Kerry A. Miller - Concepedia

Concepedia

Author

Kerry A. Miller

Murdoch Children's Research Institute ORCID

Also Known As

K A Miller, K. A. Miller, Kerry A Miller, Kerry A. Miller, Kerry Ann Miller, Kerry A. Miller

37

Publications

1.6K

Citations

17

H-Index

48

Concepts

All Affiliations

Murdoch Children's Research Institute University of Oxford The University of Melbourne Royal Children's Hospital Victorian Clinical Genetics Services

KA

About

Kerry A. Miller is an author at Murdoch Children's Research Institute specializing in medicine, developmental biology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	897
2	Cell Biology	6	6	267
3	Social Sciences	2	2	41
4	Health Sciences	1	1	28
5	Biochemistry	1	1	158

Kerry A. Miller

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25

Publications

1.6K

Citations

17

H-Index

	Year	Citations
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders Jenny C. Taylor, Hilary C. Martin, Stefano Lise, Nature Genetics SequencingPsychiatryClinical GenomeGeneticsMedicine	2015	378
A biallelic mutation in <i>IL6ST</i> encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis Tobias Schwerd, Stephen R.F. Twigg, Dominik Aschenbrenner, The Journal of Experimental Medicine	2017	193
A new formula for a half-oxidized hematoxylin solution that neither overstains nor requires differentiation. Gary W. Gill, J K Frost, Kerry A. Miller PubMed BiochemistryMedicineHeme DegradationNew FormulaHematology	1974	158
Diagnostic value of exome and whole genome sequencing in craniosynostosis Kerry A. Miller, Stephen R.F. Twigg, Simon J. McGowan, Journal of Medical Genetics	2016	120
Mutations in CDC45 , Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis Aimée L Fenwick, Maciej Kliszczak, Fay Cooper, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsPre-initiation Complex	2016	116
A Recurrent Mosaic Mutation in SMO , Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones Syndrome Stephen R.F. Twigg, Robert B. Hufnagel, Kerry A. Miller, The American Journal of Human Genetics	2016	91
Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability Stephen R.F. Twigg, Jennifer Forecki, Jacqueline A.C. Goos, The American Journal of Human Genetics	2015	79
Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome Kerry A. Miller, Casey Ah-Cann, Megan F. Welfare, PLoS Genetics GeneticsPathologyDisease Gene IdentificationDigit AnomaliesTissue Development	2013	63
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder Margot R.F. Reijnders, Kerry A. Miller, Mohsan Alvi, The American Journal of Human Genetics	2018	48
A Mutation in Synaptojanin 2 Causes Progressive Hearing Loss in the ENU-Mutagenised Mouse Strain Mozart Shehnaaz S.M. Manji, Louise H. Williams, Kerry A. Miller, PLoS ONE	2011	45

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