1. Activating genomic alterations in the Gs alpha gene (GNAS) in 274 694 tumors. Issue 9 (14th May 2020) Authors: Tirosh, Amit; Jin, Dexter X.; De Marco, Luiz; Laitman, Yael; Friedman, Eitan Journal: Genes, chromosomes & cancer Issue: Volume 59:Issue 9(2020) Page Start: 503 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers. Issue 1 (December 2015) Authors: Blein, Sophie; Bardel, Claire; Danjean, Vincent; McGuffog, Lesley; Healey, Sue; Barrowdale, Daniel; Lee, Andrew; Dennis, Joe; Kuchenbaecker, Karoline; Soucy, Penny; Terry, Mary; Chung, Wendy; Goldgar, David; Buys, Saundra; Janavicius, Ramunas; Tihomirova, Laima; Tung, Nadine; Dorfling, Cecilia; v... Journal: Breast cancer research Issue: Volume 17:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Breast cancer surveillance for BRCA1/2 mutation carriers – is "early detection" early enough?. (February 2020) Authors: Bernstein-Molho, Rinat; Kaufman, Bella; Ben David, Merav A.; Sklair-Levy, Miri; Feldman, Dana Madoursky; Zippel, Dov; Laitman, Yael; Friedman, Eitan Journal: Breast Issue: Volume 49(2020) Page Start: 81 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Common Susceptibility Loci for Male Breast Cancer. (12th August 2020) Authors: Maguire, Sarah; Perraki, Eleni; Tomczyk, Katarzyna; Jones, Michael E; Fletcher, Olivia; Pugh, Matthew; Winter, Timothy; Thompson, Kyle; Cooke, Rosie; Trainer, Alison; James, Paul; Bojesen, Stig; Flyger, Henrik; Nevanlinna, Heli; Mattson, Johanna; Friedman, Eitan; Laitman, Yael; Palli, Domenico; M... Journal: Journal of the National Cancer Institute Issue: Volume 113:Number 4(2021) Page Start: 453 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. De novo mutation in MEN1 is not associated with parental somatic mosaicism. Issue 1 (January 2017) Authors: Laitman, Yael; Jaffe, Anat; Schayek, Hagit; Friedman, Eitan Journal: Endocrine-related cancer Issue: Volume 24:Issue 1(2017) Page Start: L1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Germline variant in REXO2 is a novel candidate gene in familial pheochromocytoma. (2020) Authors: Laitman, Yael; Tzur, Shay; Attali, Ruben; Tirosh, Amit; Friedman, Eitan Journal: Genetical research Issue: Volume 102(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study. (12th October 2018) Authors: Qian, Frank; Wang, Shengfeng; Mitchell, Jonathan; McGuffog, Lesley; Barrowdale, Daniel; Leslie, Goska; Oosterwijk, Jan C; Chung, Wendy K; Evans, D Gareth; Engel, Christoph; Kast, Karin; Aalfs, Cora M; Adank, Muriel A; Adlard, Julian; Agnarsson, Bjarni A; Aittomäki, Kristiina; Alducci, Elisa; Andr... Journal: Journal of the National Cancer Institute Issue: Volume 111:Number 4(2019) Page Start: 350 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Issue 1 (December 2016) Authors: Zeng, Chenjie; Guo, Xingyi; Long, Jirong; Kuchenbaecker, Karoline; Droit, Arnaud; Michailidou, Kyriaki; Ghoussaini, Maya; Kar, Siddhartha; Freeman, Adam; Hopper, John; Milne, Roger; Bolla, Manjeet; Wang, Qin; Dennis, Joe; Agata, Simona; Ahmed, Shahana; Aittomäki, Kristiina; Andrulis, Irene; Anton... Journal: Breast cancer research Issue: Volume 18:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32, 295 women. Issue 1 (December 2016) Authors: Rebbeck, Timothy; Friebel, Tara; Mitra, Nandita; Wan, Fei; Chen, Stephanie; Andrulis, Irene; Apostolou, Paraskevi; Arnold, Norbert; Arun, Banu; Barrowdale, Daniel; Benitez, Javier; Berger, Raanan; Berthet, Pascaline; Borg, Ake; Buys, Saundra; Caldes, Trinidad; Carter, Jonathan; Chiquette, Jocelyn... Journal: Breast cancer research Issue: Volume 18:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. 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 View Content: Available online (eLD content is only available in our Reading Rooms) ↗