J. Vesa - Concepedia

Author

J. Vesa

Institute for Molecular Medicine Finland

Also Known As

H. Harno, J Vesa, J. (a) Vesa, J. Vesa, Jouni Vesa

Publications

664

Citations

H-Index

Concepts

All Affiliations

Institute for Molecular Medicine Finland University of Helsinki University of British Columbia The University of Tokyo Karolinska University Hospital

About

J. Vesa is an author at Institute for Molecular Medicine Finland specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	130
2	Natural Sciences	1	1	183
3	Public Health	1	1	16
4	Social Sciences	1	1	20
5	Biochemistry	1	1	183

J. Vesa

Publications

626

Citations

H-Index

Page 1

	Year	Citations
DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence Ferdinando Squitieri, Susan E. Andrew, Y. Paul Goldberg, Human Molecular Genetics	1994	183
Human palmitoyl protein thioesterase: evidence for lysosomal targeting of the enzyme and disturbed cellular routing in infantile neuronal ceroid lipofuscinosis. Elina Hellsten, J. Vesa, Vesa M. Olkkonen, The EMBO Journal Lipid SynthesisBiochemistryLysosomal TargetingNatural SciencesLipid Science	1996	183
Ancestral differences in the distribution of the Δ2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease E. Almqvist, Niamh Spence, K. Nichol, Human Molecular Genetics	1995	68
An <i>Alu</i> variable polyA repeat polymorphism upstream of L-<i>myc</i> at 1p32 Tomi P. Mäkelä, Elina Hellsten, J. Vesa, Human Molecular Genetics Helsinki00290 Helsinki SearchGeneticsGenetic EpidemiologyHuman PolymorphismPathology	1992	51
Massive renal infarction due to mucormycosis in an AIDS patient J. Vesa, Óscar Bielsa, Octavio Arango, Infection Massive Renal InfarctionHivClinical Infectious Disease	1992	43
Identification of YAC clones for human chromosome 1p32 and physical mapping of the infantile neuronal ceroid lipofuscinosis (INCL) locus Elina Hellsten, J. Vesa, Mervi Heiskanen, Genomics Yac ClonesGenetic DisorderGeneticsHuman Chromosome 1P32Physical Mapping	1995	24
Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain Anna‐Liisa Fabritius, J. Vesa, Helena Minye, Experimental and Molecular Pathology Developmental BiologyMolecular NeuroscienceEpendymaNeuroanatomyDeveloping Mouse Brain	2014	20
The rearranged L-myc fusion gene (RLF) encodes a Zn-15 related zinc finger protein. Tomi P. Mäkelä, Elina Hellsten, J. Vesa, PubMed	1995	19
A Single PCR Marker in Strong Allelic Association with the Infantile Form of Neuronal Ceroid Lipofuscinosis Facilitates Reliable Prenatal Diagnostics and Disease Carrier Identification J. Vesa, Elina Hellsten, Tomi P. Mäkelä, European Journal of Human Genetics Disease Carrier IdentificationPathologyGynecologyInfantile FormSingle Pcr Marker	1993	19
DNA Diagnosis and Identification of Carriers of Infantile and Juvenile Neuronal Ceroid Lipofuscinoses Ann-Christine Syvänen, Irma Järvelä, T. Paunio, Neuropediatrics Early Prenatal DiagnosisGenetic TestingDna DiagnosisGenetic DisorderMedicine	1997	16

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