Girirajan S - Search Results

1

Missing heritability and where to find it.

Girirajan S. Girirajan S. Genome Biol. 2017 May 11;18(1):89. doi: 10.1186/s13059-017-1227-x. Genome Biol. 2017. PMID: 28494787 Free PMC article.

2

Genomic disorders: complexity at multiple levels.

Girirajan S. Girirajan S. Genome Med. 2013 May 29;5(5):43. doi: 10.1186/gm447. eCollection 2013. Genome Med. 2013. PMID: 23731576 Free PMC article.

3

Mapping a shared genetic basis for neurodevelopmental disorders.

Jensen M, Girirajan S. Jensen M, et al. Among authors: girirajan s. Genome Med. 2017 Dec 14;9(1):109. doi: 10.1186/s13073-017-0503-4. Genome Med. 2017. PMID: 29241461 Free PMC article.

4

A machine-learning approach for accurate detection of copy number variants from exome sequencing.

Pounraja VK, Jayakar G, Jensen M, Kelkar N, Girirajan S. Pounraja VK, et al. Among authors: girirajan s. Genome Res. 2019 Jul;29(7):1134-1143. doi: 10.1101/gr.245928.118. Epub 2019 Jun 6. Genome Res. 2019. PMID: 31171634 Free PMC article.

5

Genetic subtypes, allelic effects, and convergent neurodevelopmental mechanisms.

Das M, Girirajan S. Das M, et al. Among authors: girirajan s. Genome Med. 2021 Jun 7;13(1):99. doi: 10.1186/s13073-021-00913-y. Genome Med. 2021. PMID: 34099044 Free PMC article. Review.

6

Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion.

Jensen M, Tyryshkina A, Pizzo L, Smolen C, Das M, Huber E, Krishnan A, Girirajan S. Jensen M, et al. Among authors: girirajan s. Genome Med. 2021 Oct 18;13(1):163. doi: 10.1186/s13073-021-00982-z. Genome Med. 2021. PMID: 34657631 Free PMC article.

7

Lessons from model organisms: phenotypic robustness and missing heritability in complex disease.

Queitsch C, Carlson KD, Girirajan S. Queitsch C, et al. Among authors: girirajan s. PLoS Genet. 2012;8(11):e1003041. doi: 10.1371/journal.pgen.1003041. Epub 2012 Nov 15. PLoS Genet. 2012. PMID: 23166511 Free PMC article.

8

An assessment of sex bias in neurodevelopmental disorders.

Polyak A, Rosenfeld JA, Girirajan S. Polyak A, et al. Among authors: girirajan s. Genome Med. 2015 Aug 27;7(1):94. doi: 10.1186/s13073-015-0216-5. Genome Med. 2015. PMID: 26307204 Free PMC article.

9

Novel metrics to measure coverage in whole exome sequencing datasets reveal local and global non-uniformity.

Wang Q, Shashikant CS, Jensen M, Altman NS, Girirajan S. Wang Q, et al. Among authors: girirajan s. Sci Rep. 2017 Apr 13;7(1):885. doi: 10.1038/s41598-017-01005-x. Sci Rep. 2017. PMID: 28408746 Free PMC article.

10

Molecular basis for phenotypic similarity of genetic disorders.

Pounraja VK, Girirajan S. Pounraja VK, et al. Among authors: girirajan s. Genome Med. 2019 Apr 23;11(1):24. doi: 10.1186/s13073-019-0641-y. Genome Med. 2019. PMID: 31014384 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

108 results

Search Page

Filters