Kristina Calli

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 4

Top Topics

Pseudomonas Aeruginosa

Autism Spectrum Disorder

Top Venues

NPJ genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Silas J Y Yip, Kristina Calli, Ying Qiao, Brett Trost, Stephen W Scherer, M E Suzanne Lewis
Complex Autism Spectrum Disorder in a Patient with a Novel De Novo Heterozygous MYT1L Variant. Genes 14 (12) (2023)
Livia O Loureiro, Jennifer L Howe, Miriam S Reuter, Alana Iaboni, Kristina Calli, Delnaz Roshandel, Iva Pritišanac, Alan Moses, Julie D Forman-Kay, Brett Trost, Mehdi Zarrei, Olivia Rennie, Lynette Y S Lau, Christian R Marshall, Siddharth Srivastava, Brianna Godlewski, Elizabeth D Buttermore, Mustafa Sahin, Dean Hartley, Thomas Frazier, Jacob A S Vorstman, Stelios Georgiades, Suzanne M E Lewis, Peter Szatmari, Clarrisa A Lisa Bradley, Anne-Claude Tabet, Marjolaine Willems, Serge Lumbroso, Amélie Piton, James Lespinasse, Richard Delorme, Thomas Bourgeron, Evdokia Anagnostou, Stephen W Scherer
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder. NPJ genomic medicine 6 (1) (2021)