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Quinten, Laura [Author]

Continuity with Future Selves in Delinquent, Financial, and Health-Related Decision Making

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Bonn: Universitäts- und Landesbibliothek Bonn, 2020
Oberlader, Verena A.; Quinten, Laura; Banse, Rainer; Volbert, Renate; Schmidt, Alexander F.; Schönbrodt, Felix D.

Validity of content‐based techniques for credibility assessment—How telling is an extended meta‐analysis taking research bias into account?

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Wiley, 2021

Published in: Applied Cognitive Psychology
Oberlader, Verena A.; Naefgen, Christoph; Koppehele-Gossel, Judith; Quinten, Laura; Banse, Rainer; Schmidt, Alexander F.

Validity of content-based techniques to distinguish true and fabricated statements: A meta-analysis

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American Psychological Association (APA), 2016

Published in: Law and Human Behavior
Akkerman, Quinten A.; Martínez-Sarti, Laura; Goldoni, Luca; Imran, Muhammad; Baranov, Dmitry; Bolink, Henk J.; Palazon, Francisco; Manna, Liberato

Molecular Iodine for a General Synthesis of Binary and Ternary Inorganic and Hybrid Organic–Inorganic Iodide Nanocrystals

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American Chemical Society (ACS), 2018

Published in: Chemistry of Materials
Mol, Jan‐Quinten; van Tuijl, Julia; Bekkering, Siroon; Rodwell, Laura; Pop, Gheorghe A. M.; Netea, Mihai G.; van Royen, Niels; Riksen, Niels P.; El Messaoudi, Saloua

Two‐Week Interruption of Statin Therapy Results in an Exaggerated Inflammatory Monocyte Phenotype in Young Patients With Myocardial Infarction Without Standard Modifiable Risk Factors

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Ovid Technologies (Wolters Kluwer Health), 2024

Published in: Journal of the American Heart Association
Wolf, Nicole; van Weissenbruch, Mirjam; Stam, Cornelie; Weiss, Janneke; Waisfisz, Quinten; Kevelam, Sietske; Bugiani, Mariana; van de Kamp, Jiddeke; van der Knaap, Marjo; van de Pol, Laura

Early-Onset Severe Encephalopathy with Epilepsy: The BRAT1 Gene Should Be Added to the List of Causes

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Georg Thieme Verlag KG, 2015

Published in: Neuropediatrics
Mesnage, Robin; Teixeira, Maxime; Mandrioli, Daniele; Falcioni, Laura; Ibragim, Mariam; Ducarmon, Quinten Raymond; Zwittink, Romy Daniëlle; Amiel, Caroline; Panoff, Jean-Michel; Bourne, Emma; Savage, Emanuel; Mein, Charles A.; Belpoggi, Fiorella; Antoniou, Michael N.

Multi-omics phenotyping of the gut-liver axis reveals metabolic perturbations from a low-dose pesticide mixture in rats

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Springer Science and Business Media LLC, 2021

Published in: Communications Biology
Mesnage, Robin; Teixeira, Maxime; Mandrioli, Daniele; Falcioni, Laura; Ducarmon, Quinten Raymond; Zwittink, Romy Daniëlle; Mazzacuva, Francesca; Caldwell, Anna; Halket, John; Amiel, Caroline; Panoff, Jean-Michel; Belpoggi, Fiorella; Antoniou, Michael Nicolas

Use of Shotgun Metagenomics and Metabolomics to Evaluate the Impact of Glyphosate or Roundup MON 52276 on the Gut Microbiota and Serum Metabolome of Sprague-Dawley Rats

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Environmental Health Perspectives, 2021

Published in: Environmental Health Perspectives
Akkerman, Quinten A.; Motti, Silvia Genaro; Srimath Kandada, Ajay Ram; Mosconi, Edoardo; D’Innocenzo, Valerio; Bertoni, Giovanni; Marras, Sergio; Kamino, Brett A.; Miranda, Laura; De Angelis, Filippo; Petrozza, Annamaria; Prato, Mirko; Manna, Liberato

Solution Synthesis Approach to Colloidal Cesium Lead Halide Perovskite Nanoplatelets with Monolayer-Level Thickness Control

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American Chemical Society (ACS), 2016

Published in: Journal of the American Chemical Society
Waisfisz, Quinten; de Winter, Johan P.; Kruyt, Frank A. E.; de Groot, Jan; van der Weel, Laura; Dijkmans, Lonneke M.; Zhi, Yu; Arwert, Fré; Scheper, Rik J.; Youssoufian, Hagop; Hoatlin, Maureen E.; Joenje, Hans

A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA

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Proceedings of the National Academy of Sciences, 1999

Published in: Proceedings of the National Academy of Sciences
Waisfisz, Quinten; De Winter, Johan P.; de Groot, Jan; van der Weel, Laura; Dijkmans, Lonneke M.; Zhi, Yu; Arwert, Fre; Scheper, Rik J.; Youssoufian, Hagop; Hoatlin, Maureen E.; Joenje, Hans

A Physical Complex of the Fanconi Anemia Proteins FANCG/XRCC9 and FANCA

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National Academy of Sciences of the United States of America, 1999

Published in: Proceedings of the National Academy of Sciences of the United States of America
Mak, Anne Linde; Augustijn, Quinten J. J.; Heymann, Clément J. F.; Havik, Stefan; Verdoes, Xanthe; Rios-Morales, Melany; Bosmans, Laura A.; Verheij, Joanne; Meijnikman, Abraham S.; de Jonge, Patrick A.; Herrema, Hilde; de Vos, Willem M.; Nieuwdorp, Max; Grefhorst, Aldo; Holleboom, Adriaan G.

Anaerobutyricum soehngenii Reduces Hepatic Lipogenic Pathways and Increases Intestinal Gluconeogenic Gene Expression in Metabolic-Dysfunction-Associated Steatotic Liver Disease (MASLD) Mice

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MDPI AG, 2024

Published in: International Journal of Molecular Sciences
Mol, Jan-Quinten; van Tuijl, Julia; Bekkering, Siroon; van der Heijden, Charlotte D.C.C.; Damen, Sander A.J.; Cossins, Benjamin C.; van Emst, Liesbeth; Nielen, Tim M.; Rodwell, Laura; Li, Yang; Pop, Gheorghe A.M.; Netea, Mihai G.; van Royen, Niels; Riksen, Niels P.; El Messaoudi, Saloua

Peripheral blood mononuclear cell hyperresponsiveness in patients with premature myocardial infarction without traditional risk factors

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Elsevier BV, 2023

Published in: iScience
de Winter, Johan P.; Rooimans, Martin A.; van der Weel, Laura; van Berkel, Carola G.M.; Alon, Noa; Bosnoyan-Collins, Lucine; de Groot, Jan; Zhi, Yu; Waisfisz, Quinten; Pronk, Jan C.; Arwert, Fré; Mathew, Christopher G.; Scheper, Rik J.; Hoatlin, Maureen E.; Buchwald, Manuel; Joenje, Hans

The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

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Springer Science and Business Media LLC, 2000

Published in: Nature Genetics
de Winter, Johan P.; Leveille, France; van Berkel, Carola G. M.; Rooimans, Martin A.; van der Weel, Laura; Steltenpool, Jurgen; Demuth, Ilja; Morgan, Neil V.; Alon, Noa; Bosnoyan‐Collins, Lucine; Lightfoot, Jeff; Leegwater, Peter A.; Waisfisz, Quinten; Komatsu, Kenshi; Arwert, Fre; Pronk, Jan C.; Mathew, Christopher G.; Digweed, Martin; Buchwald, Manuel; Joenje, Hans

Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

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Elsevier BV, 2000

Published in: The American Journal of Human Genetics
de Winter, Johan P.; Léveillé, France; van Berkel, Carola G.M.; Rooimans, Martin A.; van der Weel, Laura; Steltenpool, Jurgen; Demuth, Ilja; Morgan, Neil V.; Alon, Noa; Bosnoyan-Collins, Lucine; Lightfoot, Jeff; Leegwater, Peter A.; Waisfisz, Quinten; Komatsu, Kenshi; Arwert, Fré; Pronk, Jan C.; Mathew, Christopher G.; Digweed, Martin; Buchwald, Manuel; Joenje, Hans

Isolation of a cDNA Representing the Fanconi Anemia Complementation Group E Gene

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Elsevier BV, 2000

Published in: The American Journal of Human Genetics
Gräf, Stefan; Haimel, Matthias; Bleda, Marta; Hadinnapola, Charaka; Southgate, Laura; Li, Wei; Hodgson, Joshua; Liu, Bin; Salmon, Richard M.; Southwood, Mark; Machado, Rajiv D.; Martin, Jennifer M.; Treacy, Carmen M.; Yates, Katherine; Daugherty, Louise C.; Shamardina, Olga; Whitehorn, Deborah; Holden, Simon; Aldred, Micheala; Bogaard, Harm J.; Church, Colin; Coghlan, Gerry; Condliffe, Robin; Corris, Paul A.; [...]

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

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Springer Science and Business Media LLC, 2018

Published in: Nature Communications
Motta, Marialetizia; Pannone, Luca; Pantaleoni, Francesca; Bocchinfuso, Gianfranco; Radio, Francesca Clementina; Cecchetti, Serena; Ciolfi, Andrea; Di Rocco, Martina; Elting, Mariet W.; Brilstra, Eva H.; Boni, Stefania; Mazzanti, Laura; Tamburrino, Federica; Walsh, Larry; Payne, Katelyn; Fernández-Jaén, Alberto; Ganapathi, Mythily; Chung, Wendy K.; Grange, Dorothy K.; Dave-Wala, Ashita; Reshmi, Shalini C.; Bartholomew, Dennis W.; Mouhlas, Danielle; Carpentieri, Giovanna; [...]

Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum

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Elsevier BV, 2020

Published in: The American Journal of Human Genetics
Fliedner, Anna; Kirchner, Philipp; Wiesener, Antje; van de Beek, Irma; Waisfisz, Quinten; van Haelst, Mieke; Scott, Daryl A.; Lalani, Seema R.; Rosenfeld, Jill A.; Azamian, Mahshid S.; Xia, Fan; Dutra-Clarke, Marina; Martinez-Agosto, Julian A.; Lee, Hane; Noh, Grace J.; Lippa, Natalie; Alkelai, Anna; Aggarwal, Vimla; Agre, Katherine E.; Gavrilova, Ralitza; Mirzaa, Ghayda M.; Straussberg, Rachel; Cohen, Rony; Horist, Brooke; [...]

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

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Elsevier BV, 2020

Published in: The American Journal of Human Genetics
Stephenson, Sarah E.M.; Costain, Gregory; Blok, Laura E.R.; Silk, Michael A.; Nguyen, Thanh Binh; Dong, Xiaomin; Alhuzaimi, Dana E.; Dowling, James J.; Walker, Susan; Amburgey, Kimberly; Hayeems, Robin Z.; Rodan, Lance H.; Schwartz, Marc A.; Picker, Jonathan; Lynch, Sally A.; Gupta, Aditi; Rasmussen, Kristen J.; Schimmenti, Lisa A.; Klee, Eric W.; Niu, Zhiyv; Agre, Katherine E.; Chilton, Ilana; Chung, Wendy K.; Revah-Politi, Anya; [...]

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

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Elsevier BV, 2022

Published in: The American Journal of Human Genetics

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