancer Institute
Issue:
Volume 114:Number 1(2022)
Page Start:
109
Record Type:
Journal Article
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2. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants. Issue 14 (10th May 2022)

Authors:
Li, Shuai; Silvestri, Valentina; Leslie, Goska; Rebbeck, Timothy R.; Neuhausen, Susan L.; Hopper, John L.; Nielsen, Henriette Roed; Lee, Andrew; Yang, Xin; McGuffog, Lesley; Parsons, Michael T.; Andrulis, Irene L.; Arnold, Norbert; Belotti, Muriel; Borg, Åke; Buecher, Bruno; Buys, Saundra S.; Cap...
Journal:
Journal of clinical oncology
Issue:
Volume 40:Issue 14(2022)
Page Start:
1529
Record Type:
Journal Article
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3. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing. (3rd December 2017)

Authors:
Stals, Karen L.; Wakeling, Matthew; Baptista, Júlia; Caswell, Richard; Parrish, Andrew; Rankin, Julia; Tysoe, Carolyn; Jones, Garan; Gunning, Adam C.; Lango Allen, Hana; Bradley, Lisa; Brady, Angela F.; Carley, Helena; Carmichael, Jenny; Castle, Bruce; Cilliers, Deirdre; Cox, Helen; Deshpande, Ch...
Journal:
Prenatal diagnosis
Issue:
Volume 38:Number 1(2018)
Page Start:
33
Record Type:
Journal Article
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4. Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data. Issue 10 (29th July 2022)

Authors:
Hardcastle, Amy; Berry, Aliska M.; Campbell, Ian M.; Zhao, Xiaonan; Liu, Pengfei; Gerard, Amanda E.; Rosenfeld, Jill A.; Sisoudiya, Saumya D.; Hernandez‐Garcia, Andres; Loddo, Sara; Di Tommaso, Silvia; Novelli, Antonio; Dentici, Maria L.; Capolino, Rossella; Digilio, Maria C.; Graziani, Ludovico;...
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 10(2022)
Page Start:
2958
Record Type:
Journal Article
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5. Mutational spectrum in a worldwide study of 29, 700 families with BRCA1 or BRCA2 mutations. Issue 5 (12th March 2018)

Authors:
Rebbeck, Timothy R.; Friebel, Tara M.; Friedman, Eitan; Hamann, Ute; Huo, Dezheng; Kwong, Ava; Olah, Edith; Olopade, Olufunmilayo I.; Solano, Angela R.; Teo, Soo‐Hwang; Thomassen, Mads; Weitzel, Jeffrey N.; Chan, TL; Couch, Fergus J.; Goldgar, David E.; Kruse, Torben A.; Palmero, Edenir Inêz; Par...
Journal:
Human mutation
Issue:
Volume 39:Issue 5(2018)
Page Start:
593
Record Type:
Journal Article
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8. Risks of breast or ovarian cancer in BRCA1 or BRCA2 predictive test negatives: findings from the EMBRACE study. (December 2018)

Authors:
Girardi, Fabio; Barnes, Daniel; Barrowdale, Daniel; Frost, Debra; Brady, Angela; Miller, Claire; Henderson, Alex; Donaldson, Alan; Murray, Alex; Brewer, Carole; Pottinger, Caroline; Evans, D Gareth; Eccles, Diana; Lalloo, Fiona; Gregory, Helen; Cook, Jackie; Eason, Jacqueline; Adlard, Julian; Bar...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 12(2018)
Page Start:
1575
Record Type:
Journal Article
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