Lea Jessop

Lea Jessop

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Lea Jessop

Lea Jessop

Publications by authors named "Lea Jessop"

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17Publications

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Detectible mosaic truncating PPM1D mutations, age and breast cancer risk.

J Hum Genet 2019 Jun 8;64(6):545-550. Epub 2019 Mar 8.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/s10038-019-0589-1DOI Listing
June 2019

Characterization of breakpoint regions of large structural autosomal mosaic events.

Hum Mol Genet 2017 11;26(22):4388-4394

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.

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http://dx.doi.org/10.1093/hmg/ddx324DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251648PMC
November 2017

Landscape of Combination Immunotherapy and Targeted Therapy to Improve Cancer Management.

Cancer Res 2017 07 26;77(13):3666-3671. Epub 2017 Apr 26.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1158/0008-5472.CAN-16-3338DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522610PMC
July 2017

Burden of Nonsynonymous Mutations among TCGA Cancers and Candidate Immune Checkpoint Inhibitor Responses.

Cancer Res 2016 07 18;76(13):3767-72. Epub 2016 May 18.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1158/0008-5472.CAN-16-0170DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4930685PMC
July 2016

Functional characterization of the 12p12.1 renal cancer-susceptibility locus implicates BHLHE41.

Nat Commun 2016 07 7;7:12098. Epub 2016 Jul 7.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, 8717 Grovemont Circle, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/ncomms12098DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941055PMC
July 2016

Characterization of large structural genetic mosaicism in human autosomes.

Authors:
Mitchell J Machiela Weiyin Zhou Joshua N Sampson Michael C Dean Kevin B Jacobs Amanda Black Louise A Brinton I-Shou Chang Chu Chen Constance Chen Kexin Chen Linda S Cook Marta Crous Bou Immaculata De Vivo Jennifer Doherty Christine M Friedenreich Mia M Gaudet Christopher A Haiman Susan E Hankinson Patricia Hartge Brian E Henderson Yun-Chul Hong H Dean Hosgood Chao A Hsiung Wei Hu David J Hunter Lea Jessop Hee Nam Kim Yeul Hong Kim Young Tae Kim Robert Klein Peter Kraft Qing Lan Dongxin Lin Jianjun Liu Loic Le Marchand Xiaolin Liang Jolanta Lissowska Lingeng Lu Anthony M Magliocco Keitaro Matsuo Sara H Olson Irene Orlow Jae Yong Park Loreall Pooler Jennifer Prescott Radhai Rastogi Harvey A Risch Fredrick Schumacher Adeline Seow Veronica Wendy Setiawan Hongbing Shen Xin Sheng Min-Ho Shin Xiao-Ou Shu David VanDen Berg Jiu-Cun Wang Nicolas Wentzensen Maria Pik Wong Chen Wu Tangchun Wu Yi-Long Wu Lucy Xia Hannah P Yang Pan-Chyr Yang Wei Zheng Baosen Zhou Christian C Abnet Demetrius Albanes Melinda C Aldrich Christopher Amos Laufey T Amundadottir Sonja I Berndt William J Blot Cathryn H Bock Paige M Bracci Laurie Burdett Julie E Buring Mary A Butler Tania Carreón Nilanjan Chatterjee Charles C Chung Michael B Cook Michael Cullen Faith G Davis Ti Ding Eric J Duell Caroline G Epstein Jin-Hu Fan Jonine D Figueroa Joseph F Fraumeni Neal D Freedman Charles S Fuchs Yu-Tang Gao Susan M Gapstur Ana Patiño-Garcia Montserrat Garcia-Closas J Michael Gaziano Graham G Giles Elizabeth M Gillanders Edward L Giovannucci Lynn Goldin Alisa M Goldstein Mark H Greene Goran Hallmans Curtis C Harris Roger Henriksson Elizabeth A Holly Robert N Hoover Nan Hu Amy Hutchinson Mazda Jenab Christoffer Johansen Kay-Tee Khaw Woon-Puay Koh Laurence N Kolonel Charles Kooperberg Vittorio Krogh Robert C Kurtz Andrea LaCroix Annelie Landgren Maria Teresa Landi Donghui Li Linda M Liao Nuria Malats Katherine A McGlynn Lorna H McNeill Robert R McWilliams Beatrice S Melin Lisa Mirabello Beata Peplonska Ulrike Peters Gloria M Petersen Ludmila Prokunina-Olsson Mark Purdue You-Lin Qiao Kari G Rabe Preetha Rajaraman Francisco X Real Elio Riboli Benjamín Rodríguez-Santiago Nathaniel Rothman Avima M Ruder Sharon A Savage Ann G Schwartz Kendra L Schwartz Howard D Sesso Gianluca Severi Debra T Silverman Margaret R Spitz Victoria L Stevens Rachael Stolzenberg-Solomon Daniel Stram Ze-Zhong Tang Philip R Taylor Lauren R Teras Geoffrey S Tobias Kala Viswanathan Sholom Wacholder Zhaoming Wang Stephanie J Weinstein William Wheeler Emily White John K Wiencke Brian M Wolpin Xifeng Wu Jay S Wunder Kai Yu Krista A Zanetti Anne Zeleniuch-Jacquotte Regina G Ziegler Mariza de Andrade Kathleen C Barnes Terri H Beaty Laura J Bierut Karl C Desch Kimberly F Doheny Bjarke Feenstra David Ginsburg John A Heit Jae H Kang Cecilia A Laurie Jun Z Li William L Lowe Mary L Marazita Mads Melbye Daniel B Mirel Jeffrey C Murray Sarah C Nelson Louis R Pasquale Kenneth Rice Janey L Wiggs Anastasia Wise Margaret Tucker Luis A Pérez-Jurado Cathy C Laurie Neil E Caporaso Meredith Yeager Stephen J Chanock

Am J Hum Genet 2015 Mar;96(3):487-97

Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Bethesda, MD 20892, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.01.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375431PMC
March 2015

RAD51B Activity and Cell Cycle Regulation in Response to DNA Damage in Breast Cancer Cell Lines.

Breast Cancer (Auckl) 2014 12;8:135-44. Epub 2014 Oct 12.

Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.4137/BCBCR.S17766DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4213955PMC
November 2014

BLM helicase ortholog Sgs1 is a central regulator of meiotic recombination intermediate metabolism.

Mol Cell 2012 Apr;46(1):43-53

Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1016/j.molcel.2012.02.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3328772PMC
April 2012

Sequence analysis of the shelterin telomere protection complex genes in dyskeratosis congenita.

J Med Genet 2011 Apr 5;48(4):285-8. Epub 2011 Jan 5.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, Bethesda, MD, USA.

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http://dx.doi.org/10.1136/jmg.2010.082727DOI Listing
April 2011

Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenita.

Genes Dev 2011 Jan;25(1):11-6

Department of Medicine, Stanford University School of Medicine, Stanford, California 94305, USA.

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http://dx.doi.org/10.1101/gad.2006411DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012932PMC
January 2011

Mus81/Mms4 endonuclease and Sgs1 helicase collaborate to ensure proper recombination intermediate metabolism during meiosis.

Mol Cell 2008 Aug;31(3):313-23

Laboratory of Biochemistry and Molecular Biology, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892-4260, USA.

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http://dx.doi.org/10.1016/j.molcel.2008.05.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584117PMC
August 2008

Meiotic chromosome synapsis-promoting proteins antagonize the anti-crossover activity of sgs1.

PLoS Genet 2006 Sep 2;2(9):e155. Epub 2006 Aug 2.

Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.0020155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1570379PMC
September 2006

Infrequent co-conversion of markers flanking a meiotic recombination initiation site in Saccharomyces cerevisiae.

Genetics 2005 Mar 16;169(3):1353-67. Epub 2005 Jan 16.

Center for Cancer Research, National Cancer Institute, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1534/genetics.104.036509DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1449552PMC
March 2005