# Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/rare-coding-variation-provides-insight-into-the-genetic-architecture-and/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Jack Fu,F. Kyle Satterstrom,Minshi Peng,Harrison Brand,Ryan L. Collins,Shan Dong,Brie Wamsley,Lambertus Klei,Lily Wang,Stephanie P. Hao,Christine Stevens,Caroline Cusick,Mehrtash Babadi,Eric Banks,Brett Collins,Sheila Dodge,Stacey B. Gabriel,Laura D. Gauthier,Samuel K. Lee,Lindsay Liang,Alicia Ljungdahl,Behrang Mahjani,Laura Sloofman,Andrey N. Smirnov,Mafalda Barbosa,Catalina Betancur,Alfredo Brusco,Brian Hon‐Yin Chung,Edwin H. Cook,Michael L. Cuccaro,Enrico Domenici,Giovanni Battista Ferrero,J. Jay Gargus,Gail E. Herman,Irva Hertz‐Picciotto,Patrı́cia Maciel,Dara S. Manoach,Maria Rita Passos‐Bueno,Antonio M. Persico,Alessandra Renieri,James S. Sutcliffe,Flora Tassone,Elisabetta Trabetti,Gabriele da Silva Campos,Simona Cardaropoli,Diana Carli,Marcus C.Y. Chan,Chiara Fallerini,Elisa Giorgio,Ana Cristina De Sanctis Girardi,Emily Hansen‐Kiss,So Lun Lee,Carla Lintas,Yunin Ludeña,Rachel Nguyen,Lisa Pavinato,Margaret A. Pericak‐Vance,Isaac N. Pessah,Rebecca J. Schmidt,Moyra Smith,Claudia Ismania Samogy Costa,Slavica Trajkova,Jaqueline Y. T. Wang,Mullin H.C. Yu,Branko Aleksić,Mykyta Artomov,Elisa Benetti,Monica Biscaldi-Schafer,Anders D. Børglum,Ángel Carracedo,Andreas G. Chiocchetti,Hilary Coon,Ryan N. Doan,Montse Fernández‐Prieto,Christine M. Freitag,Sherif Gerges,Stephen J. Guter,David M. Hougaard,Christina M. Hultman,Suma Jacob,Miia Kaartinen,Alexander Kolevzon,Itaru Kushima,Terho Lehtimäki,Caterina Lo Rizzo,Nell Maltman,Marianna Manara,Gal Meiri,Idan Menashe,Judith Miller,Nancy J. Minshew,Matthew W. Mosconi,Norio Ozaki,Aarno Palotie,Mara Parellada,Kaija Puura,Abraham Reichenberg,Sven Sandin,Stephen W. Scherer,Sabine Schlitt |
| Citations | 640 |
| DOI | 10.1038/s41588-022-01104-0 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | true |
| OA Status | green |
| OA URL | http://hdl.handle.net/11380/1288701 |
| OpenAlex ID | https://openalex.org/W4293068820 |
| PMID | 35982160 |
| Type | article |
| Year | 2022 |

## Paper authors

- [Irva Hertz‐Picciotto](https://scholariq.org/researchers/irva-hertz-picciotto/)

## Paper primary topic

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)

## Paper topics

- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)
- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

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