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U Ludwig

Showing results (131-140 of 204) with videos related to

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Psychiatric Genetics|November 20, 2008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sampleKerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
NPJ Genomic Medicine|July 2, 2021
TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19Axel Schmidt, Sophia Peters, Alexej Knaus, et al.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Human Genetics|March 21, 2013
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio studyT H Beaty, M A Taub, A F Scott, et al.
Genomics Data|September 16, 2016
Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS dataEva Dunkhase, Kerstin U Ludwig, Michael Knapp, et al.
International Journal of Epidemiology|May 7, 2020
Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization studyChristina Dardani, Laurence J Howe, Nandita Mukhopadhyay, et al.
Plos Genetics|August 2, 2018
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphologyLaurence J Howe, Myoung Keun Lee, Gemma C Sharp, et al.
Translational Psychiatry|February 21, 2013
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adultsK U Ludwig, P Sämann, M Alexander, et al.
Pageof 21

Showing results (131-140 of 204) with videos related to

Sort By:
Pageof 21
Psychiatric Genetics|November 20, 2008
Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sampleKerstin U Ludwig, Johannes Schumacher, Gerd Schulte-Körne, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|April 8, 2014
Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin-1, a component of the bone morphogenetic protein 4 pathwayTaofik Al Chawa, Kerstin U Ludwig, Heide Fier, et al.
NPJ Genomic Medicine|July 2, 2021
TBK1 and TNFRSF13B mutations and an autoinflammatory disease in a child with lethal COVID-19Axel Schmidt, Sophia Peters, Alexej Knaus, et al.
International Journal of Pediatric Otorhinolaryngology|November 4, 2010
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patientsNilma Almeida de Assis, Stefanie Nowak, Kerstin U Ludwig, et al.
American Journal of Medical Genetics. Part A|February 28, 2012
A phenotype map for 14q32.3 terminal deletionsHartmut Engels, Herdit M Schüler, Alexander M Zink, et al.
Human Genetics|March 21, 2013
Confirming genes influencing risk to cleft lip with/without cleft palate in a case-parent trio studyT H Beaty, M A Taub, A F Scott, et al.
Genomics Data|September 16, 2016
Nonsyndromic cleft lip with or without cleft palate and cancer: Evaluation of a possible common genetic background through the analysis of GWAS dataEva Dunkhase, Kerstin U Ludwig, Michael Knapp, et al.
International Journal of Epidemiology|May 7, 2020
Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization studyChristina Dardani, Laurence J Howe, Nandita Mukhopadhyay, et al.
Plos Genetics|August 2, 2018
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphologyLaurence J Howe, Myoung Keun Lee, Gemma C Sharp, et al.
Translational Psychiatry|February 21, 2013
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adultsK U Ludwig, P Sämann, M Alexander, et al.
Pageof 21