Publications by authors named "Sandra Imholz"

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Next-generation Sequencing and Other Second Tier Tests in Newborn Screening for (X-linked) Agammaglobulinemia.
Maartje Blom, Annelotte J Duintjer, Ingrid Pico-Knijnenburg, Sandra Imholz, Sahila Balkassmi

J Clin Immunol· November 2025

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Comparing DNA Isolation and Preparation Protocols for Dried Blood Spots in the Context of Genomic Newborn Screening.
Annelotte J Duintjer, Sandra Imholz, Ingrid Pico-Knijnenburg, Adinda Heuperman, Hennie Hodemaekers

Int J Neonatal Screen· September 2025

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High protein intake causes gene-length-dependent transcriptional decline, shortens lifespan and accelerates ageing in progeroid DNA repair-deficient mice.
Ivar van Galen, Maria B Birkisdóttir, Rutger A Ozinga, Renata M C Brandt, Sander Barnhoorn, Sandra Imholz

NPJ Metab Health Dis· May 2025

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Corrigendum: The use of progeroid DNA repair-deficient mice for assessing anti-aging compounds, illustrating the benefits of nicotinamide riboside.
María B Birkisdóttir, Ivar van Galen, Renata M C Brandt, Sander Barnhoorn, Nicole van Vliet, Sandra Imholz

Front Aging· November 2022

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The use of progeroid DNA repair-deficient mice for assessing anti-aging compounds, illustrating the benefits of nicotinamide riboside.
María B Birkisdóttir, Ivar van Galen, Renata M C Brandt, Sander Barnhoorn, Nicole van Vliet, Sandra Imholz

Front Aging· October 2022

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Second Tier Testing to Reduce the Number of Non-actionable Secondary Findings and False-Positive Referrals in Newborn Screening for Severe Combined Immunodeficiency.
Maartje Blom, Ingrid Pico-Knijnenburg, Sandra Imholz, Lotte Vissers, Janika Schulze

J Clin Immunol· November 2021

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Compromised DNA Repair Promotes the Accumulation of Regulatory T Cells With an Aging-Related Phenotype and Responsiveness.
Daan K J Pieren, Noortje A M Smits, Sandra Imholz, Bhawani Nagarajah, Conny T van Oostrom

Front Aging· May 2021

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Unlike dietary restriction, rapamycin fails to extend lifespan and reduce transcription stress in progeroid DNA repair-deficient mice.
María B Birkisdóttir, Dick Jaarsma, Renata M C Brandt, Sander Barnhoorn, Nicole van Vliet, Sandra Imholz

Aging Cell· February 2021

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Going Back and Forth: Episomal Vector Reprogramming of Peripheral Blood Mononuclear Cells to Induced Pluripotent Stem Cells and Subsequent Differentiation into Cardiomyocytes and Neuron-Astrocyte Co-cultures.
Victoria C de Leeuw, Conny T M van Oostrom, Sandra Imholz, Aldert H Piersma, Ellen V S Hessel

Cell Reprogram· December 2020

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Antibody and Local Cytokine Response to Respiratory Syncytial Virus Infection in Community-Dwelling Older Adults.
Xiao Yu, Anke J Lakerveld, Sandra Imholz, Marion Hendriks, Sofie C A Ten Brink

mSphere· September 2020

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Heterosubtypic cross-reactivity of HA1 antibodies to influenza A, with emphasis on nonhuman subtypes (H5N1, H7N7, H9N2).
Dennis E Te Beest, Erwin de Bruin, Sandra Imholz, Marion Koopmans, Michiel van Boven

PLoS One· September 2017

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Discrimination of influenza infection (A/2009 H1N1) from prior exposure by antibody protein microarray analysis.
Dennis te Beest, Erwin de Bruin, Sandra Imholz, Jacco Wallinga, Peter Teunis

PLoS One· April 2016

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Predictive performance of a seven-plex antibody array in prenatal screening for Down Syndrome.
Jeroen L A Pennings, Sandra Imholz, Ilse Zutt, Maria P H Koster, Jacqueline E Siljee

Dis Markers· December 2015

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Comparison of different blood collection, sample matrix, and immunoassay methods in a prenatal screening setting.
Jeroen L A Pennings, Jacqueline E Siljee, Sandra Imholz, Sylwia Kuc, Annemieke de Vries

Dis Markers· April 2015

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Deletion of individual Ku subunits in mice causes an NHEJ-independent phenotype potentially by altering apurinic/apyrimidinic site repair.
Yong Jun Choi, Han Li, Mi Young Son, Xiao-Hong Wang, Jamie L Fornsaglio, Sandra Imholz

PLoS One· November 2014

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Gender-specific genetic associations of polymorphisms in ACE, AKR1C2, FTO and MMP2 with weight gain over a 10-year period.
Freek G Bouwman, Jolanda M A Boer, Sandra Imholz, Ping Wang, W M Monique Verschuren

Genes Nutr· November 2014

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Identification of interleukin-1 beta, but no other inflammatory proteins, as an early onset pre-eclampsia biomarker in first trimester serum by bead-based multiplexed immunoassays.
Jacqueline E Siljee, Esther J Wortelboer, Maria P H Koster, Sandra Imholz, Wendy Rodenburg

Prenat Diagn· December 2013

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Markers of endogenous desaturase activity and risk of coronary heart disease in the CAREMA cohort study.
Yingchang Lu, Anika Vaarhorst, Audrey H H Merry, Martijn E T Dollé, Robert Hovenier, Sandra Imholz

PLoS One· February 2013

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Codon 72 polymorphism (rs1042522) of TP53 is associated with changes in diastolic blood pressure over time.
Erwin Reiling, Valeriya Lyssenko, Jolanda M A Boer, Sandra Imholz, W Monique M Verschuren

Eur J Hum Genet· June 2012

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Literature-based genetic risk scores for coronary heart disease: the Cardiovascular Registry Maastricht (CAREMA) prospective cohort study.
Anika A M Vaarhorst, Yingchang Lu, Bastiaan T Heijmans, Martijn E T Dollé, Stefan Böhringer, Sandra Imholz

Circ Cardiovasc Genet· April 2012

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Quantitative performance of antibody array technology in a prenatal screening setting.
Wendy Rodenburg, Johan H Reimerink, Sandra Imholz, Gert-Jan Godeke, Jeroen L A Pennings

Clin Chem Lab Med· October 2011

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Genetic variants in lipid metabolism are independently associated with multiple features of the metabolic syndrome.
Cécile M Povel, Jolanda M A Boer, Sandra Imholz, Martijn E T Dollé, Edith J M Feskens

Lipids Health Dis· July 2011

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Gene expression profiling in a mouse model identifies fetal liver- and placenta-derived potential biomarkers for Down Syndrome screening.
Jeroen L A Pennings, Wendy Rodenburg, Sandra Imholz, Maria P H Koster, Conny T M van Oostrom

PLoS One· April 2011

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Exploring genetic determinants of plasma total cholesterol levels and their predictive value in a longitudinal study.
Yingchang Lu, Edith J M Feskens, Jolanda M A Boer, Sandra Imholz, W M Monique Verschuren

Atherosclerosis· November 2010

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Dietary n-3 and n-6 polyunsaturated fatty acid intake interacts with FADS1 genetic variation to affect total and HDL-cholesterol concentrations in the Doetinchem Cohort Study.
Yingchang Lu, Edith Jm Feskens, Martijn Et Dollé, Sandra Imholz, Wm Monique Verschuren

Am J Clin Nutr· July 2010

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