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American Journal of Human Genetics|February 11, 1999
Comparison of the power and accuracy of biallelic and microsatellite markers in population-based gene-mapping methodsM Xiong, L JinAmerican Journal of Human Genetics|July 1, 1991
Estimation of morbid risk and age at onset with missing informationL A Cupples, N Risch, L A Farrer, et al.American Journal of Human Genetics|December 1, 1991
A new glucocerebrosidase-gene missense mutation responsible for neuronopathic Gaucher disease in Japanese patientsH Kawame, Y EtoAmerican Journal of Human Genetics|March 6, 2008
A critical appraisal of the scientific basis of commercial genomic profiles used to assess health risks and personalize health interventionsA Cecile J W Janssens, Marta Gwinn, Linda A Bradley, et al.American Journal of Human Genetics|March 6, 2008
Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individualsCornelis A Albers, Jim Stankovich, Russell Thomson, et al.American Journal of Human Genetics|March 6, 2008
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiencyClotilde Lagier-Tourenne, Meriem Tazir, Luis Carlos López, et al.American Journal of Human Genetics|March 6, 2008
Estimating ethnic admixture from pedigree dataJanet S Sinsheimer, Christopher L Plaisier, Adriana Huertas-Vazquez, et al.American Journal of Human Genetics|January 9, 2008
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk cultureNabil Sabri Enattah, Tine G K Jensen, Mette Nielsen, et al.American Journal of Human Genetics|January 9, 2008
Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosisKen Arita, Andrew P South, Günter Hans-Filho, et al.American Journal of Human Genetics|January 9, 2008
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35Rob W J Collin, Ersan Kalay, Muhammad Tariq, et al.Pageof 979