Nordgren, Ann

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

Stessman, H. A. F., Xiong, B., Coe, B. P., Wang, T., Hoekzema, K., Fenckova, M., Kvarnung, M., Gerdts, J., Trinh, S., Cosemans, N., et al. (2017) · Nature Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Jacquemont, S., Reymond, A., Zufferey, F., Harewood, L., Walters, R. G., Kutalik, Z., Martinet, D., Shen, Y., Valsesia, A., Beckmann, N. D., et al. (2011) · Nature

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

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A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP

Helsmoortel, C., Vulto-van Silfhout, A. T., Coe, B. P., Vandeweyer, G., Rooms, L., van den Ende, J., Schuurs-Hoeijmakers, J. H. M., Marcelis, C. L., Willemsen, M. H., Vissers, L. E. L. M., et al. (2014) · Nature Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

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Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S , which Encode Subcomponents C1r and C1s of Complement

Kapferer-Seebacher, I., Pepin, M., Werner, R., Aitman, T. J., Nordgren, A., Stoiber, H., Thielens, N., Gaboriaud, C., Amberger, A., Schossig, A., et al. (2016) · The American Journal of Human Genetics

Complement system in diseasesOral microbiology and periodontitis research

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Gain-of-function mutation of microRNA-140 in human skeletal dysplasia

Grigelioniene, G., Suzuki, H. I., Taylan, F., Mirzamohammadi, F., Borochowitz, Z. U., Ayturk, U. M., Tzur, S., Horemuzova, E., Lindstrand, A., Weis, M. A., et al. (2019) · Nature Medicine

MicroRNA in disease regulationConnective tissue disorders research

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Limitations of Chromosome Classification by Multicolor Karyotyping

Lee, C., Gisselsson, D., Jin, C., Nordgren, A., Ferguson, D. O., Blennow, E., Fletcher, J. A., & Morton, C. C. (2001) · The American Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesPrenatal Screening and Diagnostics

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The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

Bölte, S., Willfors, C., Berggren, S., Norberg, J., Poltrago, L., Mevel, K., Coco, C., Fransson, P., Borg, J., Sitnikov, R., et al. (2014) · Twin Research and Human Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

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Medical history of discordant twins and environmental etiologies of autism

Willfors, C., Carlsson, T., Anderlid, B.-M., Nordgren, A., Kostrzewa, E., Berggren, S., Ronald, A., Kuja-Halkola, R., Tammimies, K., & Bölte, S. (2017) · Translational Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

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