S. E. Marsh

发表

The Genome Sequence of the Leaf-Cutter Ant Atta cephalotes Reveals Insights into Its Obligate Symbiotic Lifestyle

Brian R. Johnson, Erich Bornberg-Bauer, Steven C. Slater, 2011, PLoS genetics.

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. Wheless, D. Pilz, W. Dobyns, 2003, Journal of medical genetics.

The molar tooth sign

M. Ross, A. Barkovich, W. Dobyns, 2008, Neurology.

A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families

M. Ross, W. Dobyns, J. Gleeson, 2008 .

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families

C. Truwit, N. Chuang, H. Kayserili, 2011, Neurology.

CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.

E. Bertini, R. Hennekam, H. Kayserili, 2007, American journal of human genetics.

Distinguishing the four genetic causes of jouberts syndrome–related disorders

E. Bertini, M. Koenig, H. Kayserili, 2005, Annals of neurology.

Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria.

H. Kayserili, J. Gleeson, L. Al-Gazali, 2004, American journal of human genetics.

AHI1 gene mutations cause specific forms of Joubert syndrome–related disorders

E. Bertini, F. Brancati, E. Valente, 2006, Annals of neurology.

Morphometric Analyses of Ears in Two Familes of Pinnipeds

S. E. Marsh, 2001 .

Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome.

Colin A. Johnson, I. Glass, F. Brancati, 2008, American journal of human genetics.

Social recognition using chemical cues in cuttlefish (Sepia officinalis Linnaeus, 1758)

J. Boal, S. E. Marsh, 1998 .

Molar tooth sign of the midbrain–hindbrain junction: Occurrence in multiple distinct syndromes

I. Glass, A. Barkovich, W. Dobyns, 2004, American journal of medical genetics. Part A.

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

Colin A. Johnson, S. Nelson, B. Merriman, 2011, Nature Genetics.

Linkage analysis in families with Joubert syndrome plus oculo-renal involvement identifies the CORS2 locus on chromosome 11p12-q13.3.

C. Woods, J. Gleeson, L. Al-Gazali, 2003, American journal of human genetics.

Association between Pseudonocardia symbionts and Atta leaf-cutting ants suggested by improved isolation methods.

M. Poulsen, C. Currie, A. Pinto-Tomás, 2013, International microbiology : the official journal of the Spanish Society for Microbiology.

Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts.

A. Barkovich, J. Gleeson, P. Grattan-Smith, 2004, Journal of Child Neurology.

Interaction between Workers during a Short Time Window Is Required for Bacterial Symbiont Transmission in Acromyrmex Leaf-Cutting Ants

M. Poulsen, C. Currie, A. Pinto-Tomás, 2014, PloS one.