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Chahrour, Maria H.
95  Ergebnisse:
Personensuche X
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1

The genetics of autism spectrum disorder in an East African..:

Tuncay, Islam Oguz ; DeVries, Darlene ; Gogate, Ashlesha...
Cell Genomics.  3 (2023)  7 - p. 100322 , 2023
Link: https://doi.org/10.1016/..
 
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2

RAB1A haploinsufficiency phenocopies the 2p14–p15 microdele..:

Rios, Jonathan J. ; Li, Yang ; Paria, Nandina...
The American Journal of Human Genetics.  110 (2023)  12 - p. 2103-2111 , 2023
Link: https://doi.org/10.1016/..
 
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3

Genomic strategies to untangle the etiology of autism: A pr..:

Vashisth, Shayal ; Chahrour, Maria H.
Autism Research.  16 (2022)  1 - p. 31-39 , 2022
Link: https://doi.org/10.1002/..
 
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4

Analysis of recent shared ancestry in a familial cohort ide..:

Tuncay, Islam Oguz ; Parmalee, Nancy L. ; Khalil, Raida...
npj Genomic Medicine.  7 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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5

Insights Into DDX3X Syndrome From a Novel Mouse Model With ..:

Vashisth, Shayal ; Chahrour, Maria H.
Biological Psychiatry.  90 (2021)  11 - p. 732-734 , 2021
Link: https://doi.org/10.1016/..
 
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6

Homozygous deletions implicate non-coding epigenetic marks ..:

Schmitz-Abe, Klaus ; Sanchez-Schmitz, Guzman ; Doan, Ryan N....
Scientific Reports.  10 (2020)  1 - p. , 2020
Link: https://doi.org/10.1038/..
 
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7

KDM5A mutations identified in autism spectrum disorder usin..:

El Hayek, Lauretta ; Tuncay, Islam Oguz ; Nijem, Nadine...
eLife.  9 (2020)  - p. , 2020
Link: https://doi.org/10.7554/..
 
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8

The ubiquitin ligase UBE3B, disrupted in intellectual disab..:

Cheon, Solmi ; Kaur, Kiran ; Nijem, Nadine...
Proceedings of the National Academy of Sciences.  116 (2019)  9 - p. 3662-3667 , 2019
Link: https://doi.org/10.1073/..
 
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9

The ubiquitin ligase UBE3B, disrupted in intellectual disab..:

Cheon, Solmi ; Kaur, Kiran ; Nijem, Nadine...
Proceedings of the National Academy of Sciences of the United States of America.  116 (2019)  9 - p. 3662-3667 , 2019
Link: https://www.jstor.org/st..
 
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10

PSMD12 haploinsufficiency in a neurodevelopmental disorder ..:

Khalil, Raida ; Kenny, Connor ; Hill, R. Sean...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.  177 (2018)  8 - p. 736-745 , 2018
Link: https://doi.org/10.1002/..
 
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11

Variability of Ponto-cerebellar Fibers by Diffusion Tensor ..:

Rollins, Nancy K. ; Booth, Timothy N. ; Chahrour, Maria H.
Journal of Child Neurology.  32 (2016)  3 - p. 271-285 , 2016
Link: https://doi.org/10.1177/..
 
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12

MeCP2 and histone deacetylases 1 and 2 in dorsal striatum c..:

Mahgoub, Melissa ; Adachi, Megumi ; Suzuki, Kanzo...
Nature Neuroscience.  19 (2016)  11 - p. 1506-1512 , 2016
Link: https://doi.org/10.1038/..
 
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13

Rett-causing mutations reveal two domains critical for MeCP..:

Heckman, Laura Dean ; Chahrour, Maria H ; Zoghbi, Huda Y
eLife.  3 (2014)  - p. , 2014
Link: https://doi.org/10.7554/..
 
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14

Synaptic, transcriptional and chromatin genes disrupted in ..:

The DDD Study ; De Rubeis, Silvia ; He, Xin...
Nature.  515 (2014)  7526 - p. 209-215 , 2014
Link: https://doi.org/10.1038/..
 
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15

The Diverse Genetic Landscape of Neurodevelopmental Disorde..:

Hu, Wen F. ; Chahrour, Maria H. ; Walsh, Christopher A.
Annual Review of Genomics and Human Genetics.  15 (2014)  1 - p. 195-213 , 2014
Link: https://doi.org/10.1146/..
 
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