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Alexander Hoischen

Showing results (21-30 of 249) with videos related to

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European Journal of Human Genetics : EJHG|May 12, 2026
Transcription-based identification of uncharacterized genes in the human immune responseEmil E Vorsteveld, Simone Kersten, Charlotte Kaffa, et al.
Epilepsia|March 4, 2014
Exome sequencing identifies a de novo SCN2A mutation in a patient with intractable seizures, severe intellectual disability, optic atrophy, muscular hypotonia, and brain abnormalitiesAnna-Lena Baasch, Irina Hüning, Christian Gilissen, et al.
American Journal of Human Genetics|January 20, 2023
Comprehensive SMN1 and SMN2 profiling for spinal muscular atrophy analysis using long-read PacBio HiFi sequencingXiao Chen, John Harting, Emily Farrow, et al.
Nature Communications|May 6, 2017
Quantification of differential gene expression by multiplexed targeted resequencing of cDNAPeer Arts, Jori van der Raadt, Sebastianus H C van Gestel, et al.
European Journal of Neurology|January 6, 2025
Myotilin gene duplication causing late-onset myotilinopathyMarco Spinazzi, Marco Savarese, Franck Letournel, et al.
Molecular Therapy. Methods & Clinical Development|July 3, 2025
Repeat length as a key determinant for disease severity and antisense oligonucleotide activity in myotonic dystrophy type 1Najoua El Boujnouni, Lise Ripken, Marieke Willemse, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 8, 2010
Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridizationStefanie Weber, Christina Landwehr, Miriam Renkert, et al.
Scientific Reports|April 26, 2017
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentXiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2009
Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23Alexander Hoischen, Christina Landwehr, Sarah Kabisch, et al.
Geroscience|May 27, 2022
Circulating interleukin-37 declines with aging in healthy humans: relations to healthspan indicators and IL37 gene SNPsVienna E Brunt, Akpevweoghene P Ikoba, Brian P Ziemba, et al.
Pageof 25

Showing results (21-30 of 249) with videos related to

Sort By:
Pageof 25
European Journal of Human Genetics : EJHG|May 12, 2026
Transcription-based identification of uncharacterized genes in the human immune responseEmil E Vorsteveld, Simone Kersten, Charlotte Kaffa, et al.
Epilepsia|March 4, 2014
Exome sequencing identifies a de novo SCN2A mutation in a patient with intractable seizures, severe intellectual disability, optic atrophy, muscular hypotonia, and brain abnormalitiesAnna-Lena Baasch, Irina Hüning, Christian Gilissen, et al.
American Journal of Human Genetics|January 20, 2023
Comprehensive SMN1 and SMN2 profiling for spinal muscular atrophy analysis using long-read PacBio HiFi sequencingXiao Chen, John Harting, Emily Farrow, et al.
Nature Communications|May 6, 2017
Quantification of differential gene expression by multiplexed targeted resequencing of cDNAPeer Arts, Jori van der Raadt, Sebastianus H C van Gestel, et al.
European Journal of Neurology|January 6, 2025
Myotilin gene duplication causing late-onset myotilinopathyMarco Spinazzi, Marco Savarese, Franck Letournel, et al.
Molecular Therapy. Methods & Clinical Development|July 3, 2025
Repeat length as a key determinant for disease severity and antisense oligonucleotide activity in myotonic dystrophy type 1Najoua El Boujnouni, Lise Ripken, Marieke Willemse, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 8, 2010
Mapping candidate regions and genes for congenital anomalies of the kidneys and urinary tract (CAKUT) by array-based comparative genomic hybridizationStefanie Weber, Christina Landwehr, Miriam Renkert, et al.
Scientific Reports|April 26, 2017
Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairmentXiaowei Sylvia Chen, Rose H Reader, Alexander Hoischen, et al.
Pediatric Nephrology (Berlin, Germany)|May 16, 2009
Array-CGH in unclear syndromic nephropathies identifies a microdeletion in Xq22.3-q23Alexander Hoischen, Christina Landwehr, Sarah Kabisch, et al.
Geroscience|May 27, 2022
Circulating interleukin-37 declines with aging in healthy humans: relations to healthspan indicators and IL37 gene SNPsVienna E Brunt, Akpevweoghene P Ikoba, Brian P Ziemba, et al.
Pageof 25