Suchergebnisse - "Scheet, Paul"

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    A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase von Scheet, Paul, Stephens, Matthew

    ISSN: 0002-9297
    Veröffentlicht: United States 01.04.2006
    Veröffentlicht in American journal of human genetics (01.04.2006)
    “… We present a statistical model for patterns of genetic variation in samples of unrelated individuals from natural populations. This model is based on the idea …”
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    Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation von Stephens, Matthew, Scheet, Paul

    ISSN: 0002-9297
    Veröffentlicht: United States 01.03.2005
    Veröffentlicht in American journal of human genetics (01.03.2005)
    “… Although many algorithms exist for estimating haplotypes from genotype data, none of them take full account of both the decay of linkage disequilibrium (LD) …”
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    Clonal evolution in breast cancer revealed by single nucleus genome sequencing von Wang, Yong, Waters, Jill, Leung, Marco L., Unruh, Anna, Roh, Whijae, Shi, Xiuqing, Chen, Ken, Scheet, Paul, Vattathil, Selina, Liang, Han, Multani, Asha, Zhang, Hong, Zhao, Rui, Michor, Franziska, Meric-Bernstam, Funda, Navin, Nicholas E.

    ISSN: 0028-0836, 1476-4687, 1476-4687
    Veröffentlicht: London Nature Publishing Group UK 14.08.2014
    Veröffentlicht in Nature (London) (14.08.2014)
    “… Sequencing studies of breast tumour cohorts have identified many prevalent mutations, but provide limited insight into the genomic diversity within tumours …”
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    MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes von Li, Yun, Willer, Cristen J., Ding, Jun, Scheet, Paul, Abecasis, Gonçalo R.

    ISSN: 0741-0395, 1098-2272, 1098-2272
    Veröffentlicht: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.12.2010
    Veröffentlicht in Genetic epidemiology (01.12.2010)
    “… Genome‐wide association studies (GWAS) can identify common alleles that contribute to complex disease susceptibility. Despite the large number of SNPs assessed …”
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    Somatic mutation load of estrogen receptor-positive breast tumors predicts overall survival: an analysis of genome sequence data von Haricharan, Svasti, Bainbridge, Matthew N., Scheet, Paul, Brown, Powel H.

    ISSN: 0167-6806, 1573-7217, 1573-7217
    Veröffentlicht: Boston Springer US 01.07.2014
    Veröffentlicht in Breast cancer research and treatment (01.07.2014)
    “… Breast cancer is one of the most commonly diagnosed cancers in women. While there are several effective therapies for breast cancer and important single gene …”
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    Early Events in the Molecular Pathogenesis of Lung Cancer von Kadara, Humam, Scheet, Paul, Wistuba, Ignacio I, Spira, Avrum E

    ISSN: 1940-6215, 1940-6215
    Veröffentlicht: United States 01.07.2016
    Veröffentlicht in Cancer prevention research (Philadelphia, Pa.) (01.07.2016)
    “… The majority of cancer-related deaths in the United States and worldwide are attributed to lung cancer. There are more than 90 million smokers in the United …”
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    The Transcriptomic Landscape of Mismatch Repair-Deficient Intestinal Stem Cells von Bommi, Prashant V, Bowen, Charles M, Reyes-Uribe, Laura, Wu, Wenhui, Katayama, Hiroyuki, Rocha, Pedro, Parra, Edwin R, Francisco-Cruz, Alejandro, Ozcan, Zuhal, Tosti, Elena, Willis, Jason A, Wu, Hong, Taggart, Melissa W, Burks, Jared K, Lynch, Patrick M, Edelmann, Winfried, Scheet, Paul A, Wistuba, Ignacio I, Sinha, Krishna M, Hanash, Samir M, Vilar, Eduardo

    ISSN: 1538-7445, 1538-7445
    Veröffentlicht: United States 15.05.2021
    Veröffentlicht in Cancer research (Chicago, Ill.) (15.05.2021)
    “… Lynch syndrome is the most common cause of hereditary colorectal cancer and is secondary to germline alterations in one of four DNA mismatch repair (MMR) …”
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    Defining the Comprehensive Genomic Landscapes of Pancreatic Ductal Adenocarcinoma Using Real-World Endoscopic Aspiration Samples von Semaan, Alexander, Bernard, Vincent, Lee, Jaewon J, Wong, Justin W, Huang, Jonathan, Swartzlander, Daniel B, Stephens, Bret M, Monberg, Maria E, Weston, Brian R, Bhutani, Manoop S, Chang, Kyle, Scheet, Paul A, Maitra, Anirban, Jakubek, Yasminka A, Guerrero, Paola A

    ISSN: 1557-3265, 1557-3265
    Veröffentlicht: United States 15.02.2021
    Veröffentlicht in Clinical cancer research (15.02.2021)
    “… Most patients with pancreatic ductal adenocarcinoma (PDAC) present with surgically unresectable cancer. As a result, endoscopic ultrasound-guided fine-needle …”
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    Genomic Landscape of Atypical Adenomatous Hyperplasia Reveals Divergent Modes to Lung Adenocarcinoma von Sivakumar, Smruthy, Lucas, F Anthony San, McDowell, Tina L, Lang, Wenhua, Xu, Li, Fujimoto, Junya, Zhang, Jianjun, Futreal, P Andrew, Fukuoka, Junya, Yatabe, Yasushi, Dubinett, Steven M, Spira, Avrum E, Fowler, Jerry, Hawk, Ernest T, Wistuba, Ignacio I, Scheet, Paul, Kadara, Humam

    ISSN: 1538-7445, 1538-7445
    Veröffentlicht: United States 15.11.2017
    Veröffentlicht in Cancer research (Chicago, Ill.) (15.11.2017)
    “… There is a dearth of knowledge about the pathogenesis of premalignant lung lesions, especially for atypical adenomatous hyperplasia (AAH), the only known …”
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    Attention-deficit/hyperactivity disorder polygenic risk scores predict attention problems in a population-based sample of children von Groen-Blokhuis, Maria M, Middeldorp, Christel M, Kan, Kees-Jan, Abdellaoui, Abdel, van Beijsterveldt, Catharina E M, Ehli, Erik A, Davies, Gareth E, Scheet, Paul A, Xiao, Xiangjun, Hudziak, James J, Hottenga, Jouke-Jan, Neale, Ben M, Boomsma, Dorret I

    ISSN: 1527-5418, 1527-5418
    Veröffentlicht: United States 01.10.2014
    “… Clinically, attention-deficit/hyperactivity disorder (ADHD) is characterized by hyperactivity, impulsivity, and inattention and is among the most common …”
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    Leveraging existing cohort studies of Mexican women to better understand Hispanic health and cancer risk von Stern, Dalia, Gomez-Flores-Ramos, Liliana, Trabert, Britton, Setiawan, V. Wendy, Le Marchand, Loïc, Gomez, Henry, Scheet, Paul A., Parada, Humberto, Pirzada, Amber, Lajous, Martin, Farland, Leslie V.

    ISSN: 0957-5243, 1573-7225, 1573-7225
    Veröffentlicht: Cham Springer International Publishing 01.09.2025
    Veröffentlicht in Cancer causes & control (01.09.2025)
    “… Background Hispanics have been historically underrepresented in epidemiologic cancer research. Existing cohort studies focused on recruiting Hispanic …”
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    RAD21 promotes oncogenesis and lethal progression of prostate cancer von Su, Xiaofeng A, Stopsack, Konrad H, Schmidt, Daniel R, Ma, Duanduan, Li, Zhe, Scheet, Paul A, Penney, Kathryn L, Lotan, Tamara L, Abida, Wassim, DeArment, Elise G, Lu, Kate, Janas, Thomas, Hu, Sofia, Vander Heiden, Matthew G, Loda, Massimo, Boselli, Monica, Amon, Angelika, Mucci, Lorelei A

    ISSN: 1091-6490, 1091-6490
    Veröffentlicht: United States 03.09.2024
    “… Higher levels of aneuploidy, characterized by imbalanced chromosome numbers, are associated with lethal progression in prostate cancer. However, how aneuploidy …”
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    Causes of Clonal Hematopoiesis: a Review von Joo, LiJin, Bradley, Catherine C., Lin, Steven H., Scheet, Paul A., Nead, Kevin T.

    ISSN: 1523-3790, 1534-6269, 1534-6269
    Veröffentlicht: New York Springer US 01.03.2023
    Veröffentlicht in Current oncology reports (01.03.2023)
    “… Purpose of Review Clonal hematopoiesis (CH) is an age-dependent process detectable using advanced sequencing technologies and is associated with multiple …”
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    Rare versus common variants in pharmacogenetics: SLCO1B1 variation and methotrexate disposition von Ramsey, Laura B, Bruun, Gitte H, Yang, Wenjian, Treviño, Lisa R, Vattathil, Selina, Scheet, Paul, Cheng, Cheng, Rosner, Gary L, Giacomini, Kathleen M, Fan, Yiping, Sparreboom, Alex, Mikkelsen, Torben S, Corydon, Thomas J, Pui, Ching-Hon, Evans, William E, Relling, Mary V

    ISSN: 1549-5469, 1549-5469
    Veröffentlicht: United States 01.01.2012
    Veröffentlicht in Genome research (01.01.2012)
    “… Methotrexate is used to treat autoimmune diseases and malignancies, including acute lymphoblastic leukemia (ALL). Inter-individual variation in clearance of …”
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