Works by Guo, Yiran


Results: 83
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    BAHCC1 binds H4K20me1 to facilitate the MCM complex loading and DNA replication.

    Published in:
    Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-61284-1
    By:
    • Li, Dongxu;
    • Zhang, Zhi-Min;
    • Mei, Liu;
    • Yu, Yao;
    • Guo, Yiran;
    • Mackintosh, Samuel G.;
    • Chen, Jianbin;
    • Allison, David F.;
    • Kim, Arum;
    • Storey, Aaron J.;
    • Edmondson, Ricky D.;
    • Byrum, Stephanie D.;
    • Tackett, Alan J.;
    • Cai, Ling;
    • Cook, Jeanette G.;
    • Song, Jikui;
    • Wang, Gang Greg
    Publication type:
    Article
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    Multiparametric MRI along with machine learning predicts prognosis and treatment response in pediatric low-grade glioma.

    Published in:
    Nature Communications, 2025, v. 16, p. 1, doi. 10.1038/s41467-024-55659-z
    By:
    • Fathi Kazerooni, Anahita;
    • Kraya, Adam;
    • Rathi, Komal S.;
    • Kim, Meen Chul;
    • Vossough, Arastoo;
    • Khalili, Nastaran;
    • Familiar, Ariana M.;
    • Gandhi, Deep;
    • Khalili, Neda;
    • Kesherwani, Varun;
    • Haldar, Debanjan;
    • Anderson, Hannah;
    • Jin, Run;
    • Mahtabfar, Aria;
    • Bagheri, Sina;
    • Guo, Yiran;
    • Li, Qi;
    • Huang, Xiaoyan;
    • Zhu, Yuankun;
    • Sickler, Alex
    Publication type:
    Article
    8

    The diploid genome sequence of an Asian individual.

    Published in:
    Nature, 2008, v. 456, n. 7218, p. 60, doi. 10.1038/nature07484
    By:
    • Wang, Jun;
    • Wei Wang;
    • Ruiqiang Li;
    • Yingrui Li;
    • Geng Tian;
    • Goodman, Laurie;
    • Wei Fan;
    • Junqing Zhang;
    • Li, Jun;
    • Juanbin Zhang;
    • Yiran Guo;
    • Binxiao Feng;
    • Heng Li;
    • Yao Lu;
    • Xiaodong Fang;
    • Huiqing Liang;
    • Zhenglin Du;
    • Dong Li;
    • Yiqing Zhao;
    • Yujie Hu
    Publication type:
    Article
    9

    TreeFam: 2008 Update.

    Published in:
    Nucleic Acids Research, 2008, v. 36, p. D735
    By:
    • Ruan, Jue;
    • Li, Heng;
    • Chen, Zhongzhong;
    • Coghlan, Avril;
    • Coin, Lachlan James M.;
    • Guo, Yiran;
    • Hériché, Jean-Karim;
    • Hu, Yafeng;
    • Kristiansen, Karsten;
    • Li, Ruiqiang;
    • Liu, Tao;
    • Moses, Alan;
    • Qin, Junjie;
    • Vang, Søren;
    • Vilella, Albert J.;
    • Ureta-Vidal, Abel;
    • Bolund, Lars;
    • Wang, Jun;
    • Durbin, Richard
    Publication type:
    Article
    10

    PigGIS: Pig Genomic Informatics System.

    Published in:
    Nucleic Acids Research, 2007, v. 35, p. d654, doi. 10.1093/nar/gkl808
    By:
    • Ruan, Jue;
    • Guo, Yiran;
    • Li, Heng;
    • Hu, Yafeng;
    • Song, Fei;
    • Huang, Xin;
    • Kristiensen, Karsten;
    • Bolund, Lars;
    • Wang, Jun
    Publication type:
    Article
    11

    DNMT1 reads heterochromatic H4K20me3 to reinforce LINE-1 DNA methylation.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22665-4
    By:
    • Ren, Wendan;
    • Fan, Huitao;
    • Grimm, Sara A.;
    • Kim, Jae Jin;
    • Li, Linhui;
    • Guo, Yiran;
    • Petell, Christopher James;
    • Tan, Xiao-Feng;
    • Zhang, Zhi-Min;
    • Coan, John P.;
    • Yin, Jiekai;
    • Kim, Dae In;
    • Gao, Linfeng;
    • Cai, Ling;
    • Khudaverdyan, Nelli;
    • Çetin, Burak;
    • Patel, Dinshaw J.;
    • Wang, Yinsheng;
    • Cui, Qiang;
    • Strahl, Brian D.
    Publication type:
    Article
    12

    ANKRD11 variants: KBG syndrome and beyond.

    Published in:
    Clinical Genetics, 2021, v. 100, n. 2, p. 187, doi. 10.1111/cge.13977
    By:
    • Parenti, Ilaria;
    • Mallozzi, Mark B.;
    • Hüning, Irina;
    • Gervasini, Cristina;
    • Kuechler, Alma;
    • Agolini, Emanuele;
    • Albrecht, Beate;
    • Baquero‐Montoya, Carolina;
    • Bohring, Axel;
    • Bramswig, Nuria C.;
    • Busche, Andreas;
    • Dalski, Andreas;
    • Guo, Yiran;
    • Hanker, Britta;
    • Hellenbroich, Yorck;
    • Horn, Denise;
    • Innes, A. Micheil;
    • Leoni, Chiara;
    • Li, Yun R.;
    • Lynch, Sally Ann
    Publication type:
    Article
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    Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes.

    Published in:
    PLoS Genetics, 2011, v. 7, n. 6, p. 1, doi. 10.1371/journal.pgen.1002134
    By:
    • Smith, Erin N.;
    • Koller, Daniel L.;
    • Panganiban, Corrie;
    • Szelinger, Szabolcs;
    • Peng Zhang;
    • Badner, Judith A.;
    • Barrett, Thomas B.;
    • Berrettini, Wade H.;
    • Bloss, Cinnamon S.;
    • Byerley, William;
    • Coryell, William;
    • Edenberg, Howard J.;
    • Foroud, Tatiana;
    • Gershon, Elliot S.;
    • Greenwood, Tiffany A.;
    • Yiran Guo;
    • Hipolito, Maria;
    • Keating, Brendan J.;
    • Lawson, William B.;
    • Chunyu Liu
    Publication type:
    Article
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    Adult-onset autosomal recessive ataxia associated with neuronal ceroid lipofuscinosis type 5 gene ( CLN5) mutations.

    Published in:
    Journal of Neurology, 2015, v. 262, n. 1, p. 173, doi. 10.1007/s00415-014-7553-y
    By:
    • Mancini, Cecilia;
    • Nassani, Stefano;
    • Guo, Yiran;
    • Chen, Yulan;
    • Giorgio, Elisa;
    • Brussino, Alessandro;
    • Di Gregorio, Eleonora;
    • Cavalieri, Simona;
    • Lo Buono, Nicola;
    • Funaro, Ada;
    • Pizio, Nicola;
    • Nmezi, Bruce;
    • Kyttala, Aija;
    • Santorelli, Filippo;
    • Padiath, Quasar;
    • Hakonarson, Hakon;
    • Zhang, Hao;
    • Brusco, Alfredo
    Publication type:
    Article
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    Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of Novel TULP1 Mutation in Leber Congenital Amaurosis.

    Published in:
    Ophthalmic Genetics, 2015, v. 36, n. 4, p. 333, doi. 10.3109/13816810.2014.886269
    By:
    • Guo, Yiran;
    • Prokudin, Ivan;
    • Yu, Cong;
    • Liang, Jinlong;
    • Xie, Yi;
    • Flaherty, Maree;
    • Tian, Lifeng;
    • Crofts, Stephanie;
    • Wang, Fengxiang;
    • Snyder, James;
    • Donaldson, Craig;
    • Abdel-Magid, Nada;
    • Vazquez, Lyam;
    • Keating, Brendan;
    • Hakonarson, Hakon;
    • Wang, Jun;
    • Jamieson, Robyn V.
    Publication type:
    Article
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    Alternative lengthening of telomeres (ALT) in pediatric high-grade gliomas can occur without ATRX mutation and is enriched in patients with pathogenic germline mismatch repair (MMR) variants.

    Published in:
    Neuro-Oncology, 2023, v. 25, n. 7, p. 1331, doi. 10.1093/neuonc/noac278
    By:
    • Stundon, Jennifer L;
    • Ijaz, Heba;
    • Gaonkar, Krutika S;
    • Kaufman, Rebecca S;
    • Jin, Run;
    • Karras, Anastasios;
    • Vaksman, Zalman;
    • Kim, Jung;
    • Corbett, Ryan J;
    • Lueder, Matthew R;
    • Miller, Daniel P;
    • Guo, Yiran;
    • Santi, Mariarita;
    • Li, Marilyn;
    • Lopez, Gonzalo;
    • Storm, Phillip B;
    • Resnick, Adam C;
    • Waanders, Angela J;
    • MacFarland, Suzanne P;
    • Stewart, Douglas R
    Publication type:
    Article
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    Expanding the phenotype of PRPS1 syndromes in females: neuropathy, hearing loss and retinopathy.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 155, doi. 10.1186/s13023-014-0190-9
    By:
    • Almoguera, Berta;
    • Sijie He;
    • Corton, Marta;
    • Fernandez-San Jose, Patricia;
    • Blanco-Kelly, Fiona;
    • López-Molina, Maria Isabel;
    • García-Sandoval, Blanca;
    • del Val, Javier;
    • Yiran Guo;
    • Lifeng Tian;
    • Xuanzhu Liu;
    • Liping Guan;
    • Torres, Rosa J.;
    • Puig, Juan G.;
    • Hakonarson, Hakon;
    • Xun Xu;
    • Keating, Brendan;
    • Ayuso, Carmen
    Publication type:
    Article
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    Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.

    Published in:
    Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00408-8
    By:
    • Xiao Chang;
    • Yan Zhao;
    • Cuiping Hou;
    • Glessner, Joseph;
    • McDaniel, Lee;
    • Diamond, Maura A.;
    • Thomas, Kelly;
    • Jin Li;
    • Zhi Wei;
    • Yichuan Liu;
    • Yiran Guo;
    • Mentch, Frank D.;
    • Haijun Qiu;
    • Cecilia Kim;
    • Evans, Perry;
    • Vaksman, Zalman;
    • Diskin, Sharon J.;
    • Attiyeh, Edward F.;
    • Sleiman, Patrick;
    • Maris, John M.
    Publication type:
    Article
    34

    Genetic sharing and heritability of paediatric age of onset autoimmune diseases.

    Published in:
    Nature Communications, 2015, v. 6, n. 10, p. 8442, doi. 10.1038/ncomms9442
    By:
    • Li, Yun R.;
    • Zhao, Sihai D.;
    • Li, Jin;
    • Bradfield, Jonathan P.;
    • Mohebnasab, Maede;
    • Steel, Laura;
    • Kobie, Julie;
    • Abrams, Debra J.;
    • Mentch, Frank D.;
    • Glessner, Joseph T.;
    • Guo, Yiran;
    • Wei, Zhi;
    • Connolly, John J.;
    • Cardinale, Christopher J.;
    • Bakay, Marina;
    • Li, Dong;
    • Maggadottir, S. Melkorka;
    • Thomas, Kelly A.;
    • Qui, Haijun;
    • Chiavacci, Rosetta M.
    Publication type:
    Article
    35

    Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndrome.

    Published in:
    Human Genetics, 2021, v. 140, n. 7, p. 1061, doi. 10.1007/s00439-021-02274-3
    By:
    • Li, Dong;
    • March, Michael E.;
    • Fortugno, Paola;
    • Cox, Liza L.;
    • Matsuoka, Leticia S.;
    • Monetta, Rosanna;
    • Seiler, Christoph;
    • Pyle, Louise C.;
    • Bedoukian, Emma C.;
    • Sánchez-Soler, María José;
    • Caluseriu, Oana;
    • Grand, Katheryn;
    • Tam, Allison;
    • Aycinena, Alicia R. P.;
    • Camerota, Letizia;
    • Guo, Yiran;
    • Sleiman, Patrick;
    • Callewaert, Bert;
    • Kumps, Candy;
    • Dheedene, Annelies
    Publication type:
    Article
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    Clinical and molecular spectrum of CHOPS syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2019, v. 179, n. 7, p. 1126, doi. 10.1002/ajmg.a.61174
    By:
    • Raible, Sarah E.;
    • Mehta, Devanshi;
    • Bettale, Chiara;
    • Fiordaliso, Sarah;
    • Kaur, Maninder;
    • Medne, Livija;
    • Rio, Marlene;
    • Haan, Eric;
    • White, Susan M.;
    • Cusmano‐Ozog, Kristina;
    • Nishi, Eriko;
    • Guo, Yiran;
    • Wu, Honglin;
    • Shi, Xiaoqing;
    • Zhao, Qingjie;
    • Zhang, Xueqin;
    • Lei, Qi;
    • Lu, Aimei;
    • He, Xiyu;
    • Okamoto, Nobuhiko
    Publication type:
    Article
    43

    Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disability.

    Published in:
    Brain: A Journal of Neurology, 2020, v. 143, n. 1, p. 112, doi. 10.1093/brain/awz374
    By:
    • Bergen, Nicole J Van;
    • Guo, Yiran;
    • Al-Deri, Noraldin;
    • Lipatova, Zhanna;
    • Stanga, Daniela;
    • Zhao, Sarah;
    • Murtazina, Rakhilya;
    • Gyurkovska, Valeriya;
    • Pehlivan, Davut;
    • Mitani, Tadahiro;
    • Gezdirici, Alper;
    • Antony, Jayne;
    • Collins, Felicity;
    • Willis, Mary J H;
    • Akdemir, Zeynep H Coban;
    • Liu, Pengfei;
    • Punetha, Jaya;
    • Hunter, Jill V;
    • Jhangiani, Shalini N;
    • Fatih, Jawid M
    Publication type:
    Article
    44

    Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disability.

    Published in:
    2019
    By:
    • Van Bergen, Nicole J;
    • Guo, Yiran;
    • Al-Deri, Noraldin;
    • Lipatova, Zhanna;
    • Stanga, Daniela;
    • Zhao, Sarah;
    • Murtazina, Rakhilya;
    • Gyurkovska, Valeriya;
    • Pehlivan, Davut;
    • Mitani, Tadahiro;
    • Gezdirici, Alper;
    • Antony, Jayne;
    • Collins, Felicity;
    • Willis, Mary J H;
    • Coban Akdemir, Zeynep H;
    • Liu, Pengfei;
    • Punetha, Jaya;
    • Hunter, Jill V;
    • Jhangiani, Shalini N;
    • Fatih, Jawid M
    Publication type:
    journal article
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    Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.

    Published in:
    Nature Medicine, 2015, v. 21, n. 9, p. 1018, doi. 10.1038/nm.3933
    By:
    • Li, Yun R;
    • Li, Jin;
    • Zhao, Sihai D;
    • Bradfield, Jonathan P;
    • Mentch, Frank D;
    • Maggadottir, S Melkorka;
    • Hou, Cuiping;
    • Abrams, Debra J;
    • Chang, Diana;
    • Gao, Feng;
    • Guo, Yiran;
    • Wei, Zhi;
    • Connolly, John J;
    • Cardinale, Christopher J;
    • Bakay, Marina;
    • Glessner, Joseph T;
    • Li, Dong;
    • Kao, Charlly;
    • Thomas, Kelly A;
    • Qiu, Haijun
    Publication type:
    Article
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