Author

Kristin Lindstrom

Phoenix Children's Hospital

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Research Focus:gene regulatory network inference· 2 Approach:statistical model· 2 Research Focus:benchmarking· 1 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Organism:Drosophila· 1 Approach:experimental assay· 1

Frequent Co-Authors

A. GélotiD· 1 shared Alfonso RepresaiD· 1 shared Alina KurolapiD· 1 shared Amy Siemon· 1 shared Andreas BosioiD· 1 shared Antoine de ChevignyiD· 1 shared Arie van HaeringeniD· 1 shared Arthur Loubat· 1 shared

Activity by Year

2020-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperNeuroscience

A. GélotORCID

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2 papers

Recent·Most cited

Pathogenic variants in SMARCA5, a chromatin remodeler, cause a range of syndromic neurodevelopmental features

Dong Li, Qin Wang, Naihua Natalie Gong, Alina Kurolap, Hagit Baris Feldman, Nikolas Boy, Melanie Brügger, Katheryn Grand, Kirsty M. McWalter, María J. Guillen Sacoto, Emma L. Wakeling, Jane A. Hurst, Michael March, Elizabeth J. K. Bhoj, Małgorzata J.M. Nowaczyk, , Hakon H. Hakonarson

The paper identifies pathogenic variants in SMARCA5 as a cause of a neurodevelopmental syndrome with mild facial dysmorphia and developmental delay.

Science Advances · May 12, 2021Peer-reviewedGenetic & Genomic Medicine

Disruption of the transcription factor NEUROD2 causes an autism syndrome via cell-autonomous defects in cortical projection neurons

Karen Runge, Rémi Mathieu, Stéphane Bugeon, Sahra Lafi, Corinne Beurrier, Surajit Sahu, Fabienne Schaller, Arthur Loubat, Léonard Hérault, Stéphane Gaillard, Mélanie Cahuc, Emilie Pallesi‐Pocachard, Aurélie Montheil, Andreas Bosio, Jill Anne Rosenfeld, , Antoine de Chevigny

This study identifies NEUROD2 mutations linked to ASD and intellectual disability, showing their role in cortical development and function through mouse models.

bioRxiv · Feb 14, 2020 · PreprintNeuroscience