Heather L. Hinds - Concepedia

Concepedia

Author

Heather L. Hinds

University of Oxford

Also Known As

H Hinds, H L Hinds, H. Hinds, Heather Hinds, Heather L. Hinds

15

Publications

1.1K

Citations

9

H-Index

41

Concepts

All Affiliations

University of Oxford Massachusetts Institute of Technology Howard Hughes Medical Institute

HL

About

Heather L. Hinds is an author at University of Oxford specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	918
2	Cell Biology	2	2	478
3	Health Sciences	1	1	93
4	Social Sciences	1	1	88
5	Cellular Physiology	1	1	88

Heather L. Hinds

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9

Publications

1.1K

Citations

9

H-Index

	Year	Citations
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndrome Heather L. Hinds, Claude T. Ashley, James S. Sutcliffe, Nature Genetics Fragile X SyndromeDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1993	390
Motoneuron-Specific Expression of NR3B, a Novel NMDA-Type Glutamate Receptor Subunit That Works in a Dominant-Negative Manner Mayumi Nishi, Heather L. Hinds, Haiping Lu, Journal of Neuroscience Signal TransductionMolecular PhysiologySynaptic TransmissionNeurotransmitterMotoneuron-specific Expression	2001	254
Clonal analysis of human tumors with M27 beta, a highly informative polymorphic X chromosomal probe. Martin F. Fey, H J Peter, Heather L. Hinds, Journal of Clinical Investigation GeneticsHuman PolymorphismPathologyEpigeneticsTumor Biology	1992	93
Essential function of α-calcium/calmodulin-dependent protein kinase II in neurotransmitter release at a glutamatergic central synapse Heather L. Hinds, Ivan Goussakov, Kazu Nakazawa, Proceedings of the National Academy of Sciences	2003	93
CA1 Long-Term Potentiation Is Diminished but Present in Hippocampal Slices from α-CaMKII Mutant Mice Heather L. Hinds, Susumu Tonegawa, Roberto Malinow Learning & Memory Synaptic TransmissionGeneticsLtp DeficitNeurotransmissionCellular Neurobiology	1998	88
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motif Heather L. Hinds, Rudi W. Hendriks, Ian Craig, Genomics Genetic DisorderGeneticsHuman PolymorphismMolecular BiologyPolymorphic Region	1992	69
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the Monoamine Oxidase A gene Rudi W. Hendriks, Z Y Chen, Heather L. Hinds, Human Molecular Genetics	1992	52
An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene Rudi W. Hendriks, Zhengyi Chen, Heather L. Hinds, Human Molecular Genetics	1992	36
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosome Rudi W. Hendriks, Heather L. Hinds, Zhengyi Chen, Genomics ChromatinCpg IslandGenetic DisorderEpigenetic ChangeGenetics	1992	24

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