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IJCM_277A: Awareness, Perception and Attitude of Medical Interns and Graduates Towards Robotic Surgery: A Cross-Sectional Study

Indian journal of community medicine, 2024-04, Vol.49 (Suppl 1), p.S80-S80

2024

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IJCM_228A: Awareness & possession of health insurance scheme and its impact on health care utilization amongst people seeking services in tertiary care hospitals of coastal Karnataka: A cross-sectional study

Indian journal of community medicine, 2024-04, Vol.49 (Suppl 1), p.S66-S66

2024

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Hesitancy towards Japanese Encephalitis vaccine and its socio-demographic correlates among parents attending to children aged <15 years in tertiary hospitals of Coastal South India

Clinical epidemiology and global health, 2024-05, Vol.27, p.101585, Article 101585

2024

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Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency

PLoS genetics, 2013-02, Vol.9 (2), p.e1003301

2013

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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Journal of the American College of Cardiology, 2004-11, Vol.44 (9), p.1903-1910

2004

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Echocardiography-guided genetic testing in hypertrophic cardiomyopathy : Septal morphological features predict the presence of myofilament mutations

Mayo Clinic proceedings, 2006-04, Vol.81 (4), p.459-467

2006

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Sarcomeric Genotyping in Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2005-04, Vol.80 (4), p.463-469

2005

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Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2003-07, Vol.108 (4), p.445-451

2003

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Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

Nature genetics, 2003-12, Vol.35 (4), p.315-317

2003

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Enhancing Reuse of Data and Biological Material in Medical Research: From FAIR to FAIR-Health

Biopreservation and biobanking, 2018-04, Vol.16 (2), p.97

2018

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Whole-genome sequence variation, population structure and demographic history of the Dutch population

Nature genetics, 2014-08, Vol.46 (8), p.818-825

2014

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Yield of genetic testing in hypertrophic cardiomyopathy

Mayo Clinic proceedings, 2005-06, Vol.80 (6), p.739-744

2005

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American Society of Hematology 2018 Guidelines for management of venous thromboembolism: treatment of pediatric venous thromboembolism

Blood advances, 2018-11, Vol.2 (22), p.3292-3316

2018

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Comprehensive Analysis of the Beta-Myosin Heavy Chain Gene in 389 Unrelated Patients With Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2004-08, Vol.44 (3), p.602-610

2004

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Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

Journal of the American College of Cardiology, 2002-06, Vol.39 (12), p.2042-2048

2002

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Gating and intrafraction drift correction on a 1.5 T MR-Linac: Clinical dosimetric benefits for upper abdominal tumors

Radiotherapy and oncology, 2023-12, Vol.189, p.109932-109932, Article 109932

2023

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Gene-specific modifying effects of pro-LVH polymorphisms involving the renin–angiotensin–aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy

European heart journal, 2005-11, Vol.26 (22), p.2457-2462

2005

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Prevalence and severity of benign mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2002-12, Vol.106 (24), p.3085-3090

2002

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Population-specific genotype imputations using minimac or IMPUTE2

Nature protocols, 2015-09, Vol.10 (9), p.1285-1296

2015

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Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'

European journal of human genetics : EJHG, 2014-11, Vol.22 (11), p.1321-1326

2014

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A Case for Inclusion of Genetic Counselors in Cardiac Care

Cardiology in review, 2016-03, Vol.24 (2), p.49-55

2016

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WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

Scientific reports, 2019-12, Vol.9 (1), p.18758, Article 18758

2019

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A framework for the detection of de novo mutations in family-based sequencing data

European journal of human genetics : EJHG, 2017-02, Vol.25 (2), p.227-233

2017

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Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy

Molecular genetics and metabolism, 2005-08, Vol.85 (4), p.280-285

2005

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Yield of Genetic Testing in Hypertrophic Cardiomyopathy

Mayo Clinic proceedings, 2005-06, Vol.80 (6), p.739-744

2005

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IJCM_277A: Awareness, Perception and Attitude of Medical Interns and Graduates Towards Robotic Surgery: A Cross-Sectional Study

IJCM_228A: Awareness & possession of health insurance scheme and its impact on health care utilization amongst people seeking services in tertiary care hospitals of coastal Karnataka: A cross-sectional study

Hesitancy towards Japanese Encephalitis vaccine and its socio-demographic correlates among parents attending to children aged <15 years in tertiary hospitals of Coastal South India

Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Echocardiography-guided genetic testing in hypertrophic cardiomyopathy : Septal morphological features predict the presence of myofilament mutations

Sarcomeric Genotyping in Hypertrophic Cardiomyopathy

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

Enhancing Reuse of Data and Biological Material in Medical Research: From FAIR to FAIR-Health

Whole-genome sequence variation, population structure and demographic history of the Dutch population

Yield of genetic testing in hypertrophic cardiomyopathy

American Society of Hematology 2018 Guidelines for management of venous thromboembolism: treatment of pediatric venous thromboembolism

Comprehensive Analysis of the Beta-Myosin Heavy Chain Gene in 389 Unrelated Patients With Hypertrophic Cardiomyopathy

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective

Gating and intrafraction drift correction on a 1.5 T MR-Linac: Clinical dosimetric benefits for upper abdominal tumors

Gene-specific modifying effects of pro-LVH polymorphisms involving the renin–angiotensin–aldosterone system among 389 unrelated patients with hypertrophic cardiomyopathy

Prevalence and severity of benign mutations in the β-myosin heavy chain, cardiac troponin T, and α-tropomyosin genes in hypertrophic cardiomyopathy

Population-specific genotype imputations using minimac or IMPUTE2

Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'

A Case for Inclusion of Genetic Counselors in Cardiac Care

WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene

A framework for the detection of de novo mutations in family-based sequencing data

Molecular and functional characterization of a human frataxin mutation found in hypertrophic cardiomyopathy

Yield of Genetic Testing in Hypertrophic Cardiomyopathy

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