David Markie - Concepedia

Author

David Markie

Also Known As

D M Markie, D Markie, D. MARKIE, D. Markie, D.M. Markie, David M Markie, David M. Markie, David Markie, David M. Markie, Markie, David M.

Publications

6.5K

Citations

H-Index

Concepts

All Affiliations

University of Otago The Honourable Society of Lincoln's Inn Dunedin Public Hospital Children's Hospital at Westmead The Ohio State University

About

David Markie is an author at University of Otago specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	23	31	4.1K
2	Natural Sciences	3	3	146
3	Engineering	2	2	68
4	Public Health	2	2	111
5	Health Sciences	1	1	19

David Markie

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome Akseli Hemminki, David Markie, Ian Tomlinson, Nature Genetic DisorderMedicineGeneticsSerine/threonine Kinase GeneDisease Gene Identification	1998	1.6K
Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis Eugene D. Carstea, Jill A. Morris, Katherine Coleman, Science	1997	1.5K
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis Akseli Hemminki, Ian Tomlinson, David Markie, Nature Genetics Genetic DisorderGeneticsComparative Genomic HybridizationLinkage AnalysisPathology	1997	493
Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development Silvia Cappello, Mary Jane Gray, Caroline Badouel, Nature Genetics Molecular NeuroscienceDevelopmental BiologySignaling PathwayBrain DevelopmentCerebral Cortical Development	2013	276
Germline Mutations in BMPR1A/ALK3 Cause a Subset of Cases of Juvenile Polyposis Syndrome and of Cowden and Bannayan-Riley-Ruvalcaba Syndromes* Xiaoping Zhou, K Woodford-Richens, Rainer Lehtonen, The American Journal of Human Genetics Genetic DisorderGeneticsPathogenesisPathologyJuvenile Polyposis Syndrome	2001	257
Mutations in PYCR1 cause cutis laxa with progeroid features Bruno Reversade, Nathalie Escande‐Beillard, Aikaterini Dimopoulou, Nature Genetics BiologyPlant BiologyGeneticsPathogenesisPlant Pathology	2009	252
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases Richard S. Houlston, Steve Bevan, Alison C. Williams, Human Molecular Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsPathogenesis	1998	144
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis K Woodford-Richens, Steve Bevan, Michael Churchman, Gut	2000	134
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Nature Communications	2017	106
Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. Sylviane Olschwang, David Markie, S. Seal, Journal of Medical Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	1998	101

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