H. Zoghbi
Molecular Biology · 2000–2012
A researcher in the Science corpus: 14 papers; trusts 17 researchers and is trusted by 35 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 161 citations into it; #5,298 of 17,773 by trust here, #1,583 by citations
- Genetics — 91 citations into it; #449 of 6,854 by trust here, #591 by citations
- Cognitive Neuroscience — 60 citations into it; #1,317 of 10,852 by trust here, #1,681 by citations
- Cellular and Molecular Neuroscience — 56 citations into it; #1,371 of 2,998 by trust here, #579 by citations
- Cell Biology — 19 citations into it
- Physiology — 7 citations into it
Whom H. Zoghbi trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- A. Bird
- Mark F. Bear
- C. Betancur
- T. Sūdhof
- T. Bale
- J. Gan
- R. Jaenisch
- K. Huber
- M. Missler
- Maria H. Chahrour
Who trusts H. Zoghbi overall
- Alexander A. Chubykin
- Daniel H. Geschwind
- C. Kwon
- Thomas Bourgeron
- Geraldine Dawson
- R. J. Kelleher
- Paul L. Greer
- D. Selkoe
- Richard I. Morimoto
- Claudio Soto
Papers from H. Zoghbi's perspective
Ordered by how strongly the researchers H. Zoghbi trusts endorse each paper. Same corpus, a different order for every researcher.
- DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation (Science)
- Neurexins induce differentiation of GABA and glutamate postsynaptic specializations via neuroligins. (Cell)
- X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family. (American Journal of Human Genetics)
- MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription (Science)
- Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice (Nature Genetics)
- Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting. (Brain Research)
- Altered synaptic plasticity in a mouse model of fragile X mental retardation (Proceedings of the National Academy of Sciences of the United States of America)
- Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders (Nature Genetics)
- Neuroligins determine synapse maturation and function. (Neuron)
- The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation* (Journal of Biological Chemistry)
Their papers
- Towards a proteome-scale map of the human protein–protein interaction network (2005) — 3,029 citations
- Glutamine repeats and neurodegeneration. (2000) — 1,304 citations
- Identification of genes that modify ataxin-1-induced neurodegeneration (2000) — 684 citations
- Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. (2002) — 794 citations
- Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. (2004) — 644 citations
- The DNA sequence of the human X chromosome (2005) — 1,099 citations
- The story of Rett syndrome: from clinic to neurobiology. (2007) — 1,290 citations
- Diseases of Unstable Repeat Expansion: Mechanisms and Common Principles (2005) — 794 citations
- Trinucleotide repeat disorders. (2007) — 1,445 citations
- Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities. (2012) — 770 citations
- GABAergic dysfunction mediates autism-like stereotypies and Rett syndrome phenotypes (2010) — 710 citations
- MeCP2, a Key Contributor to Neurological Disease, Activates and Represses Transcription (2008) — 1,838 citations
- Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (2003) — 709 citations
- Requirement of Math1 for Secretory Cell Lineage Commitment in the Mouse Intestine (2001) — 976 citations