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Author Details
Full Name
Sarah E Marsh
Affiliation
University of Wisconsin
ORCID
Career Start Year
2003
Papers
15
H Index
13
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
25058579
Interaction between workers during a short time window is required for bacterial symbiont transmission in Acromyrmex leaf-cutting ants.
PLoS One
2014
24151778
Association between Pseudonocardia symbionts and Atta leaf-cutting ants suggested by improved isolation methods.
Int Microbiol
2013
22246503
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium.
Nat Genet
2012
21263138
Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families.
Neurology
2011
21347285
The genome sequence of the leaf-cutter ant Atta cephalotes reveals insights into its obligate symbiotic lifestyle.
PLoS Genet
2011
18268248
The molar tooth sign: a new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families.
Neurology
2008
18674751
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.
Am J Hum Genet
2008
17564967
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Am J Hum Genet
2007
16453322
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders.
Ann Neurol
2006
15786477
Distinguishing the four genetic causes of Jouberts syndrome-related disorders.
Ann Neurol
2005
15119486
Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.
J Child Neurol
2004
15467982
Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria.
Am J Hum Genet
2004
14981712
Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.
Am J Med Genet A
2004
14684696
Patient with bilateral periventricular nodular heterotopia and polymicrogyria with apparently balanced reciprocal translocation t(1;6)(p12;p12.2) that interrupts the mannosidase alpha, class 1A, and glutathione S-transferase A2 genes.
J Med Genet
2003
12917796
Linkage analysis in families with Joubert syndrome plus oculo-renal involvement identifies the CORS2 locus on chromosome 11p12-q13.3.
Am J Hum Genet
2003
1 - 15 of 15
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