Works by Vijai, Joseph

Results: 36
    1

    Nucleotide excision repair deficiency is a targetable therapeutic vulnerability in clear cell renal cell carcinoma.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-47946-4
    By:
    • Prosz, Aurel;
    • Duan, Haohui;
    • Tisza, Viktoria;
    • Sahgal, Pranshu;
    • Topka, Sabine;
    • Klus, Gregory T.;
    • Börcsök, Judit;
    • Sztupinszki, Zsofia;
    • Hanlon, Timothy;
    • Diossy, Miklos;
    • Vizkeleti, Laura;
    • Stormoen, Dag Rune;
    • Csabai, Istvan;
    • Pappot, Helle;
    • Vijai, Joseph;
    • Offit, Kenneth;
    • Ried, Thomas;
    • Sethi, Nilay;
    • Mouw, Kent W.;
    • Spisak, Sandor
    Publication type:
    Article
    2
    3

    Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes.

    Published in:
    Briefings in Bioinformatics, 2016, v. 17, n. 4, p. 672, doi. 10.1093/bib/bbv075
    By:
    • Hart, Steven N.;
    • Maxwell, Kara N.;
    • Thomas, Tinu;
    • Ravichandran, Vignesh;
    • Wubberhorst, Bradley;
    • Klein, Robert J.;
    • Schrader, Kasmintan;
    • Szabo, Csilla;
    • Weitzel, Jeffrey N.;
    • Neuhausen, Susan L.;
    • Nathanson, Katherine;
    • Offit, Kenneth;
    • Couch, Fergus J.;
    • Vijai, Joseph
    Publication type:
    Article
    4

    Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers.

    Published in:
    Human Genetics, 2011, v. 130, n. 5, p. 685, doi. 10.1007/s00439-011-1003-z
    By:
    • Im, Kate;
    • Kirchhoff, Tomas;
    • Wang, Xianshu;
    • Green, Todd;
    • Chow, Clement;
    • Vijai, Joseph;
    • Korn, Joshua;
    • Gaudet, Mia;
    • Fredericksen, Zachary;
    • Shane Pankratz, V.;
    • Guiducci, Candace;
    • Crenshaw, Andrew;
    • McGuffog, Lesley;
    • Kartsonaki, Christiana;
    • Morrison, Jonathan;
    • Healey, Sue;
    • Sinilnikova, Olga;
    • Mai, Phuong;
    • Greene, Mark;
    • Piedmonte, Marion
    Publication type:
    Article
    5
    6

    Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genes.

    Published in:
    Human Molecular Genetics, 2021, v. 30, n. 12, p. 1142, doi. 10.1093/hmg/ddab066
    By:
    • Waller, Rosalie Griffin;
    • Klein, Robert J;
    • Vijai, Joseph;
    • McKay, James D;
    • Clay-Gilmour, Alyssa;
    • Wei, Xiaomu;
    • Madsen, Michael J;
    • Sborov, Douglas W;
    • Curtin, Karen;
    • Slager, Susan L;
    • Offit, Kenneth;
    • Vachon, Celine M;
    • Lipkin, Steven M;
    • Dumontet, Charles;
    • Camp, Nicola J
    Publication type:
    Article
    7

    Inherited variants at 3q13.33 and 3p24.1 are associated with risk of diffuse large B-cell lymphoma and implicate immune pathways.

    Published in:
    Human Molecular Genetics, 2020, v. 29, n. 1, p. 70, doi. 10.1093/hmg/ddz228
    By:
    • Kleinstern, Geffen;
    • Yan, Huihuang;
    • Hildebrandt, Michelle A T;
    • Vijai, Joseph;
    • Berndt, Sonja I;
    • Ghesquières, Hervé;
    • McKay, James;
    • Wang, Sophia S;
    • Nieters, Alexandra;
    • Ye, Yuanqing;
    • Monnereau, Alain;
    • Brooks-Wilson, Angela R;
    • Lan, Qing;
    • Melbye, Mads;
    • Jackson, Rebecca D;
    • Teras, Lauren R;
    • Purdue, Mark P;
    • Vajdic, Claire M;
    • Vermeulen, Roel C H;
    • Giles, Graham G
    Publication type:
    Article
    8

    Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-56944-1
    By:
    • Mitchell, Jonathan;
    • Camacho, Niedzica;
    • Shea, Patrick;
    • Stopsack, Konrad H.;
    • Joseph, Vijai;
    • Burren, Oliver S.;
    • Dhindsa, Ryan S.;
    • Nag, Abhishek;
    • Berchuck, Jacob E.;
    • O'Neill, Amanda;
    • Abbasi, Ali;
    • Zoghbi, Anthony W.;
    • Alegre-Díaz, Jesus;
    • Kuri-Morales, Pablo;
    • Berumen, Jaime;
    • Tapia-Conyer, Roberto;
    • Emberson, Jonathan;
    • Torres, Jason M.;
    • Collins, Rory;
    • Wang, Quanli
    Publication type:
    Article
    9

    High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation.

    Published in:
    Human Genetics, 2018, v. 137, n. 4, p. 343, doi. 10.1007/s00439-018-1886-z
    By:
    • Lencz, Todd;
    • Yu, Jin;
    • Palmer, Cameron;
    • Carmi, Shai;
    • Ben-Avraham, Danny;
    • Barzilai, Nir;
    • Bressman, Susan;
    • Darvasi, Ariel;
    • Cho, Judy H.;
    • Clark, Lorraine N.;
    • Gümüş, Zeynep H.;
    • Joseph, Vijai;
    • Klein, Robert;
    • Lipkin, Steven;
    • Offit, Kenneth;
    • Ostrer, Harry;
    • Ozelius, Laurie J.;
    • Peter, Inga;
    • Atzmon, Gil;
    • Pe’er, Itsik
    Publication type:
    Article
    10

    Author Correction: The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.

    Published in:
    2017
    By:
    • Slavin, Thomas P.;
    • Maxwell, Kara N.;
    • Lilyquist, Jenna;
    • Vijai, Joseph;
    • Neuhausen, Susan L.;
    • Hart, Steve N.;
    • Ravichandran, Vignesh;
    • Thomas, Tinu;
    • Maria, Ann;
    • Villano, Danylo;
    • Schrader, Kasmintan A.;
    • Moore, Raymond;
    • Hu, Chunling;
    • Wubbenhorst, Bradley;
    • Wenz, Brandon M.;
    • D'Andrea, Kurt;
    • Robson, Mark E.;
    • Peterlongo, Paolo;
    • Bonanni, Bernardo;
    • Ford, James M.
    Publication type:
    Correction Notice
    11

    The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.

    Published in:
    NPJ Breast Cancer, 2017, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41523-017-0024-8
    By:
    • Slavin, Thomas P.;
    • Maxwell, Kara N.;
    • Lilyquist, Jenna;
    • Vijai, Joseph;
    • Neuhausen, Susan L.;
    • Hart, Steven N.;
    • Ravichandran, Vignesh;
    • Thomas, Tinu;
    • Maria, Ann;
    • Villano, Danylo;
    • Schrader, Kasmintan A.;
    • Moore, Raymond;
    • Hu, Chunling;
    • Wubbenhorst, Bradley;
    • Wenz, Brandon M.;
    • D'Andrea, Kurt;
    • Robson, Mark E.;
    • Peterlongo, Paolo;
    • Bonanni, Bernardo;
    • Ford, James M.
    Publication type:
    Article
    12

    Genetic susceptibility to diffuse large B-cell lymphoma in a pooled study of three Eastern Asian populations.

    Published in:
    European Journal of Haematology, 2015, v. 95, n. 5, p. 442, doi. 10.1111/ejh.12513
    By:
    • Bassig, Bryan A.;
    • Cerhan, James R.;
    • Au, Wing‐Yan;
    • Kim, Hee Nam;
    • Sangrajrang, Suleeporn;
    • Hu, Wei;
    • Tse, Jovic;
    • Berndt, Sonja;
    • Zheng, Tongzhang;
    • Zhang, Heping;
    • Pornsopone, Pattarapong;
    • Lee, Je‐Jung;
    • Kim, Hyeoung‐Joon;
    • Skibola, Christine F.;
    • Vijai, Joseph;
    • Burdette, Laurie;
    • Yeager, Meredith;
    • Brennan, Paul;
    • Shin, Min‐Ho;
    • Liang, Raymond
    Publication type:
    Article
    13
    14
    15

    Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

    Published in:
    PLoS Genetics, 2018, v. 14, n. 2, p. 1, doi. 10.1371/journal.pgen.1007111
    By:
    • Waller, Rosalie G.;
    • Darlington, Todd M.;
    • Wei, Xiaomu;
    • Madsen, Michael J.;
    • Thomas, Alun;
    • Curtin, Karen;
    • Coon, Hilary;
    • Rajamanickam, Venkatesh;
    • Musinsky, Justin;
    • Jayabalan, David;
    • Atanackovic, Djordje;
    • Rajkumar, S. Vincent;
    • Kumar, Shaji;
    • Slager, Susan;
    • Middha, Mridu;
    • Galia, Perrine;
    • Demangel, Delphine;
    • Salama, Mohamed;
    • Joseph, Vijai;
    • McKay, James
    Publication type:
    Article
    16
    17

    Genetically Determined Height and Risk of Non-hodgkin Lymphoma.

    Published in:
    Frontiers in Oncology, 2020, v. 10, p. 1, doi. 10.3389/fonc.2019.01539
    By:
    • Moore, Amy;
    • Kane, Eleanor;
    • Wang, Zhaoming;
    • Panagiotou, Orestis A.;
    • Teras, Lauren R.;
    • Monnereau, Alain;
    • Wong Doo, Nicole;
    • Machiela, Mitchell J.;
    • Skibola, Christine F.;
    • Slager, Susan L.;
    • Salles, Gilles;
    • Camp, Nicola J.;
    • Bracci, Paige M.;
    • Nieters, Alexandra;
    • Vermeulen, Roel C. H.;
    • Vijai, Joseph;
    • Smedby, Karin E.;
    • Zhang, Yawei;
    • Vajdic, Claire M.;
    • Cozen, Wendy
    Publication type:
    Article
    18

    Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia.

    Published in:
    Nature Communications, 2017, v. 8, n. 2, p. 14175, doi. 10.1038/ncomms14175
    By:
    • Law, Philip J.;
    • Berndt, Sonja I.;
    • Speedy, Helen E.;
    • Camp, Nicola J.;
    • Sava, Georgina P.;
    • Skibola, Christine F.;
    • Holroyd, Amy;
    • Joseph, Vijai;
    • Sunter, Nicola J.;
    • Nieters, Alexandra;
    • Bea, Silvia;
    • Monnereau, Alain;
    • Martin-Garcia, David;
    • Goldin, Lynn R.;
    • Clot, Guillem;
    • Teras, Lauren R.;
    • Quintela, Inés;
    • Birmann, Brenda M.;
    • Jayne, Sandrine;
    • Cozen, Wendy
    Publication type:
    Article
    19

    Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.

    Published in:
    Nature Communications, 2016, v. 7, n. 3, p. 10933, doi. 10.1038/ncomms10933
    By:
    • Berndt, Sonja I.;
    • Camp, Nicola J.;
    • Skibola, Christine F.;
    • Vijai, Joseph;
    • Wang, Zhaoming;
    • Gu, Jian;
    • Nieters, Alexandra;
    • Kelly, Rachel S.;
    • Smedby, Karin E.;
    • Monnereau, Alain;
    • Cozen, Wendy;
    • Cox, Angela;
    • Wang, Sophia S.;
    • Lan, Qing;
    • Teras, Lauren R.;
    • Machado, Moara;
    • Yeager, Meredith;
    • Brooks-Wilson, Angela R.;
    • Hartge, Patricia;
    • Purdue, Mark P.
    Publication type:
    Article
    20

    A genome-wide association study of marginal zone lymphoma shows association to the HLA region.

    Published in:
    Nature Communications, 2015, v. 6, n. 1, p. 5751, doi. 10.1038/ncomms6751
    By:
    • Vijai, Joseph;
    • Wang, Zhaoming;
    • Berndt, Sonja I.;
    • Skibola, Christine F.;
    • Slager, Susan L.;
    • de Sanjose, Silvia;
    • Melbye, Mads;
    • Glimelius, Bengt;
    • Bracci, Paige M.;
    • Conde, Lucia;
    • Birmann, Brenda M.;
    • Wang, Sophia S.;
    • Brooks-Wilson, Angela R.;
    • Lan, Qing;
    • de Bakker, Paul I. W.;
    • Vermeulen, Roel C. H.;
    • Portlock, Carol;
    • Ansell, Stephen M.;
    • Link, Brian K.;
    • Riby, Jacques
    Publication type:
    Article
    21

    Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.

    Published in:
    Nature Communications, 2014, v. 5, n. 9, p. 4835, doi. 10.1038/ncomms5835
    By:
    • Carmi, Shai;
    • Hui, Ken Y.;
    • Kochav, Ethan;
    • Liu, Xinmin;
    • Xue, James;
    • Grady, Fillan;
    • Guha, Saurav;
    • Upadhyay, Kinnari;
    • Ben-Avraham, Dan;
    • Mukherjee, Semanti;
    • Bowen, B. Monica;
    • Thomas, Tinu;
    • Vijai, Joseph;
    • Cruts, Marc;
    • Froyen, Guy;
    • Lambrechts, Diether;
    • Plaisance, Stéphane;
    • Van Broeckhoven, Christine;
    • Van Damme, Philip;
    • Van Marck, Herwig
    Publication type:
    Article
    22
    23

    Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes.

    Published in:
    Human Molecular Genetics, 2016, v. 25, n. 8, p. 1663, doi. 10.1093/hmg/ddw027
    By:
    • Machiela, Mitchell J.;
    • Qing Lan;
    • Slager, Susan L.;
    • Vermeulen, Roel C.H.;
    • Teras, Lauren R.;
    • Camp, Nicola J.;
    • Cerhan, James R.;
    • Spinelli, John J.;
    • Wang, Sophia S.;
    • Nieters, Alexandra;
    • Vijai, Joseph;
    • Yeager, Meredith;
    • Zhaoming Wang;
    • Ghesquières, Hervé;
    • McKay, James;
    • Conde, Lucia;
    • de Bakker, Paul I. W.;
    • Cox, David G.;
    • Burdett, Laurie;
    • Monnereau, Alain
    Publication type:
    Article
    24

    Mutation Detection in Patients With Advanced Cancer by Universal Sequencing of Cancer-Related Genes in Tumor and Normal DNA vs Guideline-Based Germline Testing.

    Published in:
    2017
    By:
    • Mandelker, Diana;
    • Liying Zhang;
    • Kemel, Yelena;
    • Stadler, Zsofia K.;
    • Joseph, Vijai;
    • Zehir, Ahmet;
    • Pradhan, Nisha;
    • Arnold, Angela;
    • Walsh, Michael F.;
    • Yirong Li;
    • Balakrishnan, Anoop R.;
    • Syed, Aijazuddin;
    • Prasad, Meera;
    • Nafa, Khedoudja;
    • Carlo, Maria I.;
    • Cadoo, Karen A.;
    • Sheehan, Meg;
    • Fleischut, Megan H.;
    • Salo-Mullen, Erin;
    • Trottier, Magan
    Publication type:
    journal article
    25

    A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis.

    Published in:
    PLoS ONE, 2016, v. 11, n. 1, p. 1, doi. 10.1371/journal.pone.0146435
    By:
    • Markowitz, Sanford D.;
    • Nock, Nora L.;
    • Schmit, Stephanie L.;
    • Stadler, Zsofia K.;
    • Joseph, Vijai;
    • Zhang, Lu;
    • Willis, Joseph E.;
    • Scacheri, Peter;
    • Veigl, Martina;
    • Adams, Mark D.;
    • Raskin, Leon;
    • Sullivan, John F.;
    • Stratton, Kelly;
    • Shia, Jinru;
    • Ellis, Nathan;
    • Rennert, Hedy S.;
    • Manschreck, Christopher;
    • Li, Li;
    • Offit, Kenneth;
    • Elston, Robert C.
    Publication type:
    Article
    26
    27

    Genetic Variation in DNA Repair Pathways and Risk of Non-Hodgkin's Lymphoma.

    Published in:
    PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0101685
    By:
    • Rendleman, Justin;
    • Antipin, Yevgeniy;
    • Reva, Boris;
    • Adaniel, Christina;
    • Przybylo, Jennifer A.;
    • Dutra-Clarke, Ana;
    • Hansen, Nichole;
    • Heguy, Adriana;
    • Huberman, Kety;
    • Borsu, Laetitia;
    • Paltiel, Ora;
    • Ben-Yehuda, Dina;
    • Brown, Jennifer R.;
    • Freedman, Arnold S.;
    • Sander, Chris;
    • Zelenetz, Andrew;
    • Klein, Robert J.;
    • Shao, Yongzhao;
    • Lacher, Mortimer;
    • Vijai, Joseph
    Publication type:
    Article
    28
    29

    Assessment of <i>SLX4</i> Mutations in Hereditary Breast Cancers.

    Published in:
    PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066961
    By:
    • Shah, Sohela;
    • Kim, Yonghwan;
    • Ostrovnaya, Irina;
    • Murali, Rajmohan;
    • Schrader, Kasmintan A.;
    • Lach, Francis P.;
    • Sarrel, Kara;
    • Rau-Murthy, Rohini;
    • Hansen, Nichole;
    • Zhang, Liyng;
    • Kirchhoff, Tomas;
    • Stadler, Zsofia;
    • Robson, Mark;
    • Vijai, Joseph;
    • Offit, Kenneth;
    • Smogorzewska, Agata
    Publication type:
    Article
    30

    Germline ETV6 Mutations Confer Susceptibility to Acute Lymphoblastic Leukemia and Thrombocytopenia.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 6, p. 1, doi. 10.1371/journal.pgen.1005262
    By:
    • Topka, Sabine;
    • Vijai, Joseph;
    • Walsh, Michael F.;
    • Jacobs, Lauren;
    • Maria, Ann;
    • Villano, Danylo;
    • Gaddam, Pragna;
    • Wu, Gang;
    • McGee, Rose B.;
    • Quinn, Emily;
    • Inaba, Hiroto;
    • Hartford, Christine;
    • Pui, Ching-hon;
    • Pappo, Alberto;
    • Edmonson, Michael;
    • Zhang, Michael Y.;
    • Stepensky, Polina;
    • Steinherz, Peter;
    • Schrader, Kasmintan;
    • Lincoln, Anne
    Publication type:
    Article
    31

    A Recessive Founder Mutation in Regulator of Telomere Elongation Helicase 1, <i>RTEL1</i>, Underlies Severe Immunodeficiency and Features of Hoyeraal Hreidarsson Syndrome.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 8, p. 1, doi. 10.1371/journal.pgen.1003695
    By:
    • Ballew, Bari J.;
    • Joseph, Vijai;
    • De, Saurav;
    • Sarek, Grzegorz;
    • Vannier, Jean-Baptiste;
    • Stracker, Travis;
    • Schrader, Kasmintan A.;
    • Small, Trudy N.;
    • O'Reilly, Richard;
    • Manschreck, Chris;
    • Harlan Fleischut, Megan M.;
    • Zhang, Liying;
    • Sullivan, John;
    • Stratton, Kelly;
    • Yeager, Meredith;
    • Jacobs, Kevin;
    • Giri, Neelam;
    • Alter, Blanche P.;
    • Boland, Joseph;
    • Burdett, Laurie
    Publication type:
    Article
    32

    Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 3, p. 1, doi. 10.1371/journal.pgen.1003173
    By:
    • Gaudet, Mia M.;
    • Kuchenbaecker, Karoline B.;
    • Vijai, Joseph;
    • Klein, Robert J.;
    • Kirchhoff, Tomas;
    • McGuffog, Lesley;
    • Barrowdale, Daniel;
    • Dunning, Alison M.;
    • Lee, Andrew;
    • Dennis, Joe;
    • Healey, Sue;
    • Dicks, Ed;
    • Soucy, Penny;
    • Sinilnikova, Olga M.;
    • Pankratz, Vernon S.;
    • Xianshu Wang;
    • Eldridge, Ronald C.;
    • Tessier, Daniel C.;
    • Vincent, Daniel;
    • Bacot, Francois
    Publication type:
    Article
    33

    Susceptibility Loci Associated with Specific and Shared Subtypes of Lymphoid Malignancies.

    Published in:
    PLoS Genetics, 2013, v. 9, n. 1, p. 1, doi. 10.1371/journal.pgen.1003220
    By:
    • Vijai, Joseph;
    • Kirchhoff, Tomas;
    • Schrader, Kasmintan A.;
    • Brown, Jennifer;
    • Dutra-Clarke, Ana Virginia;
    • Manschreck, Christopher;
    • Hansen, Nichole;
    • Rau-Murthy, Rohini;
    • Sarrel, Kara;
    • Przybylo, Jennifer;
    • Shah, Sohela;
    • Cheguri, Srujana;
    • Stadler, Zsofia;
    • Liying Zhang;
    • Paltiel, Ora;
    • Ben-Yehuda, Dina;
    • Viale, Agnes;
    • Portlock, Carol;
    • Straus, David;
    • Lipkin, Steven M.
    Publication type:
    Article
    34

    A recurrent germline PAX5 mutation confers susceptibility to pre-B cell acute lymphoblastic leukemia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 10, p. 1226, doi. 10.1038/ng.2754
    By:
    • Shah, Sohela;
    • Schrader, Kasmintan A;
    • Waanders, Esmé;
    • Timms, Andrew E;
    • Vijai, Joseph;
    • Miething, Cornelius;
    • Wechsler, Jeremy;
    • Yang, Jun;
    • Hayes, James;
    • Klein, Robert J;
    • Zhang, Jinghui;
    • Wei, Lei;
    • Wu, Gang;
    • Rusch, Michael;
    • Nagahawatte, Panduka;
    • Ma, Jing;
    • Chen, Shann-Ching;
    • Song, Guangchun;
    • Cheng, Jinjun;
    • Meyers, Paul
    Publication type:
    Article
    35

    Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.

    Published in:
    Nature Genetics, 2013, v. 45, n. 8, p. 868, doi. 10.1038/ng.2652
    By:
    • Berndt, Sonja I;
    • Skibola, Christine F;
    • Joseph, Vijai;
    • Camp, Nicola J;
    • Nieters, Alexandra;
    • Wang, Zhaoming;
    • Cozen, Wendy;
    • Monnereau, Alain;
    • Wang, Sophia S;
    • Kelly, Rachel S;
    • Lan, Qing;
    • Teras, Lauren R;
    • Chatterjee, Nilanjan;
    • Chung, Charles C;
    • Yeager, Meredith;
    • Brooks-Wilson, Angela R;
    • Hartge, Patricia;
    • Purdue, Mark P;
    • Birmann, Brenda M;
    • Armstrong, Bruce K
    Publication type:
    Article
    36

    A Comprehensive Comparison of Early-Onset and Average-Onset Colorectal Cancers.

    Published in:
    2021
    By:
    • Cercek, Andrea;
    • Chatila, Walid K;
    • Yaeger, Rona;
    • Walch, Henry;
    • Fernandes, Gustavo Dos Santos;
    • Krishnan, Asha;
    • Palmaira, Lerie;
    • Maio, Anna;
    • Kemel, Yelena;
    • Srinivasan, Preethi;
    • Bandlamudi, Chaitanya;
    • Salo-Mullen, Erin;
    • Tejada, Prince R;
    • Belanfanti, Kimeisha;
    • Galle, Jesse;
    • Joseph, Vijai;
    • Segal, Neil;
    • Varghese, Anna;
    • Reidy-Lagunes, Diane;
    • Shia, Jinru
    Publication type:
    journal article