scholarly article | Q13442814 |
P50 | author | Aleksandra Gentry-Maharaj | Q30001996 |
Thilo Dörk | Q37342847 | ||
Kunle Odunsi | Q38296739 | ||
Lara Sucheston-Campbell | Q38305275 | ||
Alice S. Whittemore | Q42423380 | ||
Australian Ovarian Cancer Study Group | Q42790423 | ||
Susan J. Ramus | Q45906365 | ||
David Bowtell | Q47451431 | ||
Usha Menon | Q55130377 | ||
Kathryn Alsop | Q56840332 | ||
Paul D P Pharoah | Q61822938 | ||
Julie M. Cunningham | Q67440680 | ||
Martin Widschwendter | Q71025350 | ||
Natalia V. Bogdanova | Q74171899 | ||
Brooke L Fridley | Q86514651 | ||
Ellen L Goode | Q88243694 | ||
Kirsten Moysich | Q90007553 | ||
Peter Hillemanns | Q91084009 | ||
Simon A Gayther | Q91677076 | ||
Honglin Song | Q91866986 | ||
Beth Karlan | Q95982319 | ||
Patricia Harrington | Q96766314 | ||
Weiva Sieh | Q98780189 | ||
Valerie McGuire | Q114314375 | ||
Shashi Lele | Q114374800 | ||
Ovarian Cancer Association Consortium | Q114374820 | ||
Samantha R Poblete | Q114374831 | ||
Mine S. Cicek | Q114374866 | ||
Maria P Intermaggio | Q114374949 | ||
Jenny Lester | Q115727450 | ||
P2093 | author name string | Ed Dicks | |
Caroline Baynes | |||
P2860 | cites work | The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 |
Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer | Q28388006 | ||
Fast and accurate long-read alignment with Burrows-Wheeler transform | Q29547193 | ||
Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium | Q29619206 | ||
The time interval from surgery to start of chemotherapy significantly impacts prognosis in patients with advanced serous ovarian carcinoma - analysis of patient data in the prospective OVCAD study | Q30656720 | ||
The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population | Q33991747 | ||
A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes | Q34115258 | ||
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer | Q36956156 | ||
Prognostic impact of the time interval between surgery and chemotherapy in advanced ovarian cancer: analysis of prospective randomised phase III trials | Q43868430 | ||
PPM1D mutations in circulating white blood cells and the risk for ovarian cancer. | Q51182994 | ||
RE: PPM1D mutations in circulating white blood cells and the risk for ovarian cancer | Q57097208 | ||
Contribution ofBRCA1andBRCA2mutations to inherited ovarian cancer | Q59688934 | ||
Molecular wanderings through the DNA damage response and risk for ovarian cancer | Q86821628 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | ovarian cancer | Q172341 |
P577 | publication date | 2016-01-27 | |
P1433 | published in | Journal of the National Cancer Institute | Q400279 |
P1476 | title | PPM1D Mosaic Truncating Variants in Ovarian Cancer Cases May Be Treatment-Related Somatic Mutations | |
P478 | volume | 108 |
Q91211233 | Cancer genetics, precision prevention and a call to action |
Q34548829 | Clonal Hematopoiesis Associated With Adverse Outcomes After Autologous Stem-Cell Transplantation for Lymphoma. |
Q89651152 | Clonal hematopoiesis in cancer |
Q34556382 | Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly |
Q40063882 | De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome |
Q92237320 | Detectible mosaic truncating PPM1D mutations, age and breast cancer risk |
Q37624593 | Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel |
Q47157222 | Mosaic mutations in blood DNA sequence are associated with solid tumor cancers |
Q57284432 | Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings |
Q58547326 | PPM1D Mutations Drive Clonal Hematopoiesis in Response to Cytotoxic Chemotherapy |
Q89320681 | PPM1D-truncating mutations confer resistance to chemotherapy and sensitivity to PPM1D inhibition in hematopoietic cells |
Q40397279 | Predictors of pretreatment CA125 at ovarian cancer diagnosis: a pooled analysis in the Ovarian Cancer Association Consortium |
Q93046091 | Somatic mosaic truncating mutations of PPM1D in blood can result from expansion of a mutant clone under selective pressure of chemotherapy |
Q30239099 | The ageing genome, clonal mosaicism and chronic disease |
Q89479770 | The role of PPM1D in cancer and advances in studies of its inhibitors |
Q38627087 | Therapy-Related Clonal Hematopoiesis in Patients with Non-hematologic Cancers Is Common and Associated with Adverse Clinical Outcomes |
Q30240431 | Therapy-related myeloid neoplasms: does knowing the origin help to guide treatment? |
Q38611096 | Therapy-related myeloid neoplasms: when genetics and environment collide |
Q39613092 | Truncating and missense PPM1D mutations in early-onset and/or familial/hereditary prostate cancer patients. |
Q99572138 | Unique roles of rare variants in the genetics of complex diseases in humans |
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