Mark D. Ludman - Concepedia

Author

Mark D. Ludman

Dalhousie University ORCID

Also Known As

M D Ludman, M Ludman, M. D. Ludman, M. Ludman, Mark D Ludman, Mark D. Ludman, Mark David Ludman, Mark Ludman

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

Dalhousie University Izaak Walton Killam Health Centre Université de Montréal Boston Children's Hospital University of British Columbia

About

Mark D. Ludman is an author at Dalhousie University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	1K
2	Health Sciences	1	1	40
3	Public Health	1	1	42
4	Social Sciences	1	1	36
5	Biostatistics	1	1	42

Mark D. Ludman

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia Duane L. Guernsey, Haiyan Jiang, Dean R. Campagna, Nature Genetics Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseHematology	2009	243
Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4 Duane L. Guernsey, Haiyan Jiang, Julie Hussin, The American Journal of Human Genetics Developmental BiologyCell DivisionMolecular GeneticsCentrosomal Protein Cep152Medicine	2010	194
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome Duane L. Guernsey, Makoto Matsuoka, Haiyan Jiang, Nature Genetics Allelic VariantMendelian DisorderGenetic DisorderGeneticsMolecular Genetics	2011	171
Overlapping spectra of <i>SMAD4</i> mutations in juvenile polyposis (JP) and JP–HHT syndrome Carol J. Gallione, Arthur S. Aylsworth, Jill Beis, American Journal of Medical Genetics Part A	2010	147
Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in theCOL1A1 andCOL1A2 genes of type I collagen Peter H. Byers, Madeleine Duvic, Mary Atkinson, American Journal of Medical Genetics	1997	126
Fabry disease: twenty-three mutations including sense and antisense CpG alterations and identification of a deletional hot-spot in the α-galactosidase A gene Christine M. Eng, Dana Niehaus, Annette L. Enriquez, Human Molecular Genetics	1994	115
Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2 Duane L. Guernsey, Haiyan Jiang, Susan C. Evans, The American Journal of Human Genetics GeneticsBiochemical GeneticsMolecular BiologyMolecular GeneticsGenomics	2009	92
Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease Duane L. Guernsey, Haiyan Jiang, Karen Bedard, PLoS Genetics	2010	69
Germline Mutations in MAP3K6 Are Associated with Familial Gastric Cancer Daniel Gaston, Samantha Hansford, Carla Oliveíra, PLoS Genetics OncologyGastrointestinal OncologyMedicineGeneticsMitogen-activated Protein Kinase	2014	66
Allogenic Bone Marrow Transplantation in Severe Gaucher Disease Philip H. Tsai, Jeffrey M. Lipton, Indira Sahdev, Pediatric Research TransplantationMarrow TransplantationSevere Gaucher DiseaseBone Marrow FailureStem Cell Transplantation	1992	64

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