Alexandra L. Joyner - Concepedia

Author

Alexandra L. Joyner

Also Known As

A JOYNER, A Joyner, A L Joyner, A. JOYNER, A. Joyner, A. L. Joyner, A.L. Joyner, A. L. Joyner, ALEXANDRA L. JOYNER, Alexandra Joyner

311

Publications

36.7K

Citations

H-Index

171

Concepts

All Affiliations

New York University Howard Hughes Medical Institute Kettering University University of Toronto Cornell University

About

Alexandra L. Joyner is an author at New York University specializing in medicine, developmental biology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	70	100	21.8K
2	Health Sciences	10	10	3.1K
3	Natural Sciences	7	7	1.4K
4	Engineering	4	4	2.9K
5	Public Health	1	1	258

Alexandra L. Joyner

160

Publications

31.4K

Citations

H-Index

Page 1

	Year	Citations
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes Shiaoching Gong, Zheng Chen, Martin L. Doughty, Nature EngineeringGeneticsComputational BiologyGene Expression AtlasSynthetic Biology	2003	2.1K
Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons François Guillemot, Liching Lo, Jane E. Johnson, Cell Developmental BiologyEarly DevelopmentAutonomic NeuronsPhysiologyIntercellular Communication	1993	1K
Glucose intolerance but normal satiety in mice with a null mutation in the glucagon–like peptide 1 receptor gene Louise A. Scrocchi, Theodore J. Brown, Neil J. MacLusky, Nature Medicine Metabolic SyndromeInsulin SignalingSignal TransductionG Protein-coupled ReceptorInsulin Management	1996	788
Inactivation of the Mouse Huntington's Disease Gene Homolog <i>Hdh</i> Mabel P. Duyao, Anna B. Auerbach, Angela Ryan, Science Knockout MouseNeurodegenerative DiseasesDevelopmental BiologyGenetic DisorderGenetics	1995	721
Mouse <i>Gli1</i> mutants are viable but have defects in SHH signaling in combination with a <i>Gli2</i> mutation H. L. Park, Chen Bai, Kenneth A. Platt, Development	2000	718
A mouse model of Greig cephalo–polysyndactyly syndrome: the extra–toesJ mutation contains an intragenic deletion of the Gli3 gene Chi‐chung Hui, Alexandra L. Joyner Nature Genetics Developmental BiologyMendelian DisorderGreig Cephalo–polysyndactyly SyndromeGenetic DisorderGenetics	1993	710
<i>Gli2</i>, but not<i>Gli1</i>, is required for initial Shh signaling and ectopic activation of the Shh pathway Chen Bai, Wojtek Auerbach, Joon S. Lee, Development Lineage PlasticityEctopic ActivationDevelopmental BiologySignal TransductionTissue Development	2002	696
In vivo analysis of quiescent adult neural stem cells responding to Sonic hedgehog Sohyun Ahn, Alexandra L. Joyner Nature Regenerative MedicineInduced Pluripotent Stem CellVivo AnalysisDevelopmental BiologyMedicine	2005	693
Targeted disruption of the trkB neurotrophin receptor gene results in nervous system lesions and neonatal death Rüdiger Klein, Richard J. Smeyne, Wolfgang Wurst, Cell NeuropeptidesNeonatal DeathNervous System LesionsCell DeathNeuropeptide Receptor	1993	671
The Knockout Mouse Project Christopher P. Austin, James F. Battey, Allan Bradley, Nature Genetics New TechnologiesEngineeringGene CharacterizationRobot LearningMultimodal Human Computer Interface	2004	614

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