Jillian M. Felie - Concepedia

Concepedia

Author

Jillian M. Felie

Howard Hughes Medical Institute

Also Known As

J.M. Felie, Jillian Felie, Jillian M Felie, Jillian M. Felie, Jillian M. Felie

10

Publications

1.3K

Citations

8

H-Index

29

Concepts

All Affiliations

Howard Hughes Medical Institute Harvard University Massachusetts General Hospital Massachusetts Institute of Technology Boston Children's Hospital

JM

About

Jillian M. Felie is an author at Howard Hughes Medical Institute specializing in medicine, genetics, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	805
2	Natural Sciences	2	2	97
3	Cell Biology	2	2	207
4	Health Sciences	1	1	282
5	Biochemistry	1	1	47

Jillian M. Felie

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8

Publications

1.3K

Citations

8

H-Index

	Year	Citations
Using Whole-Exome Sequencing to Identify Inherited Causes of Autism Timothy W. Yu, Maria H. Chahrour, Michael E. Coulter, Neuron Whole-exome SequencingGeneticsSyndromic AutismAutism	2013	456
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture Timothy W. Yu, Ganeshwaran H. Mochida, David J. Tischfield, Nature Genetics Centrosome-associated ProteinDevelopmental BiologyBrain StructureBrain DevelopmentNeuroanatomy	2010	282
Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly Fowzan S. Alkuraya, Xuyu Cai, Carina Emery, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsDisease Gene Identification	2011	219
A Homozygous Mutation in the Tight-Junction Protein JAM3 Causes Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Congenital Cataracts Ganeshwaran H. Mochida, Vijay Ganesh, Jillian M. Felie, The American Journal of Human Genetics OphthalmologyGenetic DisorderMedicineHomozygous MutationSubependymal Calcification	2010	104
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development Ganeshwaran H. Mochida, Vijay Ganesh, María I. de Michelena, Nature Genetics Signal TransductionDevelopmental BiologySynaptic SignalingMolecular RegulationGenetics	2012	103
METTL23, a transcriptional partner of GABPA, is essential for human cognition Rachel E. Reiff, Bassam R. Ali, Byron Baron, Human Molecular Genetics Transcriptional RegulationSystems BiologyGenetic DisorderArab OriginGenetics	2014	50
Expression and localization of Na-driven Cl-HCO3− exchanger (SLC4A8) in rodent CNS Liming Chen, M.L. Kelly, Michael D. Parker, Neuroscience Molecular NeuroscienceSignal TransductionBiochemistryMolecular PhysiologyNa-driven Cl-hco3− Exchanger	2008	47
Phenotypic heterogeneity in Woodhouse–Sakati syndrome: Two new families with a mutation in the C2orf37 gene Tawfeg Ben‐Omran, Rehab Ali, Mariam Al‐Mureikhi, American Journal of Medical Genetics Part A	2011	34

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