| PCSK6 VNTR Polymorphism Is Associated with Degree of Handedness but Not Direction of Handedness L Arning, S Ocklenburg, S Schulz, V Ness, WM Gerding, JG Hengstler, ... PLoS One 8 (6), e67251, 2013 | 99 | 2013 |
| Handedness and the X chromosome: the role of androgen receptor CAG-repeat length L Arning, S Ocklenburg, S Schulz, V Ness, WM Gerding, JG Hengstler, ... Scientific Reports 5 (1), 8325, 2015 | 68 | 2015 |
| Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization S Ocklenburg, L Arning, C Hahn, WM Gerding, JT Epplen, O Güntürkün, ... Behavioural brain research 225 (1), 284-289, 2011 | 61 | 2011 |
| FOXP2 variation modulates functional hemispheric asymmetries for speech perception S Ocklenburg, L Arning, WM Gerding, JT Epplen, O Güntürkün, C Beste Brain and language 126 (3), 279-284, 2013 | 59 | 2013 |
| Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene G Dekomien, C Vollrath, E Petrasch-Parwez, MH Boevé, DA Akkad, ... Neurogenetics 11, 163-174, 2010 | 59 | 2010 |
| Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization S Ocklenburg, L Arning, WM Gerding, JT Epplen, O Güntürkün, C Beste PLoS One 8 (1), e53643, 2013 | 44 | 2013 |
| Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF WM Gerding, J Koetting, JT Epplen, C Neusch Neuromuscular Disorders 19 (10), 701-703, 2009 | 43 | 2009 |
| Ccdc66 null mutation causes retinal degeneration and dysfunction WM Gerding, S Schreiber, T Schulte-Middelmann, A de Castro Marques, ... Human molecular genetics 20 (18), 3620-3631, 2011 | 42 | 2011 |
| Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patients WM Gerding, M Tembrink, V Nilius‐Eliliwi, T Mika, F Dimopoulos, ... International Journal of Cancer 150 (12), 1998-2011, 2022 | 41 | 2022 |
| Exome sequencing reveals AGBL5 as novel candidate gene and additional variants for retinitis pigmentosa in five Turkish families S Kastner, IJ Thiemann, G Dekomien, E Petrasch-Parwez, S Schreiber, ... Investigative ophthalmology & visual science 56 (13), 8045-8053, 2015 | 37 | 2015 |
| Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene R Kropatsch, E Petrasch-Parwez, D Seelow, A Schlichting, WM Gerding, ... Molecular and cellular probes 24 (6), 357-363, 2010 | 31 | 2010 |
| Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes G Aydin, G Dekomien, S Hoffjan, WM Gerding, JT Epplen, L Arning BMC neurology 18, 1-8, 2018 | 28 | 2018 |
| Left-Right Axis Differentiation and Functional Lateralization: a Haplotype in the Methyltransferase Encoding Gene SETDB2 Might Mediate Handedness in Healthy … S Ocklenburg, L Arning, WM Gerding, JG Hengstler, JT Epplen, ... Molecular neurobiology 53, 6355-6361, 2016 | 26 | 2016 |
| SOX9 Duplication Linked to Intersex in Deer R Kropatsch, G Dekomien, DA Akkad, WM Gerding, E Petrasch-Parwez, ... PloS one 8 (9), e73734, 2013 | 23 | 2013 |
| Myelin Water Fraction Imaging Reveals Hemispheric Asymmetries in Human White Matter That Are Associated with Genetic Variation in PLP1 S Ocklenburg, C Anderson, WM Gerding, C Fraenz, C Schlüter, ... Molecular neurobiology 56, 3999-4012, 2019 | 21 | 2019 |
| Optical genome mapping for cytogenetic diagnostics in AML V Nilius-Eliliwi, WM Gerding, R Schroers, HP Nguyen, DB Vangala Cancers 15 (6), 1684, 2023 | 20* | 2023 |
| Unusual Charcot–Marie–Tooth phenotype due to a mutation within the intracellular domain of myelin protein zero C Schneider‐Gold, J Kötting, JT Epplen, R Gold, WM Gerding Muscle & Nerve: Official Journal of the American Association of …, 2010 | 20 | 2010 |
| Late onset Alexander’s disease presenting as cerebellar ataxia associated with a novel mutation in the GFAP gene S Schmidt, MP Wattjes, WM Gerding, M van der Knaap Journal of neurology 258, 938-940, 2011 | 19 | 2011 |
| Homozygosity mapping and sequencing identify two genes that might contribute to pointing behavior in hunting dogs DA Akkad, WM Gerding, RB Gasser, JT Epplen Canine Genetics and Epidemiology 2, 1-13, 2015 | 16 | 2015 |
| Cognitive Control Processes and Functional Cerebral Asymmetries: Association with Variation in the Handedness-Associated Gene LRRTM1 C Beste, L Arning, WM Gerding, JT Epplen, A Mertins, MC Röder, JJ Bless, ... Molecular Neurobiology 55, 2268-2274, 2018 | 13 | 2018 |
