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D. Bichet · SciRah

Researcher profile · Semantic Scholar

D. Bichet

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D. Bichet — researcher profile on SciRah

h-index: 62
Works: 297
Citations: 15K

Most-cited papers

Special feature Clinical Practice Guideline on Diagnosis and Treatment of Hyponatraemia
G. Spasovski, R. Vanholder, B. Allolio, D. Annane +13 more
2015695 citations
Semantic Scholar
Treatment of Fabry's Disease with the Pharmacologic Chaperone Migalastat.
D. Germain, D. Hughes, K. Nicholls, D. Bichet +36 more
2016New England Journal of Medicine470 citations Open access
Semantic Scholar
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT study
D. Hughes, K. Nicholls, S. Shankar, G. Sunder-Plassmann +34 more
2016Journal of Medical Genetics348 citations Open access
Semantic Scholar
Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus
D. Bockenhauer, D. Bichet
2015Nature Reviews Nephrology287 citations
Semantic Scholar
The validation of pharmacogenetics for the identification of Fabry patients to be treated with migalastat
Elfrida R. Benjamin, M. C. Della Valle, Xiao-Yang Wu, Evan Katz +18 more
2016Genetics in Medicine204 citations Open access
Semantic Scholar
Time to treatment benefit for adult patients with Fabry disease receiving agalsidase β: data from the Fabry Registry
A. Ortiz, Ademola K. Abiose, D. Bichet, G. Cabrera +14 more
2016Journal of Medical Genetics144 citations Open access
Semantic Scholar
Vasopressin and hydration play a major role in the development of glucose intolerance and hepatic steatosis in obese rats
C. Taveau, Catherine Chollet, L. Waeckel, Dorinne Desposito +13 more
2015Diabetologia83 citations Open access
Semantic Scholar
MAP17 Is a Necessary Activator of Renal Na+/Glucose Cotransporter SGLT2.
M. Coady, Abdulah El Tarazi, R. Santer, P. Bissonnette +6 more
2017Journal of the American Society of Nephrology82 citations Open access
Semantic Scholar
Use of a rare disease registry for establishing phenotypic classification of previously unassigned GLA variants: a consensus classification system by a multispecialty Fabry disease genotype–phenotype workgroup
D. Germain, J. Oliveira, D. Bichet, H. Yoo +6 more
2020Journal of Medical Genetics70 citations Open access
Semantic Scholar
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).
D. Bichet, D. Bockenhauer
2016Best practice & research. Clinical endocrinology & metabolism70 citations
Semantic Scholar
Urinary biomarker investigation in children with Fabry disease using tandem mass spectrometry.
C. Auray-Blais, Catherine-Marie Blais, U. Ramaswami, Michel Boutin +10 more
2015Clinica chimica acta; international journal of clinical chemistry70 citations
Semantic Scholar
Total Kidney Volume in Autosomal Dominant Polycystic Kidney Disease: A Biomarker of Disease Progression and Therapeutic Efficacy.
Ahsan Alam, N. Dahl, J. Lipschutz, S. Rossetti +5 more
2015American Journal of Kidney Diseases68 citations
Semantic Scholar
Oral Migalastat HCl Leads to Greater Systemic Exposure and Tissue Levels of Active α-Galactosidase A in Fabry Patients when Co-Administered with Infused Agalsidase
D. Warnock, D. Bichet, M. Holida, O. Goker-Alpan +15 more
2015PLoS ONE64 citations Open access
Semantic Scholar
Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study
M. Arends, M. Biegstraaten, Christoph Wanner, S. Sirrs +12 more
2018Journal of Medical Genetics61 citations Open access
Semantic Scholar
Regulation of Thirst and Vasopressin Release.
D. Bichet
2019Annual Review of Physiology60 citations Open access
Semantic Scholar
Impaired Left Atrial Function in Fabry Disease: A Longitudinal Speckle‐Tracking Echocardiography Study
M. Pichette, K. Serri, M. Pagé, Lu-Zhao Di +2 more
2017Journal of the American Society of Echocardiography56 citations
Semantic Scholar
Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial
F. Wijburg, B. Bénichou, D. Bichet, L. Clarke +14 more
2015PLoS ONE55 citations Open access
Semantic Scholar
Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease
D. Bichet, J. Aerts, C. Auray-Blais, H. Maruyama +4 more
2020Genetics in Medicine50 citations Open access
Semantic Scholar
Vasopressin and the Regulation of Thirst
D. Bichet
2018Annals of Nutrition and Metabolism43 citations Open access
Semantic Scholar
Acute and chronic hyperglycemic effects of vasopressin in normal rats: involvement of V1A receptors.
C. Taveau, Catherine Chollet, D. Bichet, G. Velho +6 more
2017American Journal of Physiology. Endocrinology and Metabolism36 citations
Semantic Scholar
Hepatocyte Nuclear Factor-1β Regulates Urinary Concentration and Response to Hypertonicity.
Karam Aboudehen, Lama Noureddine, Patricia Cobo-Stark, Svetlana V. Avdulov +6 more
2017Journal of the American Society of Nephrology36 citations Open access
Semantic Scholar
Assessing Risk of Disease Progression and Pharmacological Management of Autosomal Dominant Polycystic Kidney Disease
S. Soroka, Ahsan Alam, M. Bevilacqua, L. Girard +6 more
2017Canadian Journal of Kidney Health and Disease35 citations Open access
Semantic Scholar
Long-term follow-up of renal function in patients treated with migalastat for Fabry disease
D. Bichet, R. Torra, E. Wallace, D. Hughes +6 more
2021Molecular Genetics and Metabolism Reports34 citations Open access
Semantic Scholar
Long-term multisystemic efficacy of migalastat on Fabry-associated clinical events, including renal, cardiac and cerebrovascular outcomes
D. Hughes, D. Bichet, R. Giugliani, R. Hopkin +9 more
2022Journal of Medical Genetics32 citations Open access
Semantic Scholar
Updated Canadian Expert Consensus on Assessing Risk of Disease Progression and Pharmacological Management of Autosomal Dominant Polycystic Kidney Disease
S. Soroka, Ahsan Alam, M. Bevilacqua, L. Girard +6 more
2018Canadian Journal of Kidney Health and Disease32 citations Open access
Semantic Scholar
Migalastat improves diarrhea in patients with Fabry disease: clinical-biomarker correlations from the phase 3 FACETS trial
R. Schiffmann, D. Bichet, A. Jovanović, D. Hughes +12 more
2018Orphanet Journal of Rare Diseases29 citations Open access
Semantic Scholar
Nephrogenic diabetes insipidus
D. Bockenhauer, D. Bichet
2017Current opinion in pediatrics29 citations Open access
Semantic Scholar
Long-term outcome in inherited nephrogenic diabetes insipidus
Sonia Sharma, E. Ashton, D. Iancu, M. Arthus +5 more
2018Clinical Kidney Journal27 citations Open access
Semantic Scholar
OVERTURE: A Worldwide, Prospective, Observational Study of Disease Characteristics in Patients With ADPKD
R. Perrone, Dorothee Oberdhan, J. Ouyang, D. Bichet +8 more
2023Kidney International Reports26 citations Open access
Semantic Scholar
Treatment and long-term outcome in primary nephrogenic diabetes insipidus.
S. Lopez-Garcia, M. Downie, Ji Soo Kim, O. Boyer +73 more
2020Nephrology, Dialysis and Transplantation22 citations Open access
Semantic Scholar
GENETICS IN ENDOCRINOLOGY Pathophysiology, diagnosis and treatment of familial nephrogenic diabetes insipidus.
D. Bichet
2020European Journal of Endocrinology22 citations Open access
Semantic Scholar
Tandem mass spectrometry analysis of urinary podocalyxin and podocin in the investigation of podocyturia in women with preeclampsia and Fabry disease patients.
Tristan Martineau, Michel Boutin, A. Côté, B. Maranda +2 more
2019Clinica chimica acta; international journal of clinical chemistry21 citations
Semantic Scholar
Severe bradyarrhythmia linked to left atrial dysfunction in Fabry disease—A cross‐sectional study
Lu-Zhao Di, M. Pichette, R. Nadeau, D. Bichet +1 more
2018Clinical Cardiology16 citations Open access
Semantic Scholar
Vasopressin at Central Levels and Consequences of Dehydration
D. Bichet
2016Annals of Nutrition and Metabolism16 citations Open access
Semantic Scholar
Vaptans or voluntary increased hydration to protect the kidney: how do they compare?
L. Bankir, D. Guerrot, D. Bichet
2021Nephrology, Dialysis and Transplantation15 citations
Semantic Scholar
Disease-linked mutations alter the stoichiometries of HCN-KCNE2 complexes
Yoann Lussier, Oliver Fürst, Eva Fortea, Marc-Antoine Leclerc +5 more
2019Scientific Reports14 citations Open access
Semantic Scholar
The migalastat GLP-HEK assay is the gold standard for determining amenability in patients with Fabry disease
R. Schiffmann, D. Bichet, Elfrida R. Benjamin, Xiao-Yang Wu +1 more
2019Molecular Genetics and Metabolism Reports12 citations Open access
Semantic Scholar
Mass Spectrometry Analysis of Globotriaosylsphingosine and Its Analogues in Dried Blood Spots
Michel Boutin, P. Lavoie, Margot Beaudon, Georges Kabala Ntumba +3 more
2023International Journal of Molecular Sciences10 citations Open access
Semantic Scholar
Independent Registries Are Cost-Effective Tools to Provide Mandatory Postauthorization Surveillance for Orphan Medicinal Products.
S. Sirrs, M. Arthus, D. Bichet, C. Rockman-Greenberg +7 more
2020Value in Health10 citations Open access
Semantic Scholar
Safety of switching to Migalastat from enzyme replacement therapy in Fabry disease: Experience from the Phase 3 ATTRACT study
D. Hughes, K. Nicholls, G. Sunder-Plassmann, A. Jovanović +9 more
2019American Journal of Medical Genetics. Part A10 citations Open access
Semantic Scholar
Functional Recovery of AQP2 Recessive Mutations Through Hetero-Oligomerization with Wild-Type Counterpart
Abdulah El Tarazi, Yoann Lussier, Sandra Da Cal, P. Bissonnette +1 more
2016Scientific Reports10 citations Open access
Semantic Scholar
Analysis of globotriaosylceramide (Gb3) isoforms/analogs in unfractionated leukocytes, B lymphocytes and monocytes from Fabry patients using ultra-high performance liquid chromatography/tandem mass spectrometry.
Amanda Toupin, P. Lavoie, M. Arthus, Mona Abaoui +5 more
2018Analytica Chimica Acta9 citations
Semantic Scholar
Vasopressin Use in the Support of Organ Donors: Physiological Rationale and Review of the Literature
Sofiane Ouerd, A. Frenette, D. Williamson, K. Serri +3 more
2023Critical Care Explorations8 citations Open access
Semantic Scholar
Mice deficient for ERAD machinery component Sel1L develop central diabetes insipidus.
D. Bichet, Yoann Lussier
2017Journal of Clinical Investigation8 citations Open access
Semantic Scholar
Water and Sodium Balance
C. Ichai, D. Bichet
20187 citations
Semantic Scholar
SP004EFFECTS OF LONG-TERM MIGALASTAT TREATMENT ON RENAL FUNCTION BY BASELINE PROTEINURIA IN PATIENTS (PTS) WITH FABRY DISEASE
R. Schiffmann, D. Bichet, D. Germain, R. Giugliani +8 more
20187 citations Open access
Semantic Scholar
What can copeptin tell us in patients with autosomal dominant polycystic disease?
L. Bankir, D. Bichet
2019Kidney International6 citations Open access
Semantic Scholar
Vasopressin and oxytocin receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
D. Bichet, M. Bouvier, B. Chini, G. Gimpl +12 more
2019IUPHAR/BPS Guide to Pharmacology CITE6 citations Open access
Semantic Scholar
The Posterior Pituitary
D. Bichet
20176 citations
Semantic Scholar
The Safety of Agalsidase Alfa Enzyme Replacement Therapy in Canadian Patients with Fabry Disease Following Implementation of a Bioreactor Process
Aneal Khan, S. Sirrs, D. Bichet, Chantal F. Morel +3 more
2021Drugs in R&D5 citations Open access
Semantic Scholar

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