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A network-biology perspective of microRNA function and dysfunction in cancer

Nature reviews. Genetics, 2016-12, Vol.17 (12), p.719-732

2016

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HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse

PLoS genetics, 2015-10, Vol.11 (10), p.e1005620-e1005620

2015

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Splice factor mutations and alternative splicing as drivers of hematopoietic malignancy

Immunological reviews, 2015-01, Vol.263 (1), p.257-278

2015

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Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway

PLoS genetics, 2012-07, Vol.8 (7), p.e1002772-e1002772

2012

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GATA2 is required for lymphatic vessel valve development and maintenance

The Journal of clinical investigation, 2015-08, Vol.125 (8), p.2979-2994

2015

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Recurrent targeted genes of hepatitis B virus in the liver cancer genomes identified by a next-generation sequencing-based approach

PLoS genetics, 2012-12, Vol.8 (12), p.e1003065-e1003065

2012

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ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation

PLoS genetics, 2013-10, Vol.9 (10), p.e1003895-e1003895

2013

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Comprehensive analysis of transcriptome variation uncovers known and novel driver events in T-cell acute lymphoblastic leukemia

PLoS genetics, 2013-12, Vol.9 (12), p.e1003997

2013

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Germline genetic variants that predispose to myeloproliferative neoplasms and hereditary myeloproliferative phenotypes

Leukemia research, 2024-11, Vol.146, p.107566, Article 107566

2024

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mDia formins form hetero-oligomers and cooperatively maintain murine hematopoiesis

PLoS genetics, 2023-12, Vol.19 (12), p.e1011084-e1011084

2023

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Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

Genetics in medicine, 2022-08, Vol.24 (8), p.1753-1760

2022

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A comparative analysis of algorithms for somatic SNV detection in cancer

Bioinformatics, 2013-09, Vol.29 (18), p.2223-2230

2013

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Myeloid neoplasms with germline DDX41 mutation

International journal of hematology, 2017-08, Vol.106 (2), p.163-174

2017

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Use of within-array replicate spots for assessing differential expression in microarray experiments

Bioinformatics, 2005-05, Vol.21 (9), p.2067-2075

2005

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GATA2 deficiency syndrome: A decade of discovery

Human mutation, 2021-11, Vol.42 (11), p.1399-1421

2021

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Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia

Leukemia, 2020-08, Vol.34 (8), p.2051-2063

2020

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A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal Erythropoiesis

PLoS genetics, 2015-10, Vol.11 (10), p.e1005526-e1005526

2015

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Increased Prevalence of Germline Pathogenic CHEK2 Variants in Individuals With Pituitary Adenomas

The journal of clinical endocrinology and metabolism, 2024-10, Vol.109 (11), p.2720-2728

2024

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Medullary thymic epithelial cells expressing Aire represent a unique lineage derived from cells expressing claudin

Nature Immunology, 2007-03, Vol.8 (3), p.304-311

2007

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Post-Aire maturation of thymic medullary epithelial cells involves selective expression of keratinocyte-specific autoantigens

Frontiers in immunology, 2012-01, Vol.3 (March), p.19-19

2012

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Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice

PLoS genetics, 2017-05, Vol.13 (5), p.e1006716-e1006716

2017

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A network-biology perspective of microRNA function and dysfunction in cancer

HENMT1 and piRNA Stability Are Required for Adult Male Germ Cell Transposon Repression and to Define the Spermatogenic Program in the Mouse

Splice factor mutations and alternative splicing as drivers of hematopoietic malignancy

Loss of ATRX, genome instability, and an altered DNA damage response are hallmarks of the alternative lengthening of telomeres pathway

miR-199a-5p Is upregulated during fibrogenic response to tissue injury and mediates TGFbeta-induced lung fibroblast activation by targeting caveolin-1

GATA2 is required for lymphatic vessel valve development and maintenance

Recurrent targeted genes of hepatitis B virus in the liver cancer genomes identified by a next-generation sequencing-based approach

ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation

Comprehensive analysis of transcriptome variation uncovers known and novel driver events in T-cell acute lymphoblastic leukemia

Germline genetic variants that predispose to myeloproliferative neoplasms and hereditary myeloproliferative phenotypes

mDia formins form hetero-oligomers and cooperatively maintain murine hematopoiesis

Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort

A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome

A comparative analysis of algorithms for somatic SNV detection in cancer

Myeloid neoplasms with germline DDX41 mutation

Use of within-array replicate spots for assessing differential expression in microarray experiments

GATA2 deficiency syndrome: A decade of discovery

Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia

A Systems Approach Identifies Essential FOXO3 Functions at Key Steps of Terminal Erythropoiesis

Increased Prevalence of Germline Pathogenic CHEK2 Variants in Individuals With Pituitary Adenomas

Medullary thymic epithelial cells expressing Aire represent a unique lineage derived from cells expressing claudin

Post-Aire maturation of thymic medullary epithelial cells involves selective expression of keratinocyte-specific autoantigens

Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer

Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice

A Syntenic Cross Species Aneuploidy Genetic Screen Links RCAN1 Expression to β-Cell Mitochondrial Dysfunction in Type 2 Diabetes

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