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Sherr, Elliott H.
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1

Vasopressin deficiency: a hypothesized driver of both socia..:

Clarke, Lauren ; Gesundheit, Neil ; Sherr, Elliott H...
Molecular Psychiatry.  , 2024
Link: https://doi.org/10.1038/..
 
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2

The variant landscape and function of DDX3X in cancer and n..:

Gadek, Margaret ; Sherr, Elliott H. ; Floor, Stephen N.
Trends in Molecular Medicine.  29 (2023)  9 - p. 726-739 , 2023
Link: https://doi.org/10.1016/..
 
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3

TMTC4 is a hair cell–specific human deafness gene:

Li, Jiang ; Choi, Byung Yoon ; Eltawil, Yasmin...
JCI Insight.  8 (2023)  24 - p. , 2023
Link: https://doi.org/10.1172/..
 
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4

De novo CLCN3 variants affecting Gly327 cause severe neurod..:

Nakashima, Mitsuko ; Argilli, Emanuela ; Nakano, Sayaka...
Journal of Human Genetics.  68 (2022)  4 - p. 291-298 , 2022
Link: https://doi.org/10.1038/..
 
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5

Newborn screening for neurodevelopmental diseases: Are we t..:

Chung, Wendy K. ; Berg, Jonathan S. ; Botkin, Jeffrey R....
American Journal of Medical Genetics Part C: Seminars in Medical Genetics.  190 (2022)  2 - p. 222-230 , 2022
Link: https://doi.org/10.1002/..
 
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6

De Novo GLI3 Pathogenic Variants May Cause Hypotonia and a ..:

Siafa, Lyna ; Argilli, Emanuela ; Sherr, Elliott H..
Pediatric Neurology.  131 (2022)  - p. 1-3 , 2022
Link: https://doi.org/10.1016/..
 
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7

ANKLE2‐related microcephaly: A variable microcephaly syndro..:

Thomas, Ajay X. ; Link, Nichole ; Robak, Laurie A....
Annals of Clinical and Translational Neurology.  9 (2022)  8 - p. 1276-1288 , 2022
Link: https://doi.org/10.1002/..
 
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8

Systematic analysis and prediction of genes associated with..:

Leitão, Elsa ; Schröder, Christopher ; Parenti, Ilaria...
Nature Communications.  13 (2022)  1 - p. , 2022
Link: https://doi.org/10.1038/..
 
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9

Heterozygous variants in MYH10 associated with neurodevelop..:

Holtz, Alexander M. ; VanCoillie, Rachel ; Vansickle, Elizabeth A....
Genetics in Medicine.  24 (2022)  10 - p. 2065-2078 , 2022
Link: https://doi.org/10.1016/..
 
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10

DRAXIN regulates interhemispheric fissure remodelling to in..:

Morcom, Laura ; Edwards, Timothy J ; Rider, Eric...
eLife.  10 (2021)  - p. , 2021
Link: https://doi.org/10.7554/..
 
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11

Autism-associated biomarkers: test–retest reliability and r..:

Oztan, Ozge ; Talbot, Catherine F. ; Argilli, Emanuela...
Molecular Autism.  12 (2021)  1 - p. , 2021
Link: https://doi.org/10.1186/..
 
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12

Bi-allelic loss-of-function variants in BCAS3 cause a syndr..:

Hengel, Holger ; Hannan, Shabab B. ; Dyack, Sarah...
The American Journal of Human Genetics.  108 (2021)  6 - p. 1069-1082 , 2021
Link: https://doi.org/10.1016/..
 
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13

Whole-exome sequencing with targeted analysis and epilepsy ..:

Numis, Adam L. ; da Gente, Gilberto ; Sherr, Elliott H..
Pediatric Research.  91 (2021)  4 - p. 896-902 , 2021
Link: https://doi.org/10.1038/..
 
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14

DCC regulates astroglial development essential for telencep..:

Morcom, Laura ; Gobius, Ilan ; Marsh, Ashley PL...
eLife.  10 (2021)  - p. , 2021
Link: https://doi.org/10.7554/..
 
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15

William B. Dobyns:

, In: Child Neurology,
Sherr, Elliott H. - p. 696-698 , 2021
Link: https://doi.org/10.1016/..
 
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