Anna Lehman - Concepedia

Author

Anna Lehman

Also Known As

A. Lehman, A. M. Lehman, A., Lehman, A.M. Lehman, AM Lehman, Allison M B Lehman, Anna Lehman, Anna M Lehman, Anna M. Lehman, Anna M. Lehman

171

Publications

4.7K

Citations

H-Index

105

Concepts

All Affiliations

University of British Columbia BC Children's Hospital Child and Family Research Institute University of Toronto Children's & Women's Health Centre of British Columbia

About

Anna Lehman is an author at University of British Columbia specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	30	2.2K
2	Natural Sciences	2	2	322
3	Education	1	1	15
4	Engineering	1	1	50
5	Health Sciences	1	1	54

Anna Lehman

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
Exome Sequencing and the Management of Neurometabolic Disorders Maja Tarailo‐Graovac, Casper Shyr, Colin J.D. Ross, New England Journal of Medicine	2016	274
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders Víctor Faúndes, William G. Newman, Laura Bernardini, The American Journal of Human Genetics Histone ModificationsChromatinDevelopmental BiologyHistone Lysine MethylasesChromatin Remodeling	2017	268
Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans Jan Halbritter, Albane A. Bizet, Miriam Schmidts, The American Journal of Human Genetics	2013	225
Transcriptional Regulation of BACE1, the β-Amyloid Precursor Protein β-Secretase, by Sp1 Michelle A. Christensen, Weihui Zhou, Hong Qing, Molecular and Cellular Biology Transcriptional RegulationSystems BiologyProtein FunctionProtein ExpressionProtein Secretion	2003	220
Mutations in NOTCH1 Cause Adams-Oliver Syndrome Anna-Barbara Stittrich, Anna Lehman, Dale L. Bodian, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyGenetic DisorderGeneticsPathogenesis	2014	185
Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis Gaurav V. Harlalka, Anna Lehman, Barry A. Chioza, Brain GeneticsGlycobiologyMolecular BiologyMolecular GeneticsComplex Ganglioside Biosynthesis	2013	139
Loss-of-Function and Gain-of-Function Mutations in KCNQ5 Cause Intellectual Disability or Epileptic Encephalopathy Anna Lehman, Samrat Thouta, Grazia M.S. Mancini, The American Journal of Human Genetics Epileptic EncephalopathyNeurophysiologyGenetic DisorderGeneticsGain-of-function Mutations	2017	124
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly Diana Alcantara, Andrew E. Timms, Karen W. Gripp, Brain	2017	110
Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis James T. Bennett, Tiong Yang Tan, Diana Alcantara, The American Journal of Human Genetics PathologyFibroblast Growth FactorMolecular PathologyMosaic Activating MutationsCancer Genetics	2016	105
Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood Clara D.M. van Karnebeek, William S. Sly, Colin J.D. Ross, The American Journal of Human Genetics	2014	104

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