Takuya Fujiwara - Concepedia

Author

Takuya Fujiwara

Also Known As

Fujiwara, T, T FUJIWARA, T Fujiwara, T M Fujiwara, T Mary Fujiwara, T. FUJIWARA, T. Fujiwara, T. M. Fujiwara, T. MARY FUJIWARA, T. Mary Fujiwara

198

Publications

Citations

H-Index

183

Concepts

All Affiliations

McGill University McGill University Health Centre University of Manitoba Iwate Medical University Montreal General Hospital

About

Takuya Fujiwara is an author at McGill University specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	28	40	4.5K
2	Health Sciences	8	8	1.5K
3	Engineering	3	3	83
4	Language Studies	1	1	19
5	Natural Sciences	1	1	34

Takuya Fujiwara

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Troglitazone increases the number of small adipocytes without the change of white adipose tissue mass in obese Zucker rats. Akira Okuno, Hiroyuki Tamemoto, Kazuuki TOBE, Journal of Clinical Investigation Metabolic DisorderMetabolic RemodelingInsulin SignalingObesityMetabolic Syndrome	1998	997
SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaPi-IIc in Maintaining Phosphate Homeostasis Clemens Bergwitz, Nicole M. Roslin, Martin Tieder, The American Journal of Human Genetics Slc34a3 MutationsUrologyMolecular PhysiologySodium HomeostasisGenetic Disorder	2006	479
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type Jordan Lerner‐Ellis, Jamie C. Tirone, Peter D. Pawelek, Nature Genetics BiologyCblc TypeMethylmalonic AciduriaGenetic DisorderGenetics	2005	372
Limb-Girdle Muscular Dystrophy Type 2H Associated with Mutation in TRIM32, a Putative E3-Ubiquitin–Ligase Gene Patrick Frosk, Tracey Weiler, Edward Nylen, The American Journal of Human Genetics Putative E3-ubiquitin–ligase GeneMendelian DisorderGenetic DisorderGeneticsMolecular Genetics	2002	255
Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification Kym M. Boycott, Shauna Flavelle, Alexandre Bureau, The American Journal of Human Genetics Homozygous DeletionNeurodegenerative DiseasesMendelian DisorderGenetic DisorderGenetics	2005	216
Linkage of Tuberculosis to Chromosome 2q35 Loci, Including NRAMP1, in a Large Aboriginal Canadian Family Celia M.T. Greenwood, Takuya Fujiwara, Lucy J. Boothroyd, The American Journal of Human Genetics Including Nramp1Pulmonary TuberculosisGeneticsGenetic EpidemiologyPathology	2000	203
Report of 33 Novel AVPR2 Mutations and Analysis of 117 Families with X-Linked Nephrogenic Diabetes Insipidus Marie-FrancCOMBINING CEDILLAoise Arthus, MICHECombining Grave AccentLE LONERGAN, M. JOYCE CRUMLEY, Journal of the American Society of Nephrology	2000	185
Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. Jie Liu, Takuya Fujiwara, Natalie Buu, PubMed	1995	172
Characterization of new oral antidiabetic agent CS-045. Studies in KK and ob/ob mice and Zucker fatty rats Takuya Fujiwara, S. Yoshioka, Tomohisa Yoshioka, Diabetes InflammationMetabolic SyndromeDiabetes ManagementInsulin ManagementPhysiology	1988	158
X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis. Daniel G. Bichet, Marie‐Françoise Arthus, Michèle Lonergan, Journal of Clinical Investigation GeneticsGenetic EpidemiologyHuman PolymorphismPathologyMolecular Genetics	1993	151

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