Published in BMJ on December 14, 2012
Reconstructing the life of an unknown (ca. 500 years-old South American Inca) mummy--multidisciplinary study of a Peruvian Inca mummy suggests severe Chagas disease and ritual homicide. PLoS One (2014) 0.91
Checklist and Scoring System for the Assessment of Soft Tissue Preservation in CT Examinations of Human Mummies. PLoS One (2015) 0.87
The complete mitogenome of a 500-year-old Inca child mummy. Sci Rep (2015) 0.76
Identification of proteins from 4200-year-old skin and muscle tissue biopsies from ancient Egyptian mummies of the first intermediate period shows evidence of acute inflammation and severe immune response. Philos Trans A Math Phys Eng Sci (2016) 0.75
Evidence of neurofibromatosis type 1 in a multi-morbid Inca child mummy: A paleoradiological investigation using computed tomography. PLoS One (2017) 0.75
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
Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome. Nat Med (2011) 1.84
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
Microcephaly, malformation of brain development and intracranial calcification in sibs: pseudo-TORCH or a new syndrome. Am J Med Genet A (2008) 1.65
Tuberculosis: from prehistory to Robert Koch, as revealed by ancient DNA. Lancet Infect Dis (2004) 1.43
Mummified daughters of King Tutankhamun: archeologic and CT studies. AJR Am J Roentgenol (2011) 1.42
Leishmaniasis in ancient Egypt and Upper nubia. Emerg Infect Dis (2006) 1.27
Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. Hum Mol Genet (2009) 1.21
The iceman: discovery and imaging. Radiology (2003) 1.06
Genetic heterogeneity of deafness phenotypes linked to DFNA4. Am J Med Genet A (2005) 1.05
Evidence for a 7000-year-old case of primary hyperparathyroidism. JAMA (2005) 1.03
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
Comment on "The brain of LB1, Homo floresiensis". Science (2005) 1.00
Interleukin-18 expression and the response to treatment in patients with psoriasis. Arch Med Sci (2011) 0.99
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
Gastric adenocarcinoma has a unique microRNA signature not present in esophageal adenocarcinoma. Cancer (2013) 0.95
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
Isolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina. Invest Ophthalmol Vis Sci (2003) 0.93
Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genet Cytogenet (2004) 0.92
Magnetic resonance imaging in fetal anomalies: What does it add to 3D and 4D US? Eur J Radiol (2009) 0.91
Cytokine regulation of the trefoil factor family binding protein GKN2 (GDDR/TFIZ1/blottin) in human gastrointestinal epithelial cells. Cell Physiol Biochem (2007) 0.91
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
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
Epigenetic alterations by methylation of RASSF1A and DAPK1 promoter sequences in mammary carcinoma detected in extracellular tumor DNA. Cancer Genet Cytogenet (2010) 0.85
Plasmodium falciparum in ancient Egypt. Emerg Infect Dis (2008) 0.84
Multidetector CT investigation of the mummy of Rosalia Lombardo (1918-1920). Ann Anat (2013) 0.84
Autoimmune retinopathy with RPE hypersensitivity and 'negative ERG' in X-linked hyper-IgM syndrome. Ocul Immunol Inflamm (2005) 0.83
Scenes from the past: radiologic evidence of anthropogenic mummification in the Capuchin Catacombs of Palermo, Sicily. Radiographics (2010) 0.82
Herniation pits in human mummies: a CT investigation in the Capuchin Catacombs of Palermo, Sicily. PLoS One (2012) 0.82
A decade in search of myopia genes. Front Biosci (Landmark Ed) (2010) 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
Liposomes as an ocular delivery system of fluconazole: in-vitro studies. Acta Ophthalmol (2010) 0.79
Liposomal gels for site-specific, sustained delivery of celecoxib: in vitro and in vivo evaluation. Drug Dev Res (2014) 0.79
Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness. Int J Mol Med (2005) 0.79
Molecular identification of falciparum malaria and human tuberculosis co-infections in mummies from the Fayum depression (Lower Egypt). PLoS One (2013) 0.78
Molecular analysis of 5alpha-reductase type 2 gene in eight unrelated egyptian children with suspected 5alpha-reductase deficiency: prevalence of the G34R mutation. Clin Endocrinol (Oxf) (2003) 0.78
Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis. Cell Physiol Biochem (2008) 0.78
Fossil record of meningioma. Lancet (2003) 0.78
Diencephalic-mesencephalic junction dysplasia: a novel recessive brain malformation. Brain (2012) 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
Paleopathological examination of medieval spines with exceptional thoracic kyphosis most likely secondary to spinal tuberculosis. Historical vignette. J Neurosurg Spine (2004) 0.78
Transdermal delivery of meloxicam using niosomal hydrogels: in vitro and pharmacodynamic evaluation. Pharm Dev Technol (2014) 0.77
New recessive syndrome of microcephaly, cerebellar hypoplasia, and congenital heart conduction defect. Am J Med Genet A (2011) 0.77
The Salafia method rediscovered. Virchows Arch (2009) 0.76
Fetal brain disruption sequence versus fetal brain arrest: A distinct autosomal recessive developmental brain malformation phenotype. Am J Med Genet A (2015) 0.75
Interleukin-18 expression and the response to treatment in patients with psoriasis. Arch Med Sci (2010) 0.75
Archaeology and prevalence of Paget's disease. J Bone Miner Res (2005) 0.75
Detection of bone glue treatment as a major source of contamination in ancient DNA analyses. Am J Phys Anthropol (2002) 0.75
Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin gene. Int J Mol Med (2003) 0.75
A novel double mutation in the luteinizing hormone receptor in a kindred with familial Leydig cell hypoplasia and male pseudohermaphroditism. Endocr Res (2005) 0.75
Reduced expression of connexin 31.1 in larynx cancer is not caused by GJB5 mutations. Cancer Lett (2004) 0.75
Enlightening the past: analytical proof for the use of Pistacia exudates in ancient Egyptian embalming resins. J Sep Sci (2011) 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
A new long-acting liposomal topical antifungal formula: human clinical study. Cornea (2012) 0.75
Profound microcephaly, primordial dwarfism with developmental brain malformations: a new syndrome. Am J Med Genet A (2012) 0.75