Joost Verlouw

2023

OTTERS: a powerful TWAS framework leveraging summary-level reference data

Dai, Q., Zhou, G., eQTLgen Consortium, Zhao, H., Võsa, U., Franke, L., Battle, A., Teumer, A., Lehtimäki, T., Raitakari, O. T., Esko, T., Agbessi, M., Ahsan, H., Alves, I., Andiappan, A. K., Arindrarto, W., Awadalla, P., Battle, A., Beutner, F., Jan Bonder, M., & 31 othersBoomsma, D. I., Christiansen, M. W., Claringbould, A., Deelen, P., Favé, M. J., Frayling, T., Gharib, S. A., Gibson, G., Heijmans, B. T., Hemani, G., Jansen, R., Kähönen, M., Kalnapenkis, A., Kasela, S., Kettunen, J., Kim, Y., Kirsten, H., Kovacs, P., Krohn, K., Kronberg, J., Kukushkina, V., Kutalik, Z., Lee, B., Loeffler, M., Marigorta, U. M., Mei, H., Scholz, M., van Meurs, J., Verlouw, J., Yang, J. & Yang, J., 7 Mar 2023, In: Nature Communications. 14, 1, 1271.

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2022

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

Battle, S. L., Puiu, D., TOPMed mtDNA Working Group, Verlouw, J., Broer, L., Boerwinkle, E., Taylor, K. D., Rotter, J. I., Rich, S. S., Grove, M. L., Pankratz, N., Fetterman, J. L., Liu, C. & Arking, D. E., 31 Mar 2022, In: NAR Genomics and Bioinformatics. 4, 2, lqac034.

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6 Citations (Scopus)

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Whole Exome Sequencing in Two Southeast Asian Families With Atypical Femur Fractures

Zhou, W., Nguyen, H. H., van de Laarschot, D. M., Howe, T. S., Koh, J. S. B., Milat, F., van Rooij, J. G. J., Verlouw, J. A. M., van der Eerden, B. C. J., Stevenson, M., Thakker, R. V., Zillikens, M. C. & Ebeling, P. R., Aug 2022, In: JBMR Plus. 6, 8, e10659.

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1 Citation (Scopus)

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2021

A comparison of genotyping arrays

Verlouw, J. A. M., Clemens, E., de Vries, J. H., Zolk, O., Verkerk, A. J. M. H., am Zehnhoff-Dinnesen, A., Medina-Gomez, C., Lanvers-Kaminsky, C., Rivadeneira, F., Langer, T., van Meurs, J. B. J., van den Heuvel-Eibrink, M. M., Uitterlinden, A. G. & Broer, L., Nov 2021, In: European Journal of Human Genetics. 29, 11, p. 1611-1624 14 p.

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25 Citations (Scopus)

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Composition of cutaneous bacterial microbiome in seborrheic dermatitis patients: A cross-sectional study

Sanders, M. G. H., Nijsten, T., Verlouw, J., Kraaij, R. & Pardo Cortes, L., 24 May 2021, In: PLoS ONE. 16, 5 May, e0251136.

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3 Citations (Scopus)

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Congenital hypopituitarism in two brothers with a duplication of the ‘acrogigantism gene’ GPR101: clinical findings and review of the literature

Elizabeth, M. S. M., Verkerk, A. J. M. H., Hokken-Koelega, A. C. S., Verlouw, J. A. M., Argente, J., Pfaeffle, R., Neggers, S. J. C. M. M., Visser, J. A. & de Graaff, L. C. G., Apr 2021, In: Pituitary. 24, 2, p. 229-241 13 p.

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2 Citations (Scopus)

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Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour

Mills, M. C., Tropf, F. C., eQTLgen Consortium, BIOS Consortium, Human Reproductive Behaviour Consortium, Brazel, D. M., van Zuydam, N., Vaez, A., Perry, J. R. B., Pers, TH., Snieder, H., Ong, K. K., den Hoed, M., Barban, N. & Day, F. R., 1 Jul 2021, In: Nature Human Behaviour. 17 p.

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29 Citations (Scopus)

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Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

Võsa, U., Claringbould, A., BIOS Consortium, i2QTL Consortium, Westra, H. J., Bonder, M. J., Deelen, P., Zeng, B., Kirsten, H., Saha, A., Kreuzhuber, R., Yazar, S., Brugge, H., Oelen, R., de Vries, D. H., van der Wijst, M. G. P., Kasela, S., Pervjakova, N., Alves, I., Favé, M. J., & 35 othersAgbessi, M., Christiansen, M. W., Jansen, R., Seppälä, I., Tong, L., Teumer, A., Schramm, K., Hemani, G., Verlouw, J., Yaghootkar, H., Sönmez Flitman, R., Brown, A., Kukushkina, V., Kalnapenkis, A., Rüeger, S., Porcu, E., Kronberg, J., Kettunen, J., Lee, B., Zhang, F., Qi, T., Hernandez, J. A., Arindrarto, W., Beutner, F., Dmitrieva, J., Elansary, M., Fairfax, B. P., Georges, M., Heijmans, B. T., Mei, H., Yang, J., Scholz, M., van Meurs, J., Esko, T. & Franke, L., 1 Sept 2021, In: Nature Genetics. 53, 9, p. 1300-1310 11 p.

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267 Citations (Scopus)

2020

Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time

van Rooij, J., Arp, P., Broer, L., Verlouw, J., van Rooij, FJA., Kraaij, R., Uitterlinden, A. & Verkerk, A., 2020, In: Genetics in Medicine. 22, 11, p. 1812-1820 9 p.

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20 Citations (Scopus)

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Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies

Hammerschlag, A. R., eQTLgen Consortium, BIOS Consortium, Byrne, E. M. & Bartels, M., 15 Sept 2020, In: Biological Psychiatry. 88, 6, p. 470-479 10 p.

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11 Citations (Scopus)

Unique near-complete deletion of GLI2 in a patient with combined pituitary hormone deficiency and post-axial polydactyly

Elizabeth, MSM., Verkerk, A., Hokken - Koelega, A., Verlouw, J., Argente, J., Pfaeffle, R., Visser, T., Peeters, R. & de Graaff, L., 2020, In: Growth Hormone and IGF Research. 50, p. 35-41 7 p.

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7 Citations (Scopus)

2019

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

23andMe Inc., eQTLgen Consortium, International Cannabis Consortium, Social Science Genetic Association Consortium, Karlsson Linnér, R., Biroli, P., Kong, E., Meddens, S. F. W., Wedow, R., Fontana, M. A., Lebreton, M., Tino, S. P., Abdellaoui, A., Hammerschlag, A. R., Nivard, M. G., Okbay, A., Rietveld, C. A., Timshel, P. N., Trzaskowski, M., Vlaming, R. D., & 34 othersZünd, C. L., Bao, Y., Buzdugan, L., Caplin, A. H., Chen, C. Y., Eibich, P., Fontanillas, P., Gonzalez, J. R., Joshi, P. K., Karhunen, V., Kleinman, A., Levin, R. Z., Lill, C. M., Taskesen, E., Heijmans, B., Jansen, R., Scholz, M., Teumer, A., Meurs, J. V., Verlouw, J., Yang, J., Lee, S. J. V. D., Poot, R. A., Verweij, N., Zhao, W., Amin, N., Hottenga, J. J., Schmidt, H., Duijn, C. M. V., Groenen, P. J. F., Posthuma, D., Tiemeier, H., Uitterlinden, A. G. & Ikram, M. A., 1 Feb 2019, In: Nature Genetics. 51, 2, p. 245-257 13 p.

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305 Citations (Scopus)

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2018

Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

Xue, A., Wu, Y., Zhu, Z., Verlouw, J., van Meurs, J., Zhang, F., Kemper, KE. & Zheng, Z., 2018, In: Nature Communications. 9, 1, 2941.

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388 Citations (Scopus)

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Identifying gene targets for brain-related traits using transcriptomic and methylomic data from blood

Qi, T., Wu, Y., Zeng, J., Zhang, F., Xue, A., van Meurs, J., Verlouw, J., Mcrae, AF. & Yang, J., 2018, In: Nature Communications. 9, 1, 2282.

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173 Citations (Scopus)

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Whole-Exome Sequencing in Age-Related Macular Degeneration Identifies Rare Variants in COL8A1, a Component of Bruch's Membrane

Corominas, J., Colijn, A., Geerlings, MJ., Pauper, M., Bakker, B., Amin, N., Motta, LL., Kersten, E., Garanto, A., Verlouw, J., van Rooij, J., Kraaij, R., Jong, PHP., Hofman, B., Vingerling, H., Schick, T., Fauser, S., de Jong, EK., Duijn, C., Hoyng, CB., & 2 othersKlaver, C. & Hollander, AI., 2018, In: Ophthalmology. 125, 9, p. 1433-1443 11 p.

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34 Citations (Scopus)

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Joost Verlouw

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