PubRank

Ingo Kennerknecht

Author PubWeight™ 14.73‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21. Eur J Hum Genet 2008 1.90
2 A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy. Mol Vis 2006 1.20
3 Hereditary prosopagnosia: the first case series. Cortex 2007 1.10
4 Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies. Am J Med Genet A 2004 1.01
5 Unexpected island effects at an extreme: reduced Y chromosome and mitochondrial DNA diversity in Nias. Mol Biol Evol 2010 0.91
6 Deficits in long-term recognition memory reveal dissociated subtypes in congenital prosopagnosia. PLoS One 2011 0.89
7 Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII and variants - update 2012. Eur J Hum Genet 2012 0.88
8 Gaze behaviour in hereditary prosopagnosia. Psychol Res 2006 0.83
9 The early time course of compensatory face processing in congenital prosopagnosia. PLoS One 2010 0.81
10 Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3. Hum Genet 2015 0.79
11 Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene? Eur J Hum Genet 2005 0.79
12 Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome). Acta Paediatr 2011 0.78
13 Sorting chromosomes as a software-based exercise. Med Educ 2010 0.76
14 Multicolor karyotyping in acute myeloid leukemia. Leuk Lymphoma 2003 0.76
15 Galactose uncovers face recognition and mental images in congenital prosopagnosia: the first case report. Nutr Neurosci 2013 0.75
16 Clinical utility gene card for: Ehlers-Danlos syndrome types I-VII. Eur J Hum Genet 2010 0.75
17 Novel der(1)t(1;19) in two patients with myeloid neoplasias. Cancer Genet Cytogenet 2002 0.75
18 A computational model of dysfunctional facial encoding in congenital prosopagnosia. Neural Netw 2011 0.75