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Farrow, Emily G.
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1

Genomic Answers for Kids: Toward more equitable access to g..:

Cohen, Ana S.A. ; Berrios, Courtney D. ; Zion, Tricia N....
The American Journal of Human Genetics.  111 (2024)  5 - p. 825-832 , 2024
Link: https://doi.org/10.1016/..
 
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2

Large-scale mutational analysis identifies UNC93B1 variants..:

Rael, Victoria E. ; Yano, Julian A. ; Huizar, John P....
Journal of Experimental Medicine.  221 (2024)  8 - p. , 2024
Link: https://doi.org/10.1084/..
 
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3

More Than a Decade of Rapid Genomic Sequencing: Where Are W..:

Saunders, Carol J ; Brunelli, Luca ; Deem, Michael J...
Clinical Chemistry.  70 (2024)  4 - p. 577-583 , 2024
Link: https://doi.org/10.1093/..
 
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4

Pangenome graphs improve the analysis of structural variant..:

Groza, Cristian ; Schwendinger-Schreck, Carl ; Cheung, Warren A....
Nature Communications.  15 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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5

Genetic heterogeneity and enrichment of variants in DNA‐rep..:

Awotoye, Waheed ; Whitt, Joseph Craig ; Yoo, Byunggil...
Journal of Oral Pathology & Medicine.  52 (2023)  3 - p. 263-270 , 2023
Link: https://doi.org/10.1111/..
 
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6

Genomic answers for children: Dynamic analyses of >1000 ped..:

Cohen, Ana S.A. ; Farrow, Emily G. ; Abdelmoity, Ahmed T....
Genetics in Medicine.  24 (2022)  6 - p. 1336-1348 , 2022
Link: https://doi.org/10.1016/..
 
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7

Elucidating the clinical spectrum and molecular basis of HY..:

Fasham, James ; Lin, Siying ; Ghosh, Promita...
Genetics in Medicine.  24 (2022)  3 - p. 631-644 , 2022
Link: https://doi.org/10.1016/..
 
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8

Clinical Validation of Genome Reference Consortium Human Bu..:

Lansdon, Lisa A ; Cadieux-Dion, Maxime ; Herriges, John C...
Clinical Chemistry.  68 (2022)  9 - p. 1177-1183 , 2022
Link: https://doi.org/10.1093/..
 
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9

Using dried blood spots for variant analysis for patients w..:

Amos, Lauren E. ; Yoo, Byunggil ; Miller, Neil...
Haemophilia.  25 (2019)  5 - p. , 2019
Link: https://doi.org/10.1111/..
 
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10

The NSIGHT1-randomized controlled trial: rapid whole-genome..:

Petrikin, Josh E. ; Cakici, Julie A. ; Clark, Michelle M....
npj Genomic Medicine.  3 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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11

Correction: Whole exome sequencing reveals HSPA1L as a gene..:

Huusko, Johanna M. ; Karjalainen, Minna K. ; Graham, Britney E....
PLOS Genetics.  14 (2018)  9 - p. e1007673 , 2018
Link: https://doi.org/10.1371/..
 
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12

Whole exome sequencing reveals HSPA1L as a genetic risk fac..:

Huusko, Johanna M. ; Karjalainen, Minna K. ; Graham, Britney E....
PLOS Genetics.  14 (2018)  7 - p. e1007394 , 2018
Link: https://doi.org/10.1371/..
 
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13

Erratum: Constellation: a tool for rapid, automated phenoty..:

Twist, Greyson P ; Gaedigk, Andrea ; Miller, Neil A...
npj Genomic Medicine.  2 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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14

In vivoCharacterization ofCYP2D6*12, *29and*84Using Dextrom..:

Gaedigk, Andrea ; Twist, Greyson P ; Farrow, Emily G...
Pharmacogenomics.  18 (2017)  5 - p. 427-431 , 2017
Link: https://doi.org/10.2217/..
 
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15

GPR37L1 modulates seizure susceptibility: Evidence from mou..:

Giddens, Michelle M. ; Wong, Jennifer C. ; Schroeder, Jason P....
Neurobiology of Disease.  106 (2017)  - p. 181-190 , 2017
Link: https://doi.org/10.1016/..
 
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