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Annals of Hematology, ISSN 0939-5555, 1/2019, Volume 98, Issue 1, pp. 215 - 218
...LETTER TO THE EDITOR Risk of viral reactivation in patients with occult hepatitis B virus infection during ruxolitinib treatment Harinder Gill 1 & Garret M. K... 
Medicine & Public Health | Hematology | Oncology | PATHOGENESIS | LYMPHOMA | STEM-CELL TRANSPLANTATION | HEMATOLOGY
Journal Article
British journal of haematology, ISSN 0007-1048, 2017, Volume 176, Issue 6, pp. 991 - 994
Journal Article
Journal Article
by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature (London), ISSN 1476-4687, 2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 04/2012, Volume 20, Issue 4, pp. 381 - 388
Journal Article
British Journal of Haematology, ISSN 0007-1048, 08/2017, Volume 178, Issue 3, pp. 349 - 349
Journal Article
Advances in hematology, ISSN 1687-9112, 2010, Volume 2010, pp. 1 - 5
The World Health Organization (WHO) classification recognizes 2 main categories of natural killer (NK) cell-derived neoplasms, namely, extranodal NK/T-cell... 
Review
Journal Article
Annals of hematology, ISSN 1432-0584, 2018, Volume 98, Issue 4, pp. 869 - 879
... with myelofibrosis Harinder Gill 1 & Ho-Wan Ip 2 & Rita Yim 1 & Wing-Fai Tang 2 & Herbert H. Pang 3 & Paul Lee 1 & Garret M. K. Leung 1 & Jamilla Li 1 & Karen Tang 1 & Jason C... 
Secondary | Myelofibrosis | Next-generation sequencing | Prognosis | Medicine & Public Health | Hematology | Primary | Oncology | SYSTEM | MPL | MODEL | ESSENTIAL THROMBOCYTHEMIA | INTERNATIONAL WORKING GROUP | CLINICAL-RELEVANCE | POST-POLYCYTHEMIA-VERA | CALR | JAK2 | HEMATOLOGY | PREDICT SURVIVAL | Gene mutations | Analysis | Genes | Leukemia | Genetic research | Hemoglobin | Genetic aspects | Tumor proteins | Mutation | Gender | Medical prognosis
Journal Article
Schizophrenia Bulletin, ISSN 0586-7614, 04/2019, Volume 45, Issue Supplement_2, pp. S271 - S272
Abstract Background The risk of impulsive aggression is elevated in schizophrenia and reducing the risk of violent acts in patients is a critical to their... 
Poster Session II
Journal Article
Schizophrenia Bulletin, ISSN 0586-7614, 04/2019, Volume 45, Issue Supplement_2, pp. S217 - S218
Abstract Background The association between schizophrenia and violence is an important issue in psychiatry. The impact of several factors (social cognition,... 
Poster Session I
Journal Article
Annals of Hematology, ISSN 0939-5555, 6/2015, Volume 94, Issue 6, pp. 1049 - 1051
...LETTER TO THE EDITOR FLT3 internal tandem duplication in acute promyelocytic leukemia: central nervous system relapse Harinder Gill & Ho-Wan Ip & Annie W. K... 
Medicine & Public Health | Hematology | Oncology | HEMATOLOGY | fms-Like Tyrosine Kinase 3 - genetics | Recurrence | Base Sequence | Humans | Middle Aged | Molecular Sequence Data | Leukemia, Promyelocytic, Acute - diagnosis | Male | Leukemia, Promyelocytic, Acute - genetics | Tandem Repeat Sequences - genetics | Relapse | Diseases
Journal Article
Human mutation, ISSN 1059-7794, 2012, Volume 33, Issue 8, pp. 1261 - 1266