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U Ludwig

Showing results (111-120 of 204) with videos related to

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Molecular Psychiatry|July 24, 2009
Supporting evidence for LRRTM1 imprinting effects in schizophreniaK U Ludwig, M Mattheisen, T W Mühleisen, et al.
Genes|December 24, 2021
Iron Deficiency Caused by Intestinal Iron Loss-Novel Candidate Genes for Severe AnemiaCarolina Huettmann, Matthias Stelljes, Sugirthan Sivalingam, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothoraxSophia Schneider, Ricarda Köllges, Jil D Stegmann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2009
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexiaKerstin U Ludwig, Darina Roeske, Stefan Herms, et al.
Molecular Psychiatry|September 30, 2009
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic childrenD Roeske, K U Ludwig, N Neuhoff, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2014
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in YemenKhalid Ahmed Aldhorae, Anne C Böhmer, Kerstin U Ludwig, et al.
Translational Psychiatry|July 12, 2012
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spellingJ Becker, D Czamara, P Hoffmann, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patientsTiit Nikopensius, Laima Ambrozaityte, Kerstin U Ludwig, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patientsHartmut Engels, Eva Wohlleber, Alexander Zink, et al.
Psychiatric Genetics|March 9, 2017
Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxietyAndreas J Forstner, Stefanie Rambau, Nina Friedrich, et al.
Pageof 21

Showing results (111-120 of 204) with videos related to

Sort By:
Pageof 21
Molecular Psychiatry|July 24, 2009
Supporting evidence for LRRTM1 imprinting effects in schizophreniaK U Ludwig, M Mattheisen, T W Mühleisen, et al.
Genes|December 24, 2021
Iron Deficiency Caused by Intestinal Iron Loss-Novel Candidate Genes for Severe AnemiaCarolina Huettmann, Matthias Stelljes, Sugirthan Sivalingam, et al.
American Journal of Medical Genetics. Part A|January 7, 2022
Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothoraxSophia Schneider, Ricarda Köllges, Jil D Stegmann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2009
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexiaKerstin U Ludwig, Darina Roeske, Stefan Herms, et al.
Molecular Psychiatry|September 30, 2009
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic childrenD Roeske, K U Ludwig, N Neuhoff, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2014
Nonsyndromic cleft lip with or without cleft palate in arab populations: genetic analysis of 15 risk loci in a novel case-control sample recruited in YemenKhalid Ahmed Aldhorae, Anne C Böhmer, Kerstin U Ludwig, et al.
Translational Psychiatry|July 12, 2012
Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spellingJ Becker, D Czamara, P Hoffmann, et al.
American Journal of Medical Genetics. Part A|October 20, 2009
Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patientsTiit Nikopensius, Laima Ambrozaityte, Kerstin U Ludwig, et al.
European Journal of Human Genetics : EJHG|May 28, 2009
A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patientsHartmut Engels, Eva Wohlleber, Alexander Zink, et al.
Psychiatric Genetics|March 9, 2017
Further evidence for genetic variation at the serotonin transporter gene SLC6A4 contributing toward anxietyAndreas J Forstner, Stefanie Rambau, Nina Friedrich, et al.
Pageof 21