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Thomas Josse

Showing results (11-20 of 25) with videos related to

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Biomedicines|September 23, 2022
SARS-CoV-2 Variability in Patients and Wastewaters-Potential Immuno-Modulation during the Shift from Delta to OmicronAhlam Chaqroun, Cédric Hartard, Thomas Josse, et al.
Macromolecular Rapid Communications|August 30, 2016
Synthesis and Characterization of Double Crystalline Cyclic Diblock Copolymers of Poly(ε-caprolactone) and Poly(l(d)-lactide) (c(PCL-b- PL(D)LA))Romain Liénard, Nerea Zaldua, Thomas Josse, et al.
Human Genomics|February 5, 2023
Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive casesTom Alix, Céline Chéry, Thomas Josse, et al.
The American Journal of Clinical Nutrition|March 9, 2019
Vitamin B-12 and liver activity and expression of methionine synthase are decreased in fetuses with neural tube defectsMa'atem B Fofou-Caillierez, Rosa-Maria Guéant-Rodriguez, Jean-Marc Alberto, et al.
Human Genetics|May 30, 2019
Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathwayEmeline Renard, Céline Chéry, Abderrahim Oussalah, et al.
Medicine|June 4, 2015
Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant ArticleAbderrahim Oussalah, Paolo Bosco, Guido Anello, et al.
Allergy|October 23, 2021
Next-generation sequencing and genotype association studies reveal the association of HLA-DRB3*02:02 with delayed hypersensitivity to penicillinsAntonino Romano, Abderrahim Oussalah, Celine Chery, et al.
Biochimie|February 14, 2013
Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variantCeline Chery, Alain Hehn, Nadir Mrabet, et al.
Journal of Medical Genetics|August 19, 2016
Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populationsLaetitia Goffinet, Abderrahim Oussalah, Rosa-Maria Guéant-Rodriguez, et al.
Ebiomedicine|April 9, 2018
Plasma mSEPT9: A Novel Circulating Cell-free DNA-Based Epigenetic Biomarker to Diagnose Hepatocellular CarcinomaAbderrahim Oussalah, Susann Rischer, Mouni Bensenane, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Biomedicines|September 23, 2022
SARS-CoV-2 Variability in Patients and Wastewaters-Potential Immuno-Modulation during the Shift from Delta to OmicronAhlam Chaqroun, Cédric Hartard, Thomas Josse, et al.
Macromolecular Rapid Communications|August 30, 2016
Synthesis and Characterization of Double Crystalline Cyclic Diblock Copolymers of Poly(ε-caprolactone) and Poly(l(d)-lactide) (c(PCL-b- PL(D)LA))Romain Liénard, Nerea Zaldua, Thomas Josse, et al.
Human Genomics|February 5, 2023
Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive casesTom Alix, Céline Chéry, Thomas Josse, et al.
The American Journal of Clinical Nutrition|March 9, 2019
Vitamin B-12 and liver activity and expression of methionine synthase are decreased in fetuses with neural tube defectsMa'atem B Fofou-Caillierez, Rosa-Maria Guéant-Rodriguez, Jean-Marc Alberto, et al.
Human Genetics|May 30, 2019
Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathwayEmeline Renard, Céline Chéry, Abderrahim Oussalah, et al.
Medicine|June 4, 2015
Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant ArticleAbderrahim Oussalah, Paolo Bosco, Guido Anello, et al.
Allergy|October 23, 2021
Next-generation sequencing and genotype association studies reveal the association of HLA-DRB3*02:02 with delayed hypersensitivity to penicillinsAntonino Romano, Abderrahim Oussalah, Celine Chery, et al.
Biochimie|February 14, 2013
Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variantCeline Chery, Alain Hehn, Nadir Mrabet, et al.
Journal of Medical Genetics|August 19, 2016
Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populationsLaetitia Goffinet, Abderrahim Oussalah, Rosa-Maria Guéant-Rodriguez, et al.
Ebiomedicine|April 9, 2018
Plasma mSEPT9: A Novel Circulating Cell-free DNA-Based Epigenetic Biomarker to Diagnose Hepatocellular CarcinomaAbderrahim Oussalah, Susann Rischer, Mouni Bensenane, et al.
Pageof 3