Published in Am J Phys Anthropol on June 01, 2002
Ancestry and pathology in King Tutankhamun's family. JAMA (2010) 6.31
New insights into the Tyrolean Iceman's origin and phenotype as inferred by whole-genome sequencing. Nat Commun (2012) 3.18
Complete mitochondrial genome of a Pleistocene jawbone unveils the origin of polar bear. Proc Natl Acad Sci U S A (2010) 2.57
Reconstructing mitochondrial genomes directly from genomic next-generation sequencing reads--a baiting and iterative mapping approach. Nucleic Acids Res (2013) 2.08
Polar and brown bear genomes reveal ancient admixture and demographic footprints of past climate change. Proc Natl Acad Sci U S A (2012) 1.98
Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). Am J Hum Genet (2004) 1.67
Molecular phylogeny of the Athetini-Lomechusini-Ecitocharini clade of aleocharine rove beetles (Insecta). Zool Scr (2012) 1.31
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. Hum Mol Genet (2009) 1.21
Spiking of contemporary human template DNA with ancient DNA extracts induces mutations under PCR and generates nonauthentic mitochondrial sequences. Mol Biol Evol (2004) 1.11
Genetic heterogeneity of deafness phenotypes linked to DFNA4. Am J Med Genet A (2005) 1.05
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina. Eur J Hum Genet (2002) 1.03
Phylogeny of the tribe Athetini (Coleoptera: Staphylinidae) inferred from mitochondrial and nuclear sequence data. Mol Phylogenet Evol (2010) 1.01
Mitochondrial DNA variation of Gyrodactylus spp (Monogenea, Gyrodactylidae) populations infecting Atlantic salmon, grayling, and rainbow trout in Norway and Sweden. Int J Parasitol (2003) 1.01
Functional relevance of ceruloplasmin mutations in Parkinson's disease. FASEB J (2005) 1.00
Comment on "The brain of LB1, Homo floresiensis". Science (2005) 1.00
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease. Hum Genet (2006) 1.00
Yersinial F1 antigen and the cause of Black Death. Lancet Infect Dis (2004) 0.99
Temporal and spatial analyses disclose consequences of habitat fragmentation on the genetic diversity in capercaillie (Tetrao urogallus). Mol Ecol (2008) 0.99
Cardiomyopathy in Friedreich's ataxia-assessment by cardiac MRI. Mov Disord (2007) 0.99
The use of morphometric characters to discriminate specimens of laboratory-reared and wild populations of Gyrodactylus salaris and G. thymalli (Monogenea). Folia Parasitol (Praha) (2004) 0.98
Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping. Int J Mol Med (2008) 0.98
DNA phasing by TA dinucleotide microsatellite length determines in vitro and in vivo expression of the gp91phox subunit of NADPH oxidase and mediates protection against severe malaria. J Infect Dis (2004) 0.97
Substantial loss of conserved and gain of novel MicroRNA families in flatworms. Mol Biol Evol (2013) 0.96
First insights into the metagenome of Egyptian mummies using next-generation sequencing. J Appl Genet (2013) 0.95
Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene. Graefes Arch Clin Exp Ophthalmol (2002) 0.94
A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness. Am J Ophthalmol (2003) 0.93
Aberrant expression of the homeobox gene CDX2 in pediatric acute lymphoblastic leukemia. Blood (2009) 0.93
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina. Invest Ophthalmol Vis Sci (2003) 0.93
Microsatellite evolution: Mutations, sequence variation, and homoplasy in the hypervariable avian microsatellite locus HrU10. BMC Evol Biol (2008) 0.93
Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients. Mol Genet Metab (2004) 0.92
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genet Cytogenet (2004) 0.92
Cytokine regulation of the trefoil factor family binding protein GKN2 (GDDR/TFIZ1/blottin) in human gastrointestinal epithelial cells. Cell Physiol Biochem (2007) 0.91
The complete mitochondrial DNA sequence of the monogenean Gyrodactylus thymalli (Platyhelminthes: Monogenea), a parasite of grayling (Thymallus thymallus). Mol Biochem Parasitol (2007) 0.90
Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form. Hum Mol Genet (2008) 0.90
Analysis of molecular data of Arabidopsis thaliana (L.) Heynh. (Brassicaceae) with Geographical Information Systems (GIS). Mol Ecol (2003) 0.89
Mitochondrial haplotype diversity of Gyrodactylus thymalli (Platyhelminthes; Monogenea): extended geographic sampling in United Kingdom, Poland, and Norway reveals further lineages. Parasitol Res (2007) 0.88
Cytotoxic activity of natural killer cells lacking killer-inhibitory receptors for self-HLA class I molecules against autologous hematopoietic stem cells in healthy individuals. Exp Mol Pathol (2004) 0.88
Comparative genomics of flatworms (platyhelminthes) reveals shared genomic features of ecto- and endoparastic neodermata. Genome Biol Evol (2014) 0.88
MicroRNA preparations from individual monogenean Gyrodactylus salaris-a comparison of six commercially available totalRNA extraction kits. BMC Res Notes (2011) 0.87
Molecular phylogeny and taxonomic revision of the sportive lemurs (Lepilemur, Primates). BMC Evol Biol (2006) 0.87
Phylogeography and mitochondrial DNA divergence in Dolichopoda cave crickets (Orthoptera, Rhahidophoridae). Hereditas (2009) 0.86
Revisiting the harem conspiracy and death of Ramesses III: anthropological, forensic, radiological, and genetic study. BMJ (2012) 0.86
Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA. Cancer Genet Cytogenet (2010) 0.85
Transgenic overexpression of the alpha-synuclein interacting protein synphilin-1 leads to behavioral and neuropathological alterations in mice. Neurogenetics (2010) 0.85
DNA taxonomy and barcoding of monogenean parasites: lessons from Gyrodactylus. Trends Parasitol (2007) 0.85
Basics in paleodemography: a comparison of age indicators applied to the early medieval skeletal sample of Lauchheim. Am J Phys Anthropol (2008) 0.83
Transcranial ultrasound in different monogenetic subtypes of Parkinson's disease. J Neurol (2007) 0.83
Phylogenetic footprinting of non-coding RNA: hammerhead ribozyme sequences in a satellite DNA family of Dolichopoda cave crickets (Orthoptera, Rhaphidophoridae). BMC Evol Biol (2010) 0.83
Paleopathological features of the cervical spine in the early middle ages: natural history of degenerative diseases. Neurosurgery (2003) 0.83
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndrome. Ocul Immunol Inflamm (2005) 0.83
Lateral angle: a method for sexing using the petrous bone. Am J Phys Anthropol (2005) 0.82
Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigra. Neurosci Lett (2006) 0.82
Sex-specific recombination rates in Parus major and P. caeruleus, an exception to Huxley's rule. Hereditas (2003) 0.81
A decade in search of myopia genes. Front Biosci (Landmark Ed) (2010) 0.81
Molecular evolution of the pDo500 satellite DNA family in Dolichopoda cave crickets (Rhaphidophoridae). BMC Evol Biol (2009) 0.81
Visceral Leishmaniasis during Italian Renaissance, 1522-1562. Emerg Infect Dis (2012) 0.80
Population haplotypes of exon ORF15 of the retinitis pigmentosa GTPase regulator gene in Germany : implications for screening for inherited retinal disorders. Mol Diagn Ther (2006) 0.80
A globally occurring indel polymorphism in the promoter of the IFNA2 gene is not associated with severity of malaria but with the positivity rate of HCV. BMC Genet (2008) 0.80
Variant alleles of the mannose binding lectin 2 gene (MBL2) confer heterozygote advantage within Crohn's families. Scand J Gastroenterol (2010) 0.80
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach. Eur J Hum Genet (2006) 0.79
Molecular characterization of regulatory polymorphisms in the promoter region of the STAT6 gene in a Gabonese population. Mem Inst Oswaldo Cruz (2011) 0.79
Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness. Int J Mol Med (2005) 0.79
Correction: Implications of the circumpolar genetic structure of polar bears for their conservation in a rapidly warming Arctic. PLoS One (2015) 0.78
Molecular identification of falciparum malaria and human tuberculosis co-infections in mummies from the Fayum depression (Lower Egypt). PLoS One (2013) 0.78
Mutational risk in highly repetitive exon ORF15 of the RPGR multidisease gene is not associated with haplotype background. Int J Mol Med (2005) 0.78
Fossil record of meningioma. Lancet (2003) 0.78
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis. Cell Physiol Biochem (2008) 0.78
Paleopathological examination of medieval spines with exceptional thoracic kyphosis most likely secondary to spinal tuberculosis. Historical vignette. J Neurosurg Spine (2004) 0.78
Morphometric and molecular characterization of Gyrodactylus teuchis Lautraite, Blanc, Thiery, Daniel & Vigneulle, 1999 (Monogenea: Gyrodactylidae) from an Austrian brown trout population. Parasitol Int (2011) 0.77
Unexpected early extinction of the European pond turtle (Emys orbicularis) in Sweden and climatic impact on its Holocene range. Mol Ecol (2009) 0.76
Seasonal prevalence of Lyme disease spirochetes in a heterothermic mammal, the edible dormouse (Glis glis). Appl Environ Microbiol (2014) 0.76
CAG repeats in Restless Legs syndrome. Am J Med Genet B Neuropsychiatr Genet (2006) 0.75
Archaeology and prevalence of Paget's disease. J Bone Miner Res (2005) 0.75
Comments on: evolutionary and statistical properties of three genetic distances (Kalinowski, 2002). Mol Ecol (2003) 0.75
An intron-containing, heat-inducible stress-70 gene in the millipede Tachypodoiulus niger (Julidae, Diplopoda). Cell Stress Chaperones (2014) 0.75
Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations. Cancer Lett (2004) 0.75
Fronto-ethmoidal encephalocele in a historical skull with artificial deformation and no signs of chronic elevated intracranial pressure. Acta Neurochir (Wien) (2008) 0.75
Enlightening the past: analytical proof for the use of Pistacia exudates in ancient Egyptian embalming resins. J Sep Sci (2011) 0.75
Mitochondrial DNA variation of a natural population of Gyrodactylus thymalli (Monogenea) from the type locality River Hnilec, Slovakia. Parasitol Res (2007) 0.75
High genetic variability of esterase loci in natural populations of Parus major, P. caeruleus, and P. ater. Biochem Genet (2004) 0.75
Studies of S-adenosylhomocysteine-hydrolase polymorphism in a Croatian population. J Hum Genet (2005) 0.75
Documenting ancient DNA quality via alpha satellite amplification and assessment of clone sequence diversity. J Appl Genet (2002) 0.75
Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin gene. Int J Mol Med (2003) 0.75
Lumbar spine fracture in a 34,100-year-old skeleton: the oldest known prehistoric spine fracture. Neurosurgery (2004) 0.75