Matthijs J. Smith - Concepedia

Author

Matthijs J. Smith

Royal Children's Hospital

Also Known As

M J Smith, M SMITH, M.J. Smith, Matthijs J Smith, Matthijs J. Smith, Matthijs Smith

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital The University of Melbourne

About

Matthijs J. Smith is an author at Royal Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	3.7K
2	Natural Sciences	1	1	15
3	Public Health	1	1	68
4	Biology	1	1	15
5	Child Development	1	1	204

Matthijs J. Smith

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif Andrew Sinclair, Philippe Berta, Mark S. Palmer, Nature ChromatinSex DeterminationDna-binding MotifGeneticsSex Differences	1990	3.2K
National cancer clinical trials: Children have equal access; adolescents do not W. Archie Bleyer, Heriberto A. Tejeda, Sabina A. Murphy, Journal of Adolescent Health Family MedicineAdolescent MedicineMedicinePediatricsEqual Access	1997	204
Gene expression during gonadogenesis in the chicken embryo Craig A. Smith, Matthijs J. Smith, Andrew Sinclair Gene Developmental BiologyGeneticsMorphogenesisEmbryonic DevelopmentReproductive Biology	1999	135
ASW: a gene with conserved avian W-linkage and female specific expression in chick embryonic gonad Michael J. O’Neill, Michele D. Binder, Craig A. Smith, Development Genes and Evolution	2000	130
Expression of Chicken Steroidogenic Factor-1 during Gonadal Sex Differentiation Craig A. Smith, Matthijs J. Smith, Andrew Sinclair General and Comparative Endocrinology Developmental BiologyFertilityChicken Steroidogenic Factor-1Reproductive BiologyPublic Health	1999	68
SOX14 is a candidate gene for limb defects associated with BPES and M�bius syndrome Helen P. Wilmore, Matthijs J. Smith, S.A. Wilcox, Human Genetics Limb DefectsMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2000	20
Familial Kallmann syndrome: a novel splice acceptor mutation in the KAL gene. M J O'Neill, Bambang Tridjaja, Matthijs J. Smith, PubMed Developmental BiologyMendelian DisorderKal GeneGenetic DisorderGenetics	1998	20
MIC2R: a transcribed <i>MIC2</i>-related sequence associated with a CpG island in the human pseudoautosomal region Matthijs J. Smith, Peter N. Goodfellow Human Molecular Genetics GeneticsPathologyMolecular GeneticsGenomicsSplicing Variant	1994	15

Page 1