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Hierarchical Control of Community Grid for Residential Houses

2018 15th IEEE India Council International Conference (INDICON), 2018, p.1-6

2018

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Simulated Annealing Based Fractional Order PID Controller for a Heavy Duty Gas Turbine Plant

2018 3rd IEEE International Conference on Recent Trends in Electronics, Information & Communication Technology (RTEICT), 2018, p.315-318

2018

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Lupus Anticoagulant and Abnormal Coagulation Tests in Patients with Covid-19

The New England journal of medicine, 2020-07, Vol.383 (3), p.288-290

2020

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Whole-genome sequencing of a sporadic primary immunodeficiency cohort

Nature (London), 2020-07, Vol.583 (7814), p.90-95

2020

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

American journal of human genetics, 2017-01, Vol.100 (1), p.75-90

2017

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Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Nature genetics, 2015-12, Vol.47 (12), p.1415-1425

2015

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Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Nature genetics, 2012-09, Vol.44 (9), p.981-990

2012

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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Nature genetics, 2011-04, Vol.43 (4), p.333-338

2011

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A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Blood, 2016-06, Vol.127 (23), p.2791-2803

2016

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Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2017-11, Vol.136 (21), p.2022-2033

2017

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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

The lancet respiratory medicine, 2019-03, Vol.7 (3), p.227-238

2019

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Large-scale gene-centric analysis identifies novel variants for coronary artery disease

PLoS genetics, 2011-09, Vol.7 (9), p.e1002260-e1002260

2011

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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

Nature communications, 2022-08, Vol.13 (1), p.4840-4840, Article 4840

2022

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Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

International journal of epidemiology, 2016-12, Vol.45 (6), p.1927-1937

2016

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Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

American journal of human genetics, 2018-07, Vol.103 (1), p.3-18

2018

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Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

Scientific reports, 2018-01, Vol.8 (1), p.1300-17, Article 1300

2018

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De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

American journal of human genetics, 2018-07, Vol.103 (1), p.144-153

2018

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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy

Investigative ophthalmology & visual science, 2017-06, Vol.58 (7), p.2906-2914

2017

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Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits

PLoS genetics, 2011-06, Vol.7 (6), p.e1002139-e1002139

2011

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Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

American journal of human genetics, 2011-01, Vol.88 (1), p.6-18

2011

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Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study

Heart (British Cardiac Society), 2010-12, Vol.96 (24), p.1985-1989

2010

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Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

Human molecular genetics, 2013-01, Vol.22 (1), p.184-201

2013

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Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

American journal of human genetics, 2017-02, Vol.100 (2), p.334-342

2017

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Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort

Nature (London), 2020-08, Vol.584 (7819), p.E2-E2

2020

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Hierarchical Control of Community Grid for Residential Houses

Simulated Annealing Based Fractional Order PID Controller for a Heavy Duty Gas Turbine Plant

Lupus Anticoagulant and Abnormal Coagulation Tests in Patients with Covid-19

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

Large-scale gene-centric analysis identifies novel variants for coronary artery disease

GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements

Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis

Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data

De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy

Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits

Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height

Family history of premature coronary heart disease and risk prediction in the EPIC-Norfolk prospective population study

Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals

Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort

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