Works by Crawford, Joanna


Results: 34
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    Social inhibition and treatment-resistant depression.

    Published in:
    Personality & Mental Health, 2007, v. 1, n. 1, p. 62, doi. 10.1002/pmh.5
    By:
    • Crawford, Joanna G.;
    • Parker, Gordon B.;
    • Malhi, Gin S.;
    • Mitchell, Philip B.;
    • Wilhelm, Kay;
    • Proudfoot, Judy
    Publication type:
    Article
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    Genotype-free demultiplexing of pooled single-cell RNA-seq.

    Published in:
    Genome Biology, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s13059-019-1852-7
    By:
    • Xu, Jun;
    • Falconer, Caitlin;
    • Nguyen, Quan;
    • Crawford, Joanna;
    • McKinnon, Brett D.;
    • Mortlock, Sally;
    • Senabouth, Anne;
    • Andersen, Stacey;
    • Chiu, Han Sheng;
    • Jiang, Longda;
    • Palpant, Nathan J.;
    • Yang, Jian;
    • Mueller, Michael D.;
    • Hewitt, Alex W.;
    • Pébay, Alice;
    • Montgomery, Grant W.;
    • Powell, Joseph E.;
    • Coin, Lachlan J.M
    Publication type:
    Article
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    Corrigendum: Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 3, p. 304, doi. 10.1038/ng0315-304b
    By:
    • Simons, Cas;
    • Rash, Lachlan D;
    • Crawford, Joanna;
    • Ma, Linlin;
    • Cristofori-Armstrong, Ben;
    • Miller, David;
    • Ru, Kelin;
    • Baillie, Gregory J;
    • Alanay, Yasemin;
    • Jacquinet, Adeline;
    • Debray, François-Guillaume;
    • Verloes, Alain;
    • Shen, Joseph;
    • Yesil, Gözde;
    • Guler, Serhat;
    • Yuksel, Adnan;
    • Cleary, John G;
    • Grimmond, Sean M;
    • McGaughran, Julie;
    • King, Glenn F
    Publication type:
    Article
    12

    Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsy.

    Published in:
    Nature Genetics, 2015, v. 47, n. 1, p. 73, doi. 10.1038/ng.3153
    By:
    • Simons, Cas;
    • Rash, Lachlan D;
    • Crawford, Joanna;
    • Ma, Linlin;
    • Cristofori-Armstrong, Ben;
    • Ru, Kelin;
    • Baillie, Gregory J;
    • King, Glenn F;
    • McGaughran, Julie;
    • Gabbett, Michael T;
    • Taft, Ryan J;
    • Miller, David;
    • Alanay, Yasemin;
    • Jacquinet, Adeline;
    • Debray, François-Guillaume;
    • Verloes, Alain;
    • Shen, Joseph;
    • Yesil, Gözde;
    • Guler, Serhat;
    • Yuksel, Adnan
    Publication type:
    Article
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    Spatial transcriptomic analysis of Sonic hedgehog medulloblastoma identifies that the loss of heterogeneity and promotion of differentiation underlies the response to CDK4/6 inhibition.

    Published in:
    Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01185-4
    By:
    • Vo, Tuan;
    • Balderson, Brad;
    • Jones, Kahli;
    • Ni, Guiyan;
    • Crawford, Joanna;
    • Millar, Amanda;
    • Tolson, Elissa;
    • Singleton, Matthew;
    • Kojic, Marija;
    • Robertson, Thomas;
    • Walters, Shaun;
    • Mulay, Onkar;
    • Bhuva, Dharmesh D.;
    • Davis, Melissa J.;
    • Wainwright, Brandon J.;
    • Nguyen, Quan;
    • Genovesi, Laura A.
    Publication type:
    Article
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    X-linked hypomyelination with spondylometaphyseal dysplasia (H-SMD) associated with mutations in AIFM1.

    Published in:
    Neurogenetics, 2017, v. 18, n. 4, p. 185, doi. 10.1007/s10048-017-0520-x
    By:
    • Miyake, Noriko;
    • Wolf, Nicole;
    • Cayami, Ferdy;
    • Crawford, Joanna;
    • Bley, Annette;
    • Bulas, Dorothy;
    • Conant, Alex;
    • Bent, Stephen;
    • Gripp, Karen;
    • Hahn, Andreas;
    • Humphray, Sean;
    • Kimura-Ohba, Shihoko;
    • Kingsbury, Zoya;
    • Lajoie, Bryan;
    • Lal, Dennis;
    • Micha, Dimitra;
    • Pizzino, Amy;
    • Sinke, Richard;
    • Sival, Deborah;
    • Stolte-Dijkstra, Irene
    Publication type:
    Article
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    Biallelic PI4KA variants cause neurological, intestinal and immunological disease.

    Published in:
    2021
    By:
    • Salter, Claire G;
    • Cai, Yiying;
    • Lo, Bernice;
    • Helman, Guy;
    • Taylor, Henry;
    • McCartney, Amber;
    • Leslie, Joseph S;
    • Accogli, Andrea;
    • Zara, Federico;
    • Traverso, Monica;
    • Fasham, James;
    • Lees, Joshua A;
    • Ferla, Matteo P;
    • Chioza, Barry A;
    • Wenger, Olivia;
    • Scott, Ethan;
    • Cross, Harold E;
    • Crawford, Joanna;
    • Warshawsky, Ilka;
    • Keisling, Matthew
    Publication type:
    journal article
    26

    A recurrent de novo mutation in TMEM106B causes hypomyelinating leukodystrophy.

    Published in:
    2017
    By:
    • Simons, Cas;
    • Dyment, David;
    • Bent, Stephen J.;
    • Crawford, Joanna;
    • D'Hooghe, Marc;
    • Kohlschütter, Alfried;
    • Venkateswaran, Sunita;
    • Helman, Guy;
    • Poll-The, Bwee-Tien;
    • Makowski, Christine C.;
    • Yoko Ito;
    • Kernohan, Kristin;
    • Hartley, Taila;
    • Waisfisz, Quinten;
    • Taft, Ryan J.;
    • van der Knaap, Marjo S.;
    • Wolf, Nicole I.;
    • Ito, Yoko;
    • Care4Rare Consortium
    Publication type:
    journal article
    27

    Whole exome sequencing in patients with white matter abnormalities.

    Published in:
    2016
    By:
    • Vanderver, Adeline;
    • Simons, Cas;
    • Helman, Guy;
    • Crawford, Joanna;
    • Wolf, Nicole I.;
    • Bernard, Geneviève;
    • Pizzino, Amy;
    • Schmidt, Johanna L.;
    • Takanohashi, Asako;
    • Miller, David;
    • Khouzam, Amirah;
    • Rajan, Vani;
    • Ramos, Erica;
    • Chowdhury, Shimul;
    • Hambuch, Tina;
    • Ru, Kelin;
    • Baillie, Gregory J.;
    • Grimmond, Sean M.;
    • Caldovic, Ljubica;
    • Devaney, Joseph
    Publication type:
    journal article
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    Quantitative gene profiling of long noncoding RNAs with targeted RNA sequencing.

    Published in:
    Nature Methods, 2015, v. 12, n. 4, p. 339, doi. 10.1038/nmeth.3321
    By:
    • Clark, Michael B;
    • Mercer, Tim R;
    • Bussotti, Giovanni;
    • Leonardi, Tommaso;
    • Haynes, Katelin R;
    • Crawford, Joanna;
    • Brunck, Marion E;
    • Cao, Kim-Anh Lê;
    • Thomas, Gethin P;
    • Chen, Wendy Y;
    • Taft, Ryan J;
    • Nielsen, Lars K;
    • Enright, Anton J;
    • Mattick, John S;
    • Dinger, Marcel E
    Publication type:
    Article
    29

    Genome sequencing in persistently unsolved white matter disorders.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 144, doi. 10.1002/acn3.50957
    By:
    • Helman, Guy;
    • Lajoie, Bryan R.;
    • Crawford, Joanna;
    • Takanohashi, Asako;
    • Walkiewicz, Marzena;
    • Dolzhenko, Egor;
    • Gross, Andrew M.;
    • Gainullin, Vladimir G.;
    • Bent, Stephen J.;
    • Jenkinson, Emma M.;
    • Ferdinandusse, Sacha;
    • Waterham, Hans R.;
    • Dorboz, Imen;
    • Bertini, Enrico;
    • Miyake, Noriko;
    • Wolf, Nicole I.;
    • Abbink, Truus E. M.;
    • Kirwin, Susan M.;
    • Tan, Christina M.;
    • Hobson, Grace M.
    Publication type:
    Article
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    Expression and Function of the Protein Tyrosine Phosphatase Receptor J (PTPRJ) in Normal Mammary Epithelial Cells and Breast Tumors.

    Published in:
    PLoS ONE, 2012, v. 7, n. 7, p. 1, doi. 10.1371/journal.pone.0040742
    By:
    • Smart, Chanel E.;
    • Amiri, Marjan E. Askarian;
    • Wronski, Ania;
    • Dinger, Marcel E.;
    • Crawford, Joanna;
    • Ovchinnikov, Dmitry A.;
    • Vargas, Ana Cristina;
    • Reid, Lynne;
    • Simpson, Peter T.;
    • Song, Sarah;
    • Wiesner, Christiane;
    • French, Juliet D.;
    • Dave, Richa K.;
    • Silva, Leonard da;
    • Purdon, Amy;
    • Andrew, Megan;
    • Mattick, John S.;
    • Lakhani, Sunil R.;
    • Brown, Melissa A.;
    • Kellie, Stuart
    Publication type:
    Article
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    The Evx1/Evx1as gene locus regulates anterior-posterior patterning during gastrulation.

    Published in:
    Scientific Reports, 2016, p. 26657, doi. 10.1038/srep26657
    By:
    • Bell, Charles C.;
    • Amaral, Paulo P.;
    • Kalsbeek, Anton;
    • Magor, Graham W.;
    • Gillinder, Kevin R.;
    • Tangermann, Pierre;
    • di Lisio, Lorena;
    • Cheetham, Seth W.;
    • Gruhl, Franziska;
    • Frith, Jessica;
    • Tallack, Michael R.;
    • Ru, Ke-Lin;
    • Crawford, Joanna;
    • Mattick, John S.;
    • Dinger, Marcel E.;
    • Perkins, Andrew C.
    Publication type:
    Article
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