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Author Details

Moneeza K Siddiqui
University of Dundee, Ninewells Hospital and Medical School
2016
43
12
PMIDPaper TitleJournal TitlePublished Year
36356117Genetic testing for familial hypercholesterolaemia: utility beyond diagnosis.Eur J Prev Cardiol2024
37450899Addressing Ancestry and Sex Bias in Pharmacogenomics.Annu Rev Pharmacol Toxicol2024
36377890Incidence and Outcomes of Patients Receiving Chronic Kidney Replacement Therapy Admitted to Scottish ICUs Between 2009 and 2019-A National Observational Cohort Study.Crit Care Med2023
37563596Competing risks analysis for neutrophil to lymphocyte ratio as a predictor of diabetic retinopathy incidence in the Scottish population.BMC Med2023
37253618A gene risk score using missense variants in SLCO1B1 is associated with earlier onset statin intolerance.Eur Heart J Cardiovasc Pharmacother2023
37308106Common and Distinct Genetic Architecture of Age at Diagnosis of Diabetes in South Indian and European Populations.Diabetes Care2023
36998609The cholesterol-lowering effect of statins is modified by <i>LILRB5</i> intolerance genotype: Results from a recruit-by-genotype clinical trial.Front Pharmacol2023
36624453Weight variability and cardiovascular outcomes: a systematic review and meta-analysis.Cardiovasc Diabetol2023
36691956Major cardiovascular events and subsequent risk of kidney failure with replacement therapy: a CKD Prognosis Consortium study.Eur Heart J2023
34562103Diabetes status modifies the long-term effect of lipoprotein-associated phospholipase A2 on major coronary events.Diabetologia2022
35551093Cardiovascular outcomes in patients with chronic kidney disease and COVID-19: a multi-regional data-linkage study.Eur Respir J2022
35349657Response to Comment on Dawed et al. Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas. Diabetes Care 2021;44:2673-2682.Diabetes Care2022
35471599Correction to: Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.Diabetologia2022
36502833How do we collect good-quality data on race and ethnicity and address the trust gap?Lancet2022
36102151Identification of 4 New Loci Associated With Primary Hyperparathyroidism (PHPT) and a Polygenic Risk Score for PHPT.J Clin Endocrinol Metab2022
36288800Using Data to Improve the Management of Diabetes: The Tayside Experience.Diabetes Care2022
35247066Young-onset diabetes in Asian Indians is associated with lower measured and genetically determined beta cell function.Diabetologia2022
35330732Editorial: Pharmacogenomics of Adverse Drug Reactions.Front Genet2022
35338048Metabolic dysfunction-related liver disease as a risk factor for cancer.BMJ Open Gastroenterol2022
34609928Prescribing Patterns and Response to Antihyperglycemic Agents Among Novel Clusters of Type 2 Diabetes in Asian Indians.Diabetes Technol Ther2022
32948670The Relationship between AKI and CKD in Patients with Type 2 Diabetes: An Observational Cohort Study.J Am Soc Nephrol2021
34950598Evidence of a Causal Relationship between Serum Thyroid-Stimulating Hormone and Osteoporotic Bone Fractures.Eur Thyroid J2021
34583929Performance of prediction models for nephropathy in people with type 2 diabetes: systematic review and external validation study.BMJ2021
34607834Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas.Diabetes Care2021
34659336Common Statin Intolerance Variants in <i>ABCB1</i> and <i>LILRB5</i> Show Synergistic Effects on Statin Response: An Observational Study Using Electronic Health Records.Front Genet2021
34249083Polymorphism in <i>INSR</i> Locus Modifies Risk of Atrial Fibrillation in Patients on Thyroid Hormone Replacement Therapy.Front Genet2021
34172468The association between SARS-CoV-2 RT-PCR cycle threshold and mortality in a community cohort.Eur Respir J2021
34194474The Genetics of Adverse Drug Outcomes in Type 2 Diabetes: A Systematic Review.Front Genet2021
32407295Elevated circulating amyloid concentrations in obesity and diabetes promote vascular dysfunction.J Clin Invest2020
32080354Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment.Pharmacogenomics J2020
32855438Revised 15-item MDS-specific frailty scale maintains prognostic potential.Leukemia2020
32675210Characteristics and outcomes of health and social care workers testing positive for SARS-CoV-2 in the Tayside region of Scotland.Eur Respir J2020
32816869Novel subgroups of type 2 diabetes and their association with microvascular outcomes in an Asian Indian population: a data-driven cluster analysis: the INSPIRED study.BMJ Open Diabetes Res Care2020
32496628Exome Sequencing Reveals Common and Rare Variants in F5 Associated With ACE Inhibitor and Angiotensin Receptor Blocker-Induced Angioedema.Clin Pharmacol Ther2020
31242253Pharmacogenomics of statin-related myopathy: Meta-analysis of rare variants from whole-exome sequencing.PLoS One2019
29623345Lp-PLA<sub>2</sub> activity is associated with increased risk of diabetic retinopathy: a longitudinal disease progression study.Diabetologia2018
30487499Association of Prolonged QTc Dispersion with Diastolic Dysfunction of the Left Ventricle in Patients with Non ST Segment Elevation Myocardial Infarction.Mymensingh Med J2018
28030426Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors.Pharmacogenet Genomics2017
29020356A common missense variant of LILRB5 is associated with statin intolerance and myalgia.Eur Heart J2017
28727628Replication confirms the association of loci in FOXE1, PDE8B, CAPZB and PDE10A with thyroid traits: a Genetics of Diabetes Audit and Research Tayside study (GoDARTS).Pharmacogenet Genomics2017
28790154<i>CKM</i> Glu83Gly Is Associated With Blunted Creatine Kinase Variation, but Not With Myalgia.Circ Cardiovasc Genet2017
26169577A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.Pharmacogenomics J2016
26568611Common Creatine Kinase gene mutation results in falsely reassuring CK levels in muscle disorders.QJM2016
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Collaborators

Colin N A Palmer
Pat Macpherson Centre for Pharmacogenomics and Pharmacogenetics, University of Dundee
Co-authored papers 23
Alex S F Doney
University of Dundee. Ninewells Hospital
Co-authored papers 13
Samira Bell
University of Dundee
Co-authored papers 9
Abirami Veluchamy
Ninewells Hospital and Medical School, University of Dundee
Co-authored papers 8
Viswanathan Mohan
Co-authored papers 6
Anke H Maitland-van der Zee
Amsterdam UMC location University of Amsterdam
Co-authored papers 6
Andrew D Morris
University of Edinburgh
Co-authored papers 4
Patrik K E Magnusson
Co-authored papers 3
Venkatesan Radha
Co-authored papers 3
Daniel I Chasman
Harvard Medical School, Harvard University
Co-authored papers 3
Seyed Hamidreza Mahmoudpour
Institute for Medical Biostatistics, University Medical Center Mainz
Co-authored papers 3
Varinderpal Kaur
Co-authored papers 2
John S Witte
Stanford University School of Medicine
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Ann-Christine Syvänen
Co-authored papers 2
Josep M Mercader
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Sook Wah Yee
University of California San Francisco
Co-authored papers 2
Naveed Sattar
Co-authored papers 2
Monique M Hedderson
Co-authored papers 2
Yoichiro Kamatani
Co-authored papers 2
Josephine H Li
Co-authored papers 2
Yu-Chuan Chang
Chang Gung Memorial Hospital-Linko, Chang Gung University
Co-authored papers 2
Paul M Ridker
Co-authored papers 2
Michiaki Kubo
Co-authored papers 2
Kathleen M Giacomini
University of California San Francisco
Co-authored papers 2
Kenneth M Borthwick
Hood Center for Health Research
Co-authored papers 1
Josef Coresh
Co-authored papers 1
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 1
Morgan E Grams
New York University Grossman School of Medicine
Co-authored papers 1
David S Carrell
Kaiser Permanente Washington Health Research Institute
Co-authored papers 1
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