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Determining protein structures using deep mutagenesis

Nature genetics, 2019-07, Vol.51 (7), p.1177-1186

2019

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Comprehensive characterization of protein-protein interactions perturbed by disease mutations

Nature genetics, 2021-03, Vol.53 (3), p.342-353

2021

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Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

Nature genetics, 2016-01, Vol.48 (1), p.67-73

2016

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Senescence bypass screen identifies TBX2 , which represses Cdkn2a ( p19 ARF ) and is amplified in a subset of human breast cancers

Nature genetics, 2000-11, Vol.26 (3), p.291-299

2000

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Inferring protein 3D structure from deep mutation scans

Nature genetics, 2019-07, Vol.51 (7), p.1170-1176

2019

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BMP signaling controls muscle mass

Nature genetics, 2013-11, Vol.45 (11), p.1309-1318

2013

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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Nature genetics, 2015-08, Vol.47 (8), p.926-932

2015

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Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Nature genetics, 2021-03, Vol.53 (3), p.294-303

2021

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Activation of the AXL kinase causes resistance to EGFR-targeted therapy in lung cancer

Nature genetics, 2012-08, Vol.44 (8), p.852-860

2012

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Identification of H3K4me1-associated proteins at mammalian enhancers

Nature genetics, 2018-01, Vol.50 (1), p.73-82

2018

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Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells

Nature genetics, 2008-07, Vol.40 (7), p.871-879

2008

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Analysis of yeast protein kinases using protein chips

Nature genetics, 2000-11, Vol.26 (3), p.283-289

2000

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SWI/SNF complex in cancer

Nature genetics, 2017-02, Vol.49 (2), p.178-179

2017

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t(11;19)(q21;p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway

Nature genetics, 2003-02, Vol.33 (2), p.208-213

2003

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AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1

Nature genetics, 2000-03, Vol.24 (3), p.245-250

2000

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Proteins shaping global chromatin accessibility

Nature genetics, 2024-03, Vol.56 (3), p.367-368

2024

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Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer's disease pathogenesis

Nature genetics, 2021-02, Vol.53 (2), p.143-146

2021

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Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism

Nature genetics, 2009-02, Vol.41 (2), p.234-239

2009

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Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes

Nature genetics, 2015, Vol.47 (1), p.13-21

2015

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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Nature genetics, 2016-09, Vol.48 (9), p.1043-1048

2016

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Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

Nature genetics, 2008-11, Vol.40 (11), p.1348-1353

2008

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Heterotrimeric G proteins regulate nitrogen-use efficiency in rice

Nature genetics, 2014-06, Vol.46 (6), p.652-656

2014

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Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Nature genetics, 2017-10, Vol.49 (10), p.1529-1538

2017

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Determining protein structures using deep mutagenesis

Comprehensive characterization of protein-protein interactions perturbed by disease mutations

Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease

Senescence bypass screen identifies TBX2 , which represses Cdkn2a ( p19 ARF ) and is amplified in a subset of human breast cancers

Inferring protein 3D structure from deep mutation scans

BMP signaling controls muscle mass

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

Activation of the AXL kinase causes resistance to EGFR-targeted therapy in lung cancer

Identification of H3K4me1-associated proteins at mammalian enhancers

Dishevelled controls apical docking and planar polarization of basal bodies in ciliated epithelial cells

Analysis of yeast protein kinases using protein chips

SWI/SNF complex in cancer

t(11;19)(q21;p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway

AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1

Proteins shaping global chromatin accessibility

Integrating human brain proteomes with genome-wide association data implicates new proteins in Alzheimer's disease pathogenesis

LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression

Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism

Spectrum of diverse genomic alterations define non-clear cell renal carcinoma subtypes

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

Heterotrimeric G proteins regulate nitrogen-use efficiency in rice

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

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