C. McGraw

Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia

H. Zoghbi, Aya Ito-Ishida, R. Samaco, 2020, Frontiers in Neurology.

Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.

Rodney C. Samaco, H. Zoghbi, R. Samaco, 2013, Human molecular genetics.

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome

Rodney C. Samaco, C. Shaw, H. Zoghbi, 2011, Nature Genetics.

Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies

Rodney C. Samaco, R. Samaco, C. M. McGraw, 2017, American journal of medical genetics. Part C, Seminars in medical genetics.

Neurexophilin4 is a selectively expressed α-neurexin ligand that modulates specific cerebellar synapses and motor functions

H. Zoghbi, R. Sillitoe, Li Wang, 2019, eLife.

4 is A Selectively Expressed α-neurexin Ligand That Modulates Specific Cerebellar 1 Synapses and Motor Functions 2 3

H. Zoghbi, Wei Wang, Xiaolong Jiang, 2022 .

The locus encoding an oligomorphic family of MHC-A alleles (Mane-A*06/Mamu-A*05) is present at high frequency in several macaque species

V. Hirsch, A. Buckler-White, B. Lafont, 2007, Immunogenetics.

A 52-Year-Old Man With Seizures and Progressive Cerebrovascular Lesions

Sara C. LaHue, A. Bollen, M. Richie, 2020, The Neurohospitalist.

Adult Neural Function Requires MeCP2

Rodney C. Samaco, H. Zoghbi, R. Samaco, 2011, Science.

Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome

Jennie R. Green, Rodney C. Samaco, Agnes J. Liang, 2016, Human molecular genetics.