# Enhanced utility of family-centered diagnostic exome sequencing with inheritance model–based analysis: results from 500 unselected families with undiagnosed genetic conditions

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/enhanced-utility-of-family-centered-diagnostic-exome-sequencing-with-inheritance/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Kelly D. Farwell,Layla Shahmirzadi,Dima El‐Khechen,Zöe Powis,Elizabeth Chao,Brigette Tippin Davis,Ruth M. Baxter,Wenqi Zeng,Cameron Mroske,Melissa Parra,Stephanie Gandomi,Ira Lu,Xiang Li,Hong Lu,Hsiao‐Mei Lu,David Salvador,David Ruble,Monica Lao,Soren Fischbach,Jennifer X. Wen,Shela Lee,Aaron Elliott,Charles Dunlop,Sha Tang |
| Citations | 472 |
| DOI | 10.1038/gim.2014.154 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | true |
| OA Status | hybrid |
| OA URL | http://www.gimjournal.org/article/S1098360021028641/pdf |
| OpenAlex ID | https://openalex.org/W2005009098 |
| PMID | 25356970 |
| Type | article |
| Year | 2014 |

## Paper authors

- [Sha Tang](https://scholariq.org/researchers/sha-tang/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Genomic variations and chromosomal abnormalities](https://scholariq.org/topics/genomic-variations-and-chromosomal-abnormalities/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.
