Works matching IS 1756994X AND DT 2022 AND VI 14 AND IP 1

Results: 163
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    Neutralization sensitivity, fusogenicity, and infectivity of Omicron subvariants.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01151-6
    By:
    • Wang, Xue-Jun;
    • Yao, Lin;
    • Zhang, Hong-Yun;
    • Zhu, Ka-Li;
    • Zhao, Jing;
    • Zhan, Bing-Dong;
    • Li, Yi-Ke;
    • He, Xue-Juan;
    • Huang, Cong;
    • Wang, Zhuang-Ye;
    • Jiang, Ming-Dong;
    • Yang, Peng;
    • Yang, Yang;
    • Wang, Guo-Lin;
    • Wang, Sheng-Qi;
    • Dai, Er-Hei;
    • Gao, Hui-Xia;
    • Ma, Mai-Juan
    Publication type:
    Article
    3

    The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01149-0
    By:
    • Stafford, Fergus;
    • Krishnan, Neesha;
    • Richardson, Ebony;
    • Butters, Alexandra;
    • Hespe, Sophie;
    • Burns, Charlotte;
    • Gray, Belinda;
    • Medi, Caroline;
    • Nowak, Natalie;
    • Isbister, Julia C.;
    • Raju, Hariharan;
    • Richmond, David;
    • Ryan, Mark P.;
    • Singer, Emma S.;
    • Sy, Raymond W.;
    • Yeates, Laura;
    • Bagnall, Richard D.;
    • Semsarian, Christopher;
    • Ingles, Jodie
    Publication type:
    Article
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    Spatiotemporal evolution of the clear cell renal cell carcinoma microenvironment links intra-tumoral heterogeneity to immune escape.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01146-3
    By:
    • Golkaram, Mahdi;
    • Kuo, Fengshen;
    • Gupta, Sounak;
    • Carlo, Maria I.;
    • Salmans, Michael L.;
    • Vijayaraghavan, Raakhee;
    • Tang, Cerise;
    • Makarov, Vlad;
    • Rappold, Phillip;
    • Blum, Kyle A.;
    • Zhao, Chen;
    • Mehio, Rami;
    • Zhang, Shile;
    • Godsey, Jim;
    • Pawlowski, Traci;
    • DiNatale, Renzo G.;
    • Morris, Luc G. T.;
    • Durack, Jeremy;
    • Russo, Paul;
    • Kotecha, Ritesh R.
    Publication type:
    Article
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    Loss of Y in leukocytes as a risk factor for critical COVID-19 in men.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01144-5
    By:
    • Bruhn-Olszewska, Bożena;
    • Davies, Hanna;
    • Sarkisyan, Daniil;
    • Juhas, Ulana;
    • Rychlicka-Buniowska, Edyta;
    • Wójcik, Magdalena;
    • Horbacz, Monika;
    • Jąkalski, Marcin;
    • Olszewski, Paweł;
    • Westholm, Jakub O.;
    • Smialowska, Agata;
    • Wierzba, Karol;
    • Torinsson Naluai, Åsa;
    • Jern, Niklas;
    • Andersson, Lars-Magnus;
    • Järhult, Josef D.;
    • Filipowicz, Natalia;
    • Tiensuu Janson, Eva;
    • Rubertsson, Sten;
    • Lipcsey, Miklós
    Publication type:
    Article
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    Epigenetic and transcriptomic reprogramming in monocytes of severe COVID-19 patients reflects alterations in myeloid differentiation and the influence of inflammatory cytokines.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01137-4
    By:
    • Godoy-Tena, Gerard;
    • Barmada, Anis;
    • Morante-Palacios, Octavio;
    • de la Calle-Fabregat, Carlos;
    • Martins-Ferreira, Ricardo;
    • Ferreté-Bonastre, Anna G.;
    • Ciudad, Laura;
    • Ruiz-Sanmartín, Adolfo;
    • Martínez-Gallo, Mónica;
    • Ferrer, Ricard;
    • Ruiz-Rodriguez, Juan Carlos;
    • Rodríguez-Ubreva, Javier;
    • Vento-Tormo, Roser;
    • Ballestar, Esteban
    Publication type:
    Article
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    Ganciclovir-induced mutations are present in a diverse spectrum of post-transplant malignancies.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01131-w
    By:
    • Fang, Hu;
    • Yan, Helen H. N.;
    • Bilardi, Rebecca A.;
    • Flensburg, Christoffer;
    • Yang, Haocheng;
    • Barbour, Jayne A.;
    • Siu, Hoi Cheong;
    • Turski, Michelle;
    • Chew, Edward;
    • Xu, Zhen;
    • Lam, Siu T.;
    • Sharma, Rakesh;
    • Xu, Mengya;
    • Li, Junshi;
    • Ip, Ho W.;
    • Cheung, Carol Y. M.;
    • Huen, Michael S. Y.;
    • Sweet-Cordero, E. Alejandro;
    • Majewski, Ian J.;
    • Leung, Suet Y.
    Publication type:
    Article
    22

    Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01106-x
    By:
    • Johnson, Ruth;
    • Ding, Yi;
    • Venkateswaran, Vidhya;
    • Bhattacharya, Arjun;
    • Boulier, Kristin;
    • Chiu, Alec;
    • Knyazev, Sergey;
    • Schwarz, Tommer;
    • Freund, Malika;
    • Zhan, Lingyu;
    • Burch, Kathryn S.;
    • Caggiano, Christa;
    • Hill, Brian;
    • Rakocz, Nadav;
    • Balliu, Brunilda;
    • Denny, Christopher T.;
    • Sul, Jae Hoon;
    • Zaitlen, Noah;
    • Arboleda, Valerie A.;
    • Halperin, Eran
    Publication type:
    Article
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    Genomic and transcriptomic analysis of a diffuse pleural mesothelioma patient-derived xenograft library.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01129-4
    By:
    • Offin, Michael;
    • Sauter, Jennifer L.;
    • Tischfield, Sam E.;
    • Egger, Jacklynn V.;
    • Chavan, Shweta;
    • Shah, Nisargbhai S.;
    • Manoj, Parvathy;
    • Ventura, Katia;
    • Allaj, Viola;
    • de Stanchina, Elisa;
    • Travis, William;
    • Ladanyi, Marc;
    • Rimner, Andreas;
    • Rusch, Valerie W.;
    • Adusumilli, Prasad S.;
    • Poirier, John T.;
    • Zauderer, Marjorie G.;
    • Rudin, Charles M.;
    • Sen, Triparna
    Publication type:
    Article
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    Author Correction: Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative.

    Published in:
    2022
    By:
    • Johnson, Ruth;
    • Ding, Yi;
    • Venkateswaran, Vidhya;
    • Bhattacharya, Arjun;
    • Boulier, Kristin;
    • Chiu, Alec;
    • Knyazev, Sergey;
    • Schwarz, Tommer;
    • Freund, Malika;
    • Zhan, Lingyu;
    • Burch, Kathryn S.;
    • Caggiano, Christa;
    • Hill, Brian;
    • Rakocz, Nadav;
    • Balliu, Brunilda;
    • Denny, Christopher T.;
    • Sul, Jae Hoon;
    • Zaitlen, Noah;
    • Arboleda, Valerie A.;
    • Halperin, Eran
    Publication type:
    Correction Notice
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    The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01123-w
    By:
    • Du, Haowei;
    • Jolly, Angad;
    • Grochowski, Christopher M.;
    • Yuan, Bo;
    • Dawood, Moez;
    • Jhangiani, Shalini N.;
    • Li, He;
    • Muzny, Donna;
    • Fatih, Jawid M.;
    • Coban-Akdemir, Zeynep;
    • Carlin, Mary Esther;
    • Scheuerle, Angela E.;
    • Witzl, Karin;
    • Posey, Jennifer E.;
    • Pendleton, Matthew;
    • Harrington, Eoghan;
    • Juul, Sissel;
    • Hastings, P. J.;
    • Bi, Weimin;
    • Gibbs, Richard A.
    Publication type:
    Article
    30

    Computational quantification and characterization of independently evolving cellular subpopulations within tumors is critical to inhibit anti-cancer therapy resistance.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01121-y
    By:
    • Alkhatib, Heba;
    • Rubinstein, Ariel M.;
    • Vasudevan, Swetha;
    • Flashner-Abramson, Efrat;
    • Stefansky, Shira;
    • Chowdhury, Sangita Roy;
    • Oguche, Solomon;
    • Peretz-Yablonsky, Tamar;
    • Granit, Avital;
    • Granot, Zvi;
    • Ben-Porath, Ittai;
    • Sheva, Kim;
    • Feldman, Jon;
    • Cohen, Noa E.;
    • Meirovitz, Amichay;
    • Kravchenko-Balasha, Nataly
    Publication type:
    Article
    31

    DNA methylome-wide association study of genetic risk for depression implicates antigen processing and immune responses.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01039-5
    By:
    • Shen, Xueyi;
    • Caramaschi, Doretta;
    • Adams, Mark J.;
    • Walker, Rosie M.;
    • Min, Josine L.;
    • Kwong, Alex;
    • Hemani, Gibran;
    • Barbu, Miruna C.;
    • Whalley, Heather C.;
    • Harris, Sarah E.;
    • Deary, Ian J.;
    • Morris, Stewart W.;
    • Cox, Simon R.;
    • Relton, Caroline L.;
    • Marioni, Riccardo E.;
    • Evans, Kathryn L.;
    • McIntosh, Andrew M.
    Publication type:
    Article
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    Mendelian gene identification through mouse embryo viability screening.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01118-7
    By:
    • Cacheiro, Pilar;
    • Westerberg, Carl Henrik;
    • Mager, Jesse;
    • Dickinson, Mary E.;
    • Nutter, Lauryl M. J.;
    • Muñoz-Fuentes, Violeta;
    • Hsu, Chih-Wei;
    • Van den Veyver, Ignatia B.;
    • Flenniken, Ann M.;
    • McKerlie, Colin;
    • Murray, Stephen A.;
    • Teboul, Lydia;
    • Heaney, Jason D.;
    • Lloyd, K. C. Kent;
    • Lanoue, Louise;
    • Braun, Robert E.;
    • White, Jacqueline K.;
    • Creighton, Amie K.;
    • Laurin, Valerie;
    • Guo, Ruolin
    Publication type:
    Article
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    Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01117-8
    By:
    • Lewis, Anna C. F.;
    • Perez, Emma F.;
    • Prince, Anya E. R.;
    • Flaxman, Hana R.;
    • Gomez, Lizbeth;
    • Brockman, Deanna G.;
    • Chandler, Paulette D.;
    • Kerman, Benjamin J.;
    • Lebo, Matthew S.;
    • Smoller, Jordan W.;
    • Weiss, Scott T.;
    • Blout Zawatksy, Carrie L.;
    • Meigs, James B.;
    • Green, Robert C.;
    • Vassy, Jason L.;
    • Karlson, Elizabeth W.
    Publication type:
    Article
    38

    Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01113-y
    By:
    • Yuan, Bo;
    • Schulze, Katharina V.;
    • Assia Batzir, Nurit;
    • Sinson, Jefferson;
    • Dai, Hongzheng;
    • Zhu, Wenmiao;
    • Bocanegra, Francia;
    • Fong, Chin-To;
    • Holder, Jimmy;
    • Nguyen, Joanne;
    • Schaaf, Christian P.;
    • Yang, Yaping;
    • Bi, Weimin;
    • Eng, Christine;
    • Shaw, Chad;
    • Lupski, James R.;
    • Liu, Pengfei
    Publication type:
    Article
    39

    African-specific alleles modify risk for asthma at the 17q12-q21 locus in African Americans.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01114-x
    By:
    • Washington III, Charles;
    • Dapas, Matthew;
    • Biddanda, Arjun;
    • Magnaye, Kevin M.;
    • Aneas, Ivy;
    • Helling, Britney A.;
    • Szczesny, Brooke;
    • Boorgula, Meher Preethi;
    • Taub, Margaret A.;
    • Kenny, Eimear;
    • Mathias, Rasika A.;
    • Barnes, Kathleen C.;
    • CAAPA;
    • Campbell, Monica;
    • Figueiredo, Camila;
    • Hansel, Nadia N.;
    • Ober, Carole;
    • Olopade, Christopher O.;
    • Rotimi, Charles N.;
    • Watson, Harold
    Publication type:
    Article
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    Longitudinal multi-omics analysis identifies early blood-based predictors of anti-TNF therapy response in inflammatory bowel disease.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01112-z
    By:
    • Mishra, Neha;
    • Aden, Konrad;
    • Blase, Johanna I.;
    • Baran, Nathan;
    • Bordoni, Dora;
    • Tran, Florian;
    • Conrad, Claudio;
    • Avalos, Diana;
    • Jaeckel, Charlot;
    • Scherer, Michael;
    • Sørensen, Signe B.;
    • Overgaard, Silja H.;
    • Schulte, Berenice;
    • Nikolaus, Susanna;
    • Rey, Guillaume;
    • Gasparoni, Gilles;
    • Lyons, Paul A.;
    • Schultze, Joachim L.;
    • Walter, Jörn;
    • Andersen, Vibeke
    Publication type:
    Article
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    Intratumor heterogeneity and T cell exhaustion in primary CNS lymphoma.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01110-1
    By:
    • Heming, Michael;
    • Haessner, Svea;
    • Wolbert, Jolien;
    • Lu, I-Na;
    • Li, Xiaolin;
    • Brokinkel, Benjamin;
    • Müther, Michael;
    • Holling, Markus;
    • Stummer, Walter;
    • Thomas, Christian;
    • Schulte-Mecklenbeck, Andreas;
    • de Faria, Flavia;
    • Stoeckius, Marlon;
    • Hailfinger, Stephan;
    • Lenz, Georg;
    • Kerl, Kornelius;
    • Wiendl, Heinz;
    • Meyer zu Hörste, Gerd;
    • Grauer, Oliver M.
    Publication type:
    Article
    44

    Correction: Rapid molecular diagnostics of tuberculosis resistance by targeted stool sequencing.

    Published in:
    2022
    By:
    • Sibandze, Doctor B.;
    • Kay, Alexander;
    • Dreyer, Viola;
    • Sikhondze, Welile;
    • Dlamini, Qiniso;
    • DiNardo, Andrew;
    • Mtetwa, Godwin;
    • Lukhele, Bhekumusa;
    • Vambe, Debrah;
    • Lange, Christoph;
    • Dlamini, Muyalo Glenn;
    • Ness, Tara;
    • Mejia, Rojelio;
    • Kalsdorf, Barbara;
    • Heyckendorf, Jan;
    • Kuhns, Martin;
    • Maurer, Florian P.;
    • Dlamini, Sindisiwe;
    • Maphalala, Gugu;
    • Niemann, Stefan
    Publication type:
    Correction Notice
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    A novel molecular signature identifies mixed subtypes in renal cell carcinoma with poor prognosis and independent response to immunotherapy.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01105-y
    By:
    • Büttner, Florian A.;
    • Winter, Stefan;
    • Stühler, Viktoria;
    • Rausch, Steffen;
    • Hennenlotter, Jörg;
    • Füssel, Susanne;
    • Zastrow, Stefan;
    • Meinhardt, Matthias;
    • Toma, Marieta;
    • Jerónimo, Carmen;
    • Henrique, Rui;
    • Miranda-Gonçalves, Vera;
    • Kröger, Nils;
    • Ribback, Silvia;
    • Hartmann, Arndt;
    • Agaimy, Abbas;
    • Stöhr, Christine;
    • Polifka, Iris;
    • Fend, Falko;
    • Scharpf, Marcus
    Publication type:
    Article
    47

    Single-cell transcriptomics reveals common epithelial response patterns in human acute kidney injury.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01108-9
    By:
    • Hinze, Christian;
    • Kocks, Christine;
    • Leiz, Janna;
    • Karaiskos, Nikos;
    • Boltengagen, Anastasiya;
    • Cao, Shuang;
    • Skopnik, Christopher Mark;
    • Klocke, Jan;
    • Hardenberg, Jan-Hendrik;
    • Stockmann, Helena;
    • Gotthardt, Inka;
    • Obermayer, Benedikt;
    • Haghverdi, Laleh;
    • Wyler, Emanuel;
    • Landthaler, Markus;
    • Bachmann, Sebastian;
    • Hocke, Andreas C.;
    • Corman, Victor;
    • Busch, Jonas;
    • Schneider, Wolfgang
    Publication type:
    Article
    48

    Integrative genomic and transcriptomic analyses illuminate the ontology of HER2-low breast carcinomas.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01104-z
    By:
    • Berrino, Enrico;
    • Annaratone, Laura;
    • Bellomo, Sara Erika;
    • Ferrero, Giulio;
    • Gagliardi, Amedeo;
    • Bragoni, Alberto;
    • Grassini, Dora;
    • Guarrera, Simonetta;
    • Parlato, Caterina;
    • Casorzo, Laura;
    • Panero, Mara;
    • Sarotto, Ivana;
    • Giordano, Silvia;
    • Cereda, Matteo;
    • Montemurro, Filippo;
    • Ponzone, Riccardo;
    • Crosetto, Nicola;
    • Naccarati, Alessio;
    • Sapino, Anna;
    • Marchiò, Caterina
    Publication type:
    Article
    49

    Accumulation of copy number alterations and clinical progression across advanced prostate cancer.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01080-4
    By:
    • Grist, Emily;
    • Friedrich, Stefanie;
    • Brawley, Christopher;
    • Mendes, Larissa;
    • Parry, Marina;
    • Ali, Adnan;
    • Haran, Aine;
    • Hoyle, Alex;
    • Gilson, Claire;
    • Lall, Sharanpreet;
    • Zakka, Leila;
    • Bautista, Carla;
    • Landless, Alex;
    • Nowakowska, Karolina;
    • Wingate, Anna;
    • Wetterskog, Daniel;
    • Hasan, A. M. Mahedi;
    • Akato, Nafisah B.;
    • Richmond, Malissa;
    • Ishaq, Sofeya
    Publication type:
    Article
    50

    Genome-wide interrogation of structural variation reveals novel African-specific prostate cancer oncogenic drivers.

    Published in:
    Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01096-w
    By:
    • Gong, Tingting;
    • Jaratlerdsiri, Weerachai;
    • Jiang, Jue;
    • Willet, Cali;
    • Chew, Tracy;
    • Patrick, Sean M.;
    • Lyons, Ruth J.;
    • Haynes, Anne-Maree;
    • Pasqualim, Gabriela;
    • Brum, Ilma Simoni;
    • Stricker, Phillip D.;
    • Mutambirwa, Shingai B. A.;
    • Sadsad, Rosemarie;
    • Papenfuss, Anthony T.;
    • Bornman, Riana M. S.;
    • Chan, Eva K. F.;
    • Hayes, Vanessa M.
    Publication type:
    Article