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List of works by Christian Andres

1H-13C NMR-based urine metabolic profiling in autism spectrum disorders.

scientific article published on 9 April 2013

1H-NMR-based metabolomic profiling of CSF in early amyotrophic lateral sclerosis

scientific article

A case of severe toxicity during coadministration of vincristine and piperacillin: are drug transporters involved in vincristine hypersensitivity and drug-drug interactions?

scientific article published on 01 November 2012

A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population

scientific article published on 17 June 2015

A decrease in blood cholesterol after gastrostomy could impact survival in ALS.

scientific article published on 19 April 2017

A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma.

scientific article

A novel mutation in the cleavage site N291 of TDP-43 protein in a familial case of amyotrophic lateral sclerosis

scientific article published on 17 April 2020

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS.

scientific article published on 5 January 2017

A prospective study of estimated glomerular filtration rate and outcomes in patients with atrial fibrillation: the Loire Valley Atrial Fibrillation Project.

scientific article published in June 2014

A rare motor neuron deleterious missense mutation in the DPYSL3 (CRMP4) gene is associated with ALS.

scientific article published on 28 May 2013

A unique hydrophobic domain of rat brain globular acetylcholinesterase for binding to cell membranes

scientific article published on December 1, 1992

ABCB4 gene mutations and single-nucleotide polymorphisms in women with intrahepatic cholestasis of pregnancy.

scientific article published on 6 July 2009

ANNALS EXPRESS: Post-hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability

scientific article published in January 2018

APOE ε4 allele is associated with an increased risk of bulbar-onset amyotrophic lateral sclerosis in men

scientific article published on 20 January 2011

Absence of the OPTN mutation in a patient with ALS and familial primary open angle glaucoma

scientific article published on 17 August 2011

Acetylcholinesterase-transgenic mice display embryonic modulations in spinal cord choline acetyltransferase and neurexin Iβ gene expression followed by late-onset neuromotor deterioration ⬇️

scientific article published on July 22, 1997

Advances in cellular models to explore the pathophysiology of amyotrophic lateral sclerosis.

scientific article

Amyotrophic Lateral Sclerosis, 2016: existing therapies and the ongoing search for neuroprotection.

scientific article published on 29 June 2016

An UPLC-MSMS method to measure plasma homocysteine concentration.

scientific article published in June 2017

Analytical methodology for metabolomics study of adherent mammalian cells using NMR, GC-MS and LC-HRMS.

scientific article published on 7 October 2015

Association between divalent metal transport 1 encoding gene (SLC11A2) and disease duration in amyotrophic lateral sclerosis

scientific article

Association of a functional deficit of the BKCa channel, a synaptic regulator of neuronal excitability, with autism and mental retardation

scientific article

Association of a paraneoplastic motor neuron disease with anti-Ri antibodies and a novel SOD1 I18del mutation.

scientific article

Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level

scientific article published on 9 July 2009

Behavior and serotonergic disorders in rats exposed prenatally to valproate: a model for autism

scientific article published on 28 December 2009

Benign lower limb amyotrophy due to TARDBP mutation or post-polio syndrome?

scientific article

Biological follow-up in amyotrophic lateral sclerosis: decrease in creatinine levels and increase in ferritin levels predict poor prognosis.

scientific article published on 22 June 2015

Biomarkers in amyotrophic lateral sclerosis: combining metabolomic and clinical parameters to define disease progression.

scientific article published on 28 October 2015

Blood Cell Palmitoleate-Palmitate Ratio Is an Independent Prognostic Factor for Amyotrophic Lateral Sclerosis

scientific article

C-reactive protein: A promising biomarker in ALS?

scientific article published on 7 August 2017

Causative Genes in Amyotrophic Lateral Sclerosis and Protein Degradation Pathways: a Link to Neurodegeneration.

scientific article published on 10 January 2018

Chronic demyelinating polyneuropathy and B6 hypervitaminosis

scientific article published on 2 June 2010

Combined 1H-NMR and 1H-13C HSQC-NMR to improve urinary screening in autism spectrum disorders

scientific article published in July 2014

Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism

scientific article published on 21 July 2016

Comparative analysis of targeted metabolomics: dominance-based rough set approach versus orthogonal partial least square-discriminant analysis

scientific article published on 11 December 2014

Correction: 1H-NMR-Based Metabolomic Profiling of CSF in Early Amyotrophic Lateral Sclerosis.

scientific article published on 10 November 2010

Deficit in BDNF does not increase vulnerability to stress but dampens antidepressant-like effects in the unpredictable chronic mild stress.

scientific article

Disruption of TCA Cycle and Glutamate Metabolism Identified by Metabolomics in an In Vitro Model of Amyotrophic Lateral Sclerosis

scientific article published on 14 December 2015

Effect of familial clustering in the genetic screening of 235 French ALS families

scientific article published on 06 January 2021

Endogenous metabolites-mediated communication between OAT1/OAT3 and OATP1B1 may explain the association between SLCO1B1 SNPs and methotrexate toxicity.

scientific article

Erratum to "Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management" [Clin. Biochem. 49 (2016) 1047-1050]

scientific article published on 02 May 2017

Exclusion of the coding sequence of the doublecortin gene as a susceptibility locus in autistic disorder.

scientific article published in March 2002

Fate of inhaled monoclonal antibodies after the deposition of aerosolized particles in the respiratory system.

scientific article published on 17 October 2014

Fetal exposure to teratogens: evidence of genes involved in autism

scientific article

Filter paper saturated by urine sample in metabolic disorders detection by proton magnetic resonance spectroscopy

scientific article published on 25 November 2009

Further development of biomarkers in amyotrophic lateral sclerosis.

scientific article

GC-MS-based urine metabolic profiling of autism spectrum disorders.

scientific article published on 10 April 2013

Gabra5-gene haplotype block associated with behavioral properties of the full agonist benzodiazepine chlordiazepoxide.

scientific article published on 4 June 2012

Gastrointestinal symptoms resembling ulcerative proctitis caused by larvae of the drone fly Eristalis tenax

scientific article

Genetics of amyotrophic lateral sclerosis

article

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis

scientific article published on 25 July 2016

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation

scientific article

Homozygous SMN2 deletion is a protective factor in the Swedish ALS population

scientific article published on 25 January 2012

How Can a Ketogenic Diet Improve Motor Function?

scientific article published on 26 January 2018

Identification of metabolic pathway disturbances using multimodal metabolomics in autistic disorders in a Middle Eastern population

scientific article published on 29 January 2018

Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders

scientific article published on 29 June 2019

In ALS, a mutation could be worth two steps

scientific article published on 01 December 2018

Increased heart rate variability in mice overexpressing the Cu/Zn superoxide dismutase.

scientific article published on 23 April 2008

Inhibition of Pathogenic Mutant SOD1 Aggregation in Cultured Motor Neuronal Cells by Prevention of Its SUMOylation on Lysine 75.

scientific article published on 26 November 2015

Inhibition of β-Glucocerebrosidase Activity Preserves Motor Unit Integrity in a Mouse Model of Amyotrophic Lateral Sclerosis

scientific article published on 12 July 2017

Iron metabolism disturbance in a French cohort of ALS patients

scientific article

Is NMR metabolic profiling of spent embryo culture media useful to assist in vitro human embryo selection?

scientific article published on 10 August 2012

LIMK2d, a truncated isoform of Lim kinase 2 regulates neurite growth in absence of the LIM kinase domain

scientific article published on 3 March 2012

Lipidomics Reveals Cerebrospinal-Fluid Signatures of ALS.

scientific article published on 15 December 2017

Low IDL-B and high LDL-1 subfraction levels in serum of ALS patients

scientific article published on 18 July 2017

Low specificity of urinary 3-methoxytyramine in screening of dopamine-secreting pheochromocytomas and paragangliomas

scientific article published on 18 May 2016

Malnutrition at the time of diagnosis is associated with a shorter disease duration in ALS.

scientific article published on 31 July 2010

Management of the cutaneous reaction induced by scorpion sting: thinking about treatment and means of prevention

scientific article published on 09 February 2015

Maternal exposure to LPS induces hypomyelination in the internal capsule and programmed cell death in the deep gray matter in newborn rats

scientific article published in March 2006

Metabolomics Study of Urine in Autism Spectrum Disorders Using a Multiplatform Analytical Methodology

scientific article published on 5 November 2015

Metabolomics in Cerebrospinal Fluid of Patients with Amyotrophic Lateral Sclerosis: An Untargeted Approach via High-Resolution Mass Spectrometry

Metabolomics in amyotrophic lateral sclerosis: how far can it take us?

scientific article published on 29 January 2016

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

scientific article published in February 2003

Mutation in the RRM2 domain of TDP-43 in Amyotrophic Lateral Sclerosis with rapid progression associated with ubiquitin positive aggregates in cultured motor neurons.

scientific article published on 13 July 2017

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder

scientific article

Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism

scientific article published on 11 September 2015

Mutations of the ANG gene in French patients with sporadic amyotrophic lateral sclerosis

scientific article published on 01 October 2008

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity.

scientific article published on 9 May 2016

New sampling strategy using a Bayesian approach to assess iohexol clearance in kidney transplant recipients.

scientific article

No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients.

scientific article published in July 2001

Novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis.

scientific article

Oligodendrocyte myelin glycoprotein (OMgp): evolution, structure and function

scientific article published on 01 May 2004

Omics to Explore Amyotrophic Lateral Sclerosis Evolution: the Central Role of Arginine and Proline Metabolism

scientific article published on 2 September 2016

Panel of Oxidative Stress and Inflammatory Biomarkers in ALS: A Pilot Study.

scientific article published on 24 October 2016

Phenotypic and genotypic studies of ALS cases in ALS-SMA families

scientific article published on 01 March 2018

Preanalytical conditions of point-of-care testing in the intensive care unit are decisive for analysis reliability

scientific article published on 24 June 2016

Prevention of mutant SOD1 motoneuron degeneration by copper chelatorsin vitro

scientific article published in January 2000

Reactive astrocyte COX2-PGE2 production inhibits oligodendrocyte maturation in neonatal white matter injury

scientific article published on 30 August 2017

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

scientific article

Renal impairment and ischemic stroke risk assessment in patients with atrial fibrillation: the Loire Valley Atrial Fibrillation Project

scientific article published on 21 March 2013

Respiratory onset in an ALS family with L144F SOD1 mutation

scientific article published on 20 June 2010

Risk and Protective Factors in Autism Spectrum Disorders: A Case Control Study in the Lebanese Population

scientific article published on 31 August 2020

Roles of LIM kinases in central nervous system function and dysfunction

scientific article

Routine determination of GFR in renal transplant recipients by HPLC quantification of plasma iohexol concentrations and comparison with estimated GFR

scientific article published on 01 September 2012

SMN1 gene study in three families in which ALS and spinal muscular atrophy co-exist

scientific article published on 01 November 2002

SMN1 gene, but not SMN2, is a risk factor for sporadic ALS

article

SOD1 mutation can mask C9orf72 abnormal expansion

scientific article

Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results From the French National Paediatric Cohort CONAPE.

scientific article published on 7 November 2017

Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening

scientific article published on 01 July 2000

Specific Metabolome Profile of Exhaled Breath Condensate in Patients with Shock and Respiratory Failure: A Pilot Study.

scientific article published on September 2016

Study of the HFE gene common polymorphisms in French patients with sporadic amyotrophic lateral sclerosis

scientific article published on 14 March 2012

Study of the serotonin transporter (SLC6A4) and BDNF genes in French patients with non syndromic mental deficiency

scientific article

The BDNF Val(66)Met polymorphism is associated with escitalopram response in depressed patients

scientific article published on 31 July 2014

The Metabolic Disturbances of Motoneurons Exposed to Glutamate.

scientific article published on 12 February 2018

The P413L chromogranin B variation in French patients with sporadic amyotrophic lateral sclerosis

article

The combination of four analytical methods to explore skeletal muscle metabolomics: Better coverage of metabolic pathways or a marketing argument?

scientific article published on 18 October 2017

The oligodendrocyte-myelin glycoprotein gene is highly expressed during the late stages of myelination in the rat central nervous system.

scientific article published in September 2003

Total Protein Level in Cerebrospinal Fluid is Stable in Elderly Adults

scientific article published on 01 October 2013

Transgenic acetylcholinesterase induces enlargement of murine neuromuscular junctions but leaves spinal cord synapses intact

scientific article published on 01 May 1998

Transgenic expression of human acetylcholinesterase induces progressive cognitive deterioration in mice.

scientific article published in September 1995

Transmission disequilibrium study of an oligodendrocyte and myelin glycoprotein gene allele in 431 families with an autistic proband

scientific article published on 19 August 2007

Untargeted 1H-NMR metabolomics in CSF: toward a diagnostic biomarker for motor neuron disease

scientific article published on 28 February 2014

Ursodeoxycholic acid therapy in intrahepatic cholestasis of pregnancy: Results in real-world conditions and factors predictive of response to treatment.

scientific article published on 20 October 2016

Validation of amino-acids measurement in dried blood spot by FIA-MS/MS for PKU management.

scientific article published on 20 July 2016

Variability in creatinine excretion in adult diabetic, overweight men and women: consequences on creatinine-based classification of renal disease.

scientific article

Vitamin D is Not a Protective Factor in ALS.

scientific article published on 20 June 2015

Wildtype motoneurons, ALS-Linked SOD1 mutation and glutamate profoundly modify astrocyte metabolism and lactate shuttling.

scientific article published on 31 January 2017

Workflow methodology for rat brain metabolome exploration using NMR, LC-MS and GC-MS analytical platforms

scientific article published on 13 May 2017

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

scientific article

[Genetics of motor neuron disorders]

scientific article published on 20 February 2008

[Investigation of hyperhomocysteinemia].

scientific article

[Late onset Tay-Sachs disease may mimic adult SMA]

scientific article published on 08 April 2011

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