Lauren B. Gunderson

Most-cited papers

1. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

   V. Salpietro, C. Dixon, Hui Guo, O. Bello +234 more

   2019Nature Communications227 citations Open access

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2. Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

   M. Cousin, Blake A. Creighton, Keith A. Breau, R. Spillmann +70 more

   2021Nature Genetics94 citations Open access

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3. NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

   H. Stamberger, T. Hammer, E. Gardella, D. R. Vlaskamp +81 more

   2020Genetics in Medicine56 citations Open access

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4. A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome

   Theodore G. Drivas, Dong Li, Divya R. Nair, J. Alaimo +61 more

   2020European Journal of Human Genetics47 citations Open access

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5. Impact of integrated translational research on clinical exome sequencing

   E. W. Klee, M. Cousin, F. Vairo, Joel A. Morales-Rosado +56 more

   2020Genetics in Medicine35 citations Open access

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6. Profound intellectual disability caused by homozygous TRAPPC9 pathogenic variant in a man from Malta

   K. Wilton, Lauren B. Gunderson, L. Hasadsri, C. P. Wood +1 more

   2020Molecular Genetics & Genomic Medicine23 citations Open access

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7. Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder

   Laura E. Schultz-Rogers, Ikuo Masuho, F. Vairo, Christopher T. Schmitz +7 more

   2020Molecular Genetics & Genomic Medicine15 citations Open access

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8. Complex phenotypes in ALG12-congenital disorder of glycosylation (ALG12-CDG): Case series and review of the literature.

   Shawn Tahata, Lauren B. Gunderson, Brendan Lanpher, E. Morava

   2019Molecular Genetics and Metabolism15 citations

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9. Jumonji domain containing 1C (JMJD1C) sequence variants in seven patients with autism spectrum disorder, intellectual disability and seizures.

   A. Slavotinek, J. V. van Hagen, Louisa Kalsner, Shashidhar G. Pai +10 more

   2020European Journal of Medical Genetics7 citations Open access

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10. Perspectives on facilitating whole exome sequencing for international patients at Mayo Clinic

    Nicole L. Bertsch, Katherine E. Agre, Sarah Ewing, Lauren B. Gunderson +2 more

    2019Journal of Genetic Counseling0 citations

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