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Michel Guipponi

Showing results (11-20 of 83) with videos related to

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Seizure|September 13, 2015
Familial epilepsy in Algeria: Clinical features and inheritance profilesAmina Chentouf, Aïcha Dahdouh, Michel Guipponi, et al.
Clinical Genetics|January 21, 2026
Biallelic MYH3 Variants Cause Distal Arthrogryposis in Compound Heterozygosity and a Subclinical Phenotype in Simple Heterozygosity. Codominance or Recessive Inheritance?Omar Zgheib, Thomas Rio-Frio, Michel Guipponi, et al.
Pediatric Diabetes|January 27, 2019
Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetesCaroline Stekelenburg, Karine Gerster, Jean-Louis Blouin, et al.
The American Journal of Psychiatry|August 19, 2009
Prevalence and heritability of compulsive hoarding: a twin studyAlessandra C Iervolino, Nader Perroud, Miguel Angel Fullana, et al.
ACG Case Reports Journal|August 14, 2023
Variable Intrafamilial Expression of ABCB4 DiseaseLucia Zampaglione, Anne-Laure Rougemont, Laura Rubbia-Brandt, et al.
Journal of Molecular Neuroscience : MN|December 3, 2009
SAGE analysis of genes differentially expressed in presymptomatic TgSOD1G93A transgenic mice identified cellular processes involved in early stage of ALS pathologyMichel Guipponi, Qiao-Xin Li, Lavinia Hyde, et al.
Gene|November 5, 2003
Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12Marc Friedli, Michel Guipponi, Sonia Bertrand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 7, 2010
Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victimsNader Perroud, Elizabeth Neidhart, Brice Petit, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
BMC Medical Genetics|May 20, 2020
LARS2-Perrault syndrome: a new case report and literature reviewMaria Teresa Carminho-Rodrigues, Phillipe Klee, Sacha Laurent, et al.
Pageof 9

Showing results (11-20 of 83) with videos related to

Sort By:
Pageof 9
Seizure|September 13, 2015
Familial epilepsy in Algeria: Clinical features and inheritance profilesAmina Chentouf, Aïcha Dahdouh, Michel Guipponi, et al.
Clinical Genetics|January 21, 2026
Biallelic MYH3 Variants Cause Distal Arthrogryposis in Compound Heterozygosity and a Subclinical Phenotype in Simple Heterozygosity. Codominance or Recessive Inheritance?Omar Zgheib, Thomas Rio-Frio, Michel Guipponi, et al.
Pediatric Diabetes|January 27, 2019
Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetesCaroline Stekelenburg, Karine Gerster, Jean-Louis Blouin, et al.
The American Journal of Psychiatry|August 19, 2009
Prevalence and heritability of compulsive hoarding: a twin studyAlessandra C Iervolino, Nader Perroud, Miguel Angel Fullana, et al.
ACG Case Reports Journal|August 14, 2023
Variable Intrafamilial Expression of ABCB4 DiseaseLucia Zampaglione, Anne-Laure Rougemont, Laura Rubbia-Brandt, et al.
Journal of Molecular Neuroscience : MN|December 3, 2009
SAGE analysis of genes differentially expressed in presymptomatic TgSOD1G93A transgenic mice identified cellular processes involved in early stage of ALS pathologyMichel Guipponi, Qiao-Xin Li, Lavinia Hyde, et al.
Gene|November 5, 2003
Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12Marc Friedli, Michel Guipponi, Sonia Bertrand, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 7, 2010
Simultaneous analysis of serotonin transporter, tryptophan hydroxylase 1 and 2 gene expression in the ventral prefrontal cortex of suicide victimsNader Perroud, Elizabeth Neidhart, Brice Petit, et al.
Human Genomics|July 17, 2016
Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreePeriklis Makrythanasis, Michel Guipponi, Federico A Santoni, et al.
BMC Medical Genetics|May 20, 2020
LARS2-Perrault syndrome: a new case report and literature reviewMaria Teresa Carminho-Rodrigues, Phillipe Klee, Sacha Laurent, et al.
Pageof 9