Dennis O. Mook‐Kanamori

ORCID: 0000-0002-0182-5122
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About
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Research Areas
  • Metabolomics and Mass Spectrometry Studies
  • Genetic Associations and Epidemiology
  • Birth, Development, and Health
  • Diet and metabolism studies
  • Liver Disease Diagnosis and Treatment
  • Adipose Tissue and Metabolism
  • Cardiac electrophysiology and arrhythmias
  • Diabetes, Cardiovascular Risks, and Lipoproteins
  • Bioinformatics and Genomic Networks
  • Epigenetics and DNA Methylation
  • Obesity, Physical Activity, Diet
  • Cardiomyopathy and Myosin Studies
  • Lipoproteins and Cardiovascular Health
  • Diet, Metabolism, and Disease
  • Adipokines, Inflammation, and Metabolic Diseases
  • Nutrition, Genetics, and Disease
  • Gestational Diabetes Research and Management
  • Antioxidant Activity and Oxidative Stress
  • Neonatal Respiratory Health Research
  • Cardiovascular Disease and Adiposity
  • RNA modifications and cancer
  • Lipid metabolism and biosynthesis
  • Nutritional Studies and Diet
  • Cholesterol and Lipid Metabolism
  • Advanced Glycation End Products research

Leiden University
2014-2025

Leiden University Medical Center
2015-2024

Weatherford College
2024

The University of Tokyo
2023

Icahn School of Medicine at Mount Sinai
2023

The Lundquist Institute
2023

Harbor–UCLA Medical Center
2023

Loyola University Medical Center
2022

Huisarts en Wetenschap
2010-2021

GGD Haaglanden
2020

The susceptibility for various diseases as well the response to treatments differ considerably between men and women. As a basis gender-specific personalized healthcare, an extensive characterization of molecular differences two genders is required. In present study, we conducted large-scale metabolomics analysis 507 metabolic markers measured in serum 1756 participants from German KORA F4 study (903 females 853 males). One-third metabolites show significant males females. A pathway revealed...

10.1007/s11306-015-0829-0 article EN cc-by Metabolomics 2015-08-03

Context Adverse environmental exposures lead to developmental adaptations in fetal life.The influences of maternal physical characteristics and lifestyle habits on firsttrimester the postnatal consequences are not known.Objective To determine risk factors outcomes associated with growth restriction.Design, Setting, Participants Prospective evaluation associations first-trimester crown rump length 1631 mothers a known reliable first day their last menstrual period regular cycle.Subsequently,...

10.1001/jama.2010.78 article EN JAMA 2010-02-09

An age-dependent association between variation at the FTO locus and BMI in children has been suggested. We meta-analyzed associations (rs9939609) samples, aged from early infancy to 13 years, 8 cohorts of European ancestry. found a positive additional minor (A) alleles 5.5 years onwards, but an inverse below age 2.5 years. Modelling median curves for each genotype using LMS method, we that carriers showed lower infancy, earlier adiposity rebound (AR), higher later childhood. Differences by...

10.1371/journal.pgen.1001307 article EN cc-by PLoS Genetics 2011-02-17

Metabolomics has opened new avenues for studying metabolic alterations in type 2 diabetes. While many urine and blood metabolites have been associated individually with diabetes, a complete systems view analysis of dysregulations across multiple biofluids over varying timescales glycaemic control is still lacking.Here we report broad metabolomics study clinical setting, covering 2,178 metabolite measures saliva, plasma from 188 individuals diabetes 181 controls Arab Asian descent. Using...

10.1007/s00125-015-3636-2 article EN cc-by Diabetologia 2015-06-06

The prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing at an alarming rate. Elevated enzymes are a primary reason to refer patients for further testing. However, within the normal range do not exclude presence MASLD. We examined MASLD in middle-aged population with overweight and enzymes. In addition, we accuracy 4 sets noninvasive proxies included 1017 participants from Netherlands epidemiology obesity cohort study body mass index ≥25 kg/m 2...

10.1097/md.0000000000034934 article EN cc-by-nc Medicine 2024-01-05

In most ethnicities at least a quarter of all cases with diabetes is assumed to be undiagnosed. Screening for using saliva has been suggested as an effective approach identify affected individuals.The objective the study was noninvasive metabolic marker type 2 in saliva.In case-control diabetes, we used clinical metabolomics discovery screen diabetes-relevant readouts saliva, blood and urine reference. With combination three platforms based on nontargeted mass spectrometry, examined 2178...

10.1210/jc.2013-3596 article EN The Journal of Clinical Endocrinology & Metabolism 2014-01-14

DNA methylation and blood circulating proteins have been associated with many complex disorders, but the underlying disease-causing mechanisms often remain unclear. Here, we report an epigenome-wide association study of 1123 from 944 participants KORA population replication in a multi-ethnic cohort 344 individuals. We identify 98 CpG-protein associations (pQTMs) at stringent Bonferroni level significance. Overlapping transcriptomics, metabolomics, clinical endpoints suggest implication...

10.1038/s41467-019-13831-w article EN cc-by Nature Communications 2020-01-03
Bram P. Prins Timothy J. Mead Jennifer A. Brody Garðar Sveinbjörnsson Ιωάννα Ντάλλα and 95 more Nathan A. Bihlmeyer Marten van den Berg Jette Bork‐Jensen Stefania Cappellani Stefan van Duijvenboden Nikolai Klena George C. Gabriel Xiaoqin Liu Çağrı Güleç Niels Grarup Jeffrey Haessler Leanne M. Hall Alfonso Iorio Aaron Isaacs Ruifang Li‐Gao Honghuang Lin Yongmei Liu Leo‐Pekka Lyytikäinen Jonathan Marten Hao Mei Martina Müller‐Nurasyid Michele Orini Sandosh Padmanabhan Farid Radmanesh Julia Ramírez Antonietta Robino Molly Schwartz Jessica van Setten Albert V. Smith Niek Verweij Helen R. Warren Stefan Weiß Álvaro Alonso Davíð O. Arnar Michiel L. Bots Rudolf A. de Boer Anna F. Dominiczak Mark Eijgelsheim Patrick T. Ellinor Xiuqing Guo Stephan B. Felix Tamara B. Harris Caroline Hayward Susan R. Heckbert Paul L. Huang J. Wouter Jukema Mika Kähönen Jan A. Kors Pier D. Lambiase Lenore J. Launer Man Li Allan Linneberg Christopher P. Nelson Oluf Pedersen Marco Pérez Annette Peters Ozren Polašek Bruce M. Psaty Olli T. Raitakari Kenneth Rice Jerome I. Rotter Moritz F. Sinner Elsayed Z. Soliman Tim D. Spector Konstantin Strauch Unnur Þorsteinsdóttir Andrew Tinker Stella Trompet André G. Uitterlinden Ilonca Vaartjes Peter van der Meer Uwe Völker Henry Völzke Mélanie Waldenberger James Wilson Zhijun Xie Folkert W. Asselbergs Marcus Dörr Cornelia M. van Duijn Paolo Gasparini Daníel F. Guðbjartsson Vilmundur Guðnason Torben Hansen Stefan Kääb Jørgen K. Kanters Charles Kooperberg Terho Lehtimäki Henry J. Lin Steven A. Lubitz Dennis O. Mook‐Kanamori Francesco J. Conti Christopher Newton‐Cheh Jonathan Rosand Igor Rudan Nilesh J. Samani

Genome-wide association studies conducted on QRS duration, an electrocardiographic measurement associated with heart failure and sudden cardiac death, have led to novel biological insights into function. However, the variants identified fall predominantly in non-coding regions their underlying mechanisms remain unclear. Here, we identify putative functional coding variation changes interval duration by combining Illumina HumanExome BeadChip genotype data from 77,898 participants of European...

10.1186/s13059-018-1457-6 article EN cc-by Genome biology 2018-07-10

Introduction It is crucial to understand the factors that introduce variability before applying metabolomics clinical and biomarker research. Objectives We quantified technical biological of both fasting postprandial metabolite concentrations measured using 1H NMR spectroscopy in plasma samples. Methods In Netherlands Epidemiology Obesity study (n = 6,671), 148 (101 metabolites belonging lipoprotein subclasses) were under states (150 minutes after a mixed liquid meal). Technical was...

10.1371/journal.pone.0218549 article EN cc-by PLoS ONE 2019-06-20
Hanieh Yaghootkar Yiying Zhang Cassandra N. Spracklen Tugce Karaderi Lam Opal Huang and 95 more Jonathan P. Bradfield Claudia Schurmann Rebecca S. Fine Michael Preuß Zoltán Kutalik Laura B. L. Wittemans Yingchang Lu Sophia Metz Sara M. Willems Ruifang Li‐Gao Niels Grarup Shuai Wang Sophie Molnos América A. Sandoval-Zárate Mike A. Nalls Leslie A. Lange Jeffrey Haesser Xiuqing Guo Leo‐Pekka Lyytikäinen Mary F. Feitosa Colleen M. Sitlani Cristina Venturini Anubha Mahajan Tim Kacprowski Carol A. Wang Daniel I. Chasman Najaf Amin Linda Broer Neil Robertson Kristin L. Young Matthew Allison Paul L. Auer Matthias Blüher Judith B. Borja Jette Bork‐Jensen Germán D. Carrasquilla Paraskevi Christofidou Ayşe Demirkan Claudia A. Doege Melissa E. Garcia Mariaelisa Graff Kaiying Guo Hákon Hákonarson Jaeyoung Hong Yii-Der Ida Chen Rebecca D. Jackson Hermina Jakupović Pekka Jousilahti Anne E. Justice Mika Kähönen Jorge R. Kizer Jennifer Kriebel Charles A. LeDuc Jin Li Lars Lind Jian’an Luan David A. Mackey Massimo Mangino Satu Männistö Jayne F. Martin Carli Carolina Medina‐Gómez Dennis O. Mook‐Kanamori Andrew P. Morris Renée de Mutsert Matthias Nauck Ivana Nedeljković Craig E. Pennell Arund D. Pradhan Bruce M. Psaty Olli T. Raitakari Robert A. Scott Tea Skaaby Konstantin Strauch Kent D. Taylor Alexander Teumer André G. Uitterlinden Ying Wu Jie Yao Mark Walker Kari E. North Péter Kovács M. Arfan Ikram Cornelia M. van Duijn Paul M. Ridker Stephen J. Lye Georg Homuth Erik Ingelsson Tim D. Spector Barbara McKnight Michael A. Province Terho Lehtimäki Linda S. Adair Jerome I. Rotter Alexander P. Reiner James G. Wilson

Leptin influences food intake by informing the brain about status of body fat stores. Rare LEP mutations associated with congenital leptin deficiency cause severe early-onset obesity that can be mitigated administering leptin. However, role genetic regulation in polygenic remains poorly understood. We performed an exome-based analysis up to 57,232 individuals diverse ancestries identify variants influence adiposity-adjusted concentrations. five novel variants, including four missense LEP,...

10.2337/db20-0070 article EN Diabetes 2020-09-11

Early weight gain is associated with an increased risk of obesity. It not known whether rapid in foetal life and infancy also abdominal adiposity. We examined the associations postnatal growth characteristics fat mass at age 2 years.This study was performed 481 children participating a prospective cohort from early onward.Foetal second third trimester, birth years were related to (subcutaneous distance area, preperitoneal area) measured by ultrasound years.Foetal subcutaneous mass. Estimated...

10.1111/j.1365-2265.2009.03708.x article EN Clinical Endocrinology 2009-09-21

Most studies investigating human metabolomics measurements are limited to a single biofluid, most often blood or urine. An organism's biochemical pool, however, comprises complex transboundary relationships, which can only be understood by metabolic interactions and physiological processes spanning multiple parts of the body. Therefore, we here propose data-driven network-based approach generate an integrated picture associations over fluids. We performed analysis 2251 metabolites measured...

10.1021/pr501130a article EN Journal of Proteome Research 2014-12-01

Recently, five branched-chain and aromatic amino acids were shown to be associated with the risk of developing type 2 diabetes (T2D).We set out examine whether are also development hypertriglyceridemia.We determined serum concentrations 1,125 individuals KORA S4 baseline study, for which follow-up data available at F4 7 years later. After exclusion hypertriglyceridemia (defined as having a fasting triglyceride level above 1.70 mmol/L) baseline, 755 subjects remained analyses.Increased levels...

10.1007/s40618-013-0044-7 article EN cc-by Journal of Endocrinological Investigation 2014-01-08
Amand F. Schmidt Michael V. Holmes David Preiss Daniel I. Swerdlow Spiros Denaxas and 95 more Ghazaleh Fatemifar Rupert Faraway Chris Finan Dennis Valentine Zammy Fairhurst-Hunter Fernando Pires Hartwig Bernardo Lessa Horta Elina Hyppönen Christine Power Max Moldovan Erik Van Iperen Kees Hovingh Ilja Demuth Kristina Norman Elisabeth Steinhagen‐Thiessen Juri Demuth Lars Bertram Christina M. Lill Stefan Coassin Johann Willeit Stefan Kiechl Karin Willeit Dan Mason John Wright Richard Morris Goya Wanamethee Peter H. Whincup Yoav Ben‐Shlomo Stela McLachlan Jackie F. Price Mika Kivimäki Catherine Welch Adelaida Sánchez-Gálvez Pedro Marques‐Vidal Andrew Nicolaides Andrie G. Panayiotou N. Charlotte Onland‐Moret Yvonne T. van der Schouw Giuseppe Matullo Giovanni Fiorito Simonetta Guarrera Carlotta Sacerdote Nicholas J. Wareham Claudia Langenberg Robert A. Scott Jian’an Luan Martin Bobák Sofia Malyutina Andrzej Pająk Růžena Kubínová Abdonas Tamošiūnas Hynek Pikhart Niels Grarup Oluf Pedersen Torben Hansen Allan Linneberg Tine Jess Jackie A. Cooper Steve E. Humphries Murray H. Brilliant Terrie Kitchner Hákon Hákonarson David Carrell Catherine A. McCarty Kirchner H. Lester Eric B. Larson David R. Crosslin Mariza de Andrade Dan M. Roden Joshua C. Denny Cara L. Carty Stephen Hancock John Attia Elizabeth G. Holliday Rodney J. Scott Peter W. Schofield Martin O’Donnell Salim Yusuf Michael Chong Guillaume Paré Pim van der Harst M. Abdullah Said Ruben N. Eppinga Niek Verweij Harold Snieder Tim Christen Dennis O. Mook‐Kanamori Stefan Gustafsson Lars Lind Erik Ingelsson Raha Pazoki Oscar H. Franco Albert Hofman André G. Uitterlinden Abbas Dehghan

Abstract Background We characterised the phenotypic consequence of genetic variation at PCSK9 locus and compared findings with recent trials pharmacological inhibitors PCSK9. Methods Published individual participant level data (300,000+ participants) were combined to construct a weighted gene-centric score (GS). Seventeen randomized placebo controlled inhibitor included, providing on 79,578 participants. Results scaled one mmol/L lower LDL-C concentration. The GS (comprising 4 SNPs)...

10.1186/s12872-019-1187-z article EN cc-by BMC Cardiovascular Disorders 2019-10-29
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