Albert de la Chapelle

Author

University of Helsinki

Also Known As

A de la Chapelle, Albert de la Chapelle

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki Folkhälsans Forskningscentrum Helsinki Children's Hospital Helsinki University Hospital Väestöliitto

About

Albert de la Chapelle is an author at University of Helsinki specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	1.2K
2	Natural Sciences	2	2	596
3	Biology	2	2	596
4	Health Sciences	1	1	11
5	Public Health	1	1	12

Albert de la Chapelle

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland Johanna Hästbacka, Albert de la Chapelle, Ilkka Kaitila, Nature Genetics BiologyLinkage DisequilibriumDiastrophic DysplasiaLinkage Disequilibrium MappingMolecular Ecology	1992	565
Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia Maaret Ridanpää, Hans van Eenennaam, Katarina Pelin, Cell Cartilage-hair HypoplasiaGeneticsRna BiologyPathologyRnase Mrp Cause	2001	509
The Use and Misuse of Sex Chromatin Screening for `Gender Identification' of Female Athletes Albert de la Chapelle JAMA	1986	67
Cystic fibrosis in a low-incidence population: two major mutations in Finland Juha Kere, Xavier Estivill, Miguel Chillón, Human Genetics FibrosisMendelian DisorderLow-incidence PopulationMedicinePathology	1994	51
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. Kimmo Virtaneva, Jinmin Miao, A L Träskelin, PubMed	1996	37
Linkage relationships and gene order around the locus for X-linked retinoschisis. Tiina Alitalo, H Forsius, Jussi Kärnä, PubMed	1988	34
In situ localization and characterization of different classes of chromosomal DNA: acridine orange and quinacrine mustard fluorescence Albert de la Chapelle, Jim Schröder, Ritva-Kajsa Selander Chromosoma BiologyChromatinDna SequencingDnaCytogenetics	1973	31
Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq. Petri Saviranta, Mikael Lindlöf, A E Lehesjoki, PubMed	1988	18
Cystic fibrosis mutation ΔF508 in Finland: other mutations predominate Juha Kere, Erkki Savilahti, Reijo Norio, Human Genetics Molecular Diagnostic TechniquesMendelian DisorderGenetic DisorderMedicineGenetics	1990	12
Chromosome 12 in human testicular cancer: Dosage changes and their parental origin Païvi Peltomäki, Ragnhild A. Lothe, Anne‐Lise Børresen, Cancer Genetics and Cytogenetics Human Testicular CancerCytogeneticsMedicinePathologyChromosome Biology	1992	11

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