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Mineralocorticoid Receptor Phosphorylation Regulates Ligand Binding and Renal Response to Volume Depletion and Hyperkalemia

Cell metabolism, 2013-11, Vol.18 (5), p.660-671

2013

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Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4

Proceedings of the National Academy of Sciences - PNAS, 2013-05, Vol.110 (19), p.7838-7843

2013

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Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas

Nature genetics, 2015-09, Vol.47 (9), p.996-1002

2015

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Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

Nature genetics, 2014-10, Vol.46 (10), p.1135-1139

2014

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Calcineurin dephosphorylates Kelch-like 3, reversing phosphorylation by angiotensin II and regulating renal electrolyte handling

Proceedings of the National Academy of Sciences - PNAS, 2019-02, Vol.116 (8), p.3155-3160

2019

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

American journal of human genetics, 2016-08, Vol.99 (2), p.337-351

2016

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Early and multiple origins of metastatic lineages within primary tumors

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (8), p.2140-2145

2016

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K⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

Science (American Association for the Advancement of Science), 2011-02, Vol.331 (6018), p.768-772

2011

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Predictors of Chemosensitivity in Triple Negative Breast Cancer: An Integrated Genomic Analysis

PLoS medicine, 2016-12, Vol.13 (12), p.e1002193-e1002193

2016

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Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Human molecular genetics, 2015-04, Vol.24 (8), p.2318-2329

2015

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Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (45), p.19096-19101

2009

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Isolated polycystic liver disease genes define effectors of polycystin-1 function

The Journal of clinical investigation, 2017-05, Vol.127 (5), p.1772-1785

2017

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KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1)

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (32), p.11864-11869

2014

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Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases

Biochimica et biophysica acta, 2010-12, Vol.1802 (12), p.1150-1158

2010

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Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma

The Journal of clinical investigation, 2016-01, Vol.126 (1), p.169-180

2016

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Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

Nature genetics, 2014-06, Vol.46 (6), p.613-617

2014

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Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (7), p.2915-2920

2011

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Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

Proceedings of the National Academy of Sciences - PNAS, 2009-04, Vol.106 (14), p.5842-5847

2009

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Pioneering a Global Cure for Chronic Hepatitis C Virus Infection

Cell, 2016-09, Vol.167 (1), p.12-15

2016

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Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival

Science signaling, 2019-10, Vol.12 (603)

2019

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The Congenital Heart Disease Genetic Network Study: Cohort description

PloS one, 2018-01, Vol.13 (1), p.e0191319

2018

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Genomic characterization of sarcomatoid transformation in clear cell renal cell carcinoma

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (8), p.2170-2175

2016

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De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis

Proceedings of the National Academy of Sciences - PNAS, 2017-08, Vol.114 (35), p.E7341-E7347

2017

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Molecular physiology of the WNK kinases

Annual review of physiology, 2008-01, Vol.70 (1), p.329-355

2008

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Mineralocorticoid Receptor Phosphorylation Regulates Ligand Binding and Renal Response to Volume Depletion and Hyperkalemia

Kelch-like 3 and Cullin 3 regulate electrolyte homeostasis via ubiquitination and degradation of WNK4

Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation

Calcineurin dephosphorylates Kelch-like 3, reversing phosphorylation by angiotensin II and regulating renal electrolyte handling

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Early and multiple origins of metastatic lineages within primary tumors

K⁺ Channel Mutations in Adrenal Aldosterone-Producing Adenomas and Hereditary Hypertension

Predictors of Chemosensitivity in Triple Negative Breast Cancer: An Integrated Genomic Analysis

Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing

Isolated polycystic liver disease genes define effectors of polycystin-1 function

KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1)

Phosphoregulation of the Na–K–2Cl and K–Cl cotransporters by the WNK kinases

Genetic landscape of metastatic and recurrent head and neck squamous cell carcinoma

Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

Pioneering a Global Cure for Chronic Hepatitis C Virus Infection

Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival

The Congenital Heart Disease Genetic Network Study: Cohort description

Genomic characterization of sarcomatoid transformation in clear cell renal cell carcinoma

De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Molecular physiology of the WNK kinases

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