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Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Nature (London), 2016-06, Vol.534 (7605), p.47-54

2016

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Mutational landscape and significance across 12 major cancer types

Nature (London), 2013-10, Vol.502 (7471), p.333-339

2013

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GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers

Genome biology, 2011-04, Vol.12 (4), p.R41-R41, Article R41

2011

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SWI/SNF-mutant cancers depend on catalytic and non-catalytic activity of EZH2

Nature medicine, 2015-12, Vol.21 (12), p.1491-1496

2015

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The mTOR signalling cascade: paving new roads to cure neurological disease

Nature reviews. Neurology, 2016-07, Vol.12 (7), p.379-392

Crino, Peter B.

2016

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The nuclear pore complex: understanding its function through structural insight

Nature reviews. Molecular cell biology, 2017-02, Vol.18 (2), p.73-89

2017

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Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins

Nature medicine, 2016-06, Vol.22 (6), p.672-678

2016

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RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Leukemia, 2016-11, Vol.30 (11), p.2160-2168

2016

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Identification of recurrent SMO and BRAF mutations in ameloblastomas

Nature genetics, 2014-07, Vol.46 (7), p.722-725

2014

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Genetics of amyotrophic lateral sclerosis: an update

Molecular neurodegeneration, 2013-08, Vol.8 (1), p.28-28, Article 28

2013

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The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia

Leukemia, 2017-10, Vol.31 (10), p.2211-2218

2017

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Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-289, Article 289

2020

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Donor cell leukemia arising from preleukemic clones with a novel germline DDX41 mutation after allogenic hematopoietic stem cell transplantation

Leukemia, 2017-04, Vol.31 (4), p.1020-1022

2017

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Progress in mitochondrial replacement therapies

Nature reviews. Molecular cell biology, 2018-02, Vol.19 (2), p.71-72

2018

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Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

Genome Biology, 2011-10, Vol.12 (10), p.R103-R103

2011

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Comprehensive integrative profiling of upper tract urothelial carcinomas

Genome Biology, 2021-01, Vol.22 (1), p.7-7, Article 7

2021

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Genomic determinants of chronic myelomonocytic leukemia

Leukemia, 2017-12, Vol.31 (12), p.2815-2823

2017

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Prostate Cancer-associated SPOP mutations enhance cancer cell survival and docetaxel resistance by upregulating Caprin1-dependent stress granule assembly

Molecular cancer, 2019-11, Vol.18 (1), p.170-14, Article 170

2019

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Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations

Molecular psychiatry, 2016-07, Vol.21 (7), p.885-893

2016

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Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders

Movement disorders clinical practice (Hoboken, N.J.), 2021-01, Vol.8 (1), p.118-125

2021

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Emergence of Developmental Delay in Infants and Toddlers With an FMR1 Mutation

Pediatrics (Evanston), 2021-05, Vol.147 (5), p.1

2021

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Molecular Surveillance of Antimicrobial Resistance of Mycobacterium leprae from Leprosy Patients in Zhejiang Province, China

Infection and drug resistance, 2022-01, Vol.15, p.4029-4036

2022

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Analysing the Cyanobacterial PipX Interaction Network Using NanoBiT Complementation in ISynechococcus elongatus/I PCC7942

International journal of molecular sciences, 2024-05, Vol.25 (9)

2024

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Oncogenic KRAS blockade therapy: renewed enthusiasm and persistent challenges

Molecular cancer, 2021-10, Vol.20 (1), p.128-128, Article 128

2021

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Landscape of somatic mutations in 560 breast cancer whole-genome sequences

Mutational landscape and significance across 12 major cancer types

GISTIC2.0 facilitates sensitive and confident localization of the targets of focal somatic copy-number alteration in human cancers

SWI/SNF-mutant cancers depend on catalytic and non-catalytic activity of EZH2

The mTOR signalling cascade: paving new roads to cure neurological disease

The nuclear pore complex: understanding its function through structural insight

Modulation of splicing catalysis for therapeutic targeting of leukemia with mutations in genes encoding spliceosomal proteins

RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis

Identification of recurrent SMO and BRAF mutations in ameloblastomas

Genetics of amyotrophic lateral sclerosis: an update

The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia

Clinical features of genetically characterized types of hereditary angioedema with normal C1 inhibitor: a systematic review of qualitative evidence

Donor cell leukemia arising from preleukemic clones with a novel germline DDX41 mutation after allogenic hematopoietic stem cell transplantation

Progress in mitochondrial replacement therapies

Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

Comprehensive integrative profiling of upper tract urothelial carcinomas

Genomic determinants of chronic myelomonocytic leukemia

Prostate Cancer-associated SPOP mutations enhance cancer cell survival and docetaxel resistance by upregulating Caprin1-dependent stress granule assembly

Exome sequencing for bipolar disorder points to roles of de novo loss-of-function and protein-altering mutations

Beyond Typical Ataxia Telangiectasia: How to Identify the Ataxia Telangiectasia‐Like Disorders

Emergence of Developmental Delay in Infants and Toddlers With an FMR1 Mutation

Molecular Surveillance of Antimicrobial Resistance of Mycobacterium leprae from Leprosy Patients in Zhejiang Province, China

Analysing the Cyanobacterial PipX Interaction Network Using NanoBiT Complementation in ISynechococcus elongatus/I PCC7942

Oncogenic KRAS blockade therapy: renewed enthusiasm and persistent challenges

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