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Ruzzo, Elizabeth
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1

INHERITED AND DE NOVO GENETIC RISK FOR AUTISM IMPACTS SHARE..:

Ruzzo, Elizabeth ; Perez-Cano, Laura ; Jung, Jae-Yoon...
European Neuropsychopharmacology.  29 (2019)  - p. S35-S36 , 2019
Link: https://doi.org/10.1016/..
 
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2

The contributions of rare inherited and polygenic risk to A..:

Cirnigliaro, Matilde ; Chang, Timothy S. ; Arteaga, Stephanie A....
Proceedings of the National Academy of Sciences.  120 (2023)  31 - p. , 2023
Link: https://doi.org/10.1073/..
 
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3

Noncoding deletions reveal a gene that is critical for inte..:

Oz-Levi, Danit ; Olender, Tsviya ; Bar-Joseph, Ifat...
Nature.  571 (2019)  7763 - p. 107-111 , 2019
Link: https://doi.org/10.1038/..
 
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4

Inherited and De Novo Genetic Risk for Autism Impacts Share..:

Ruzzo, Elizabeth K. ; Pérez-Cano, Laura ; Jung, Jae-Yoon...
Cell.  178 (2019)  4 - p. 850-866.e26 , 2019
Link: https://doi.org/10.1016/..
 
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5

A Single-Cell Transcriptomic Atlas of Human Neocortical Dev..:

Polioudakis, Damon ; de la Torre-Ubieta, Luis ; Langerman, Justin...
Neuron.  103 (2019)  5 - p. 785-801.e8 , 2019
Link: https://doi.org/10.1016/..
 
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6

Genetic epilepsy with febrile seizures plus: Refining the s..:

Zhang, Yue-Hua ; Burgess, Rosemary ; Malone, Jodie P....
Neurology.  89 (2017)  12 - p. 1210-1219 , 2017
Link: https://doi.org/10.1212/..
 
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7

TECPR2 mutations cause a new subtype of familial dysautonom..:

Heimer, Gali ; Oz-Levi, Danit ; Eyal, Eran...
European Journal of Paediatric Neurology.  20 (2016)  1 - p. 69-79 , 2016
Link: https://doi.org/10.1016/..
 
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8

Schizophrenia genetics complements its mechanistic understa..:

Ruzzo, Elizabeth K ; Geschwind, Daniel H
Nature Neuroscience.  19 (2016)  4 - p. 523-525 , 2016
Link: https://doi.org/10.1038/..
 
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9

Copy number variant analysis from exome data in 349 patient..:

Epilepsy Phenome/Genome Project & Epi4K Consortium ; Allen, Andrew S. ; Berkovic, Samuel F....
Annals of Neurology.  78 (2015)  2 - p. 323-328 , 2015
Link: https://doi.org/10.1002/..
 
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10

Whole-exome sequencing in undiagnosed genetic diseases: int..:

Zhu, Xiaolin ; Petrovski, Slavé ; Xie, Pingxing...
Genetics in Medicine.  17 (2015)  10 - p. 774-781 , 2015
Link: https://doi.org/10.1038/..
 
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11

Deficiency of Asparagine Synthetase Causes Congenital Micro..:

Ruzzo, Elizabeth K. ; Capo-Chichi, José-Mario ; Ben-Zeev, Bruria...
Neuron.  80 (2013)  2 - p. 429-441 , 2013
Link: https://doi.org/10.1016/..
 
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12

Exome Sequencing Followed by Large-Scale Genotyping Fails t..:

Heinzen, Erin L. ; Depondt, Chantal ; Cavalleri, Gianpiero L....
The American Journal of Human Genetics.  91 (2012)  2 - p. 293-302 , 2012
Link: https://doi.org/10.1016/..
 
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13

Using ERDS to Infer Copy-Number Variants in High-Coverage G..:

Zhu, Mingfu ; Need, Anna C. ; Han, Yujun...
The American Journal of Human Genetics.  91 (2012)  3 - p. 408-421 , 2012
Link: https://doi.org/10.1016/..
 
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14

SVA: software for annotating and visualizing sequenced huma..:

Ge, Dongliang ; Ruzzo, Elizabeth K. ; Shianna, Kevin V....
Bioinformatics.  27 (2011)  14 - p. 1998-2000 , 2011
Link: https://doi.org/10.1093/..
 
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15

The Characterization of Twenty Sequenced Human Genomes:

Pelak, Kimberly ; Shianna, Kevin V. ; Ge, Dongliang...
PLoS Genetics.  6 (2010)  9 - p. e1001111 , 2010
Link: https://doi.org/10.1371/..
 
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