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K. Dahan · SciRah

Researcher profile · Semantic Scholar

K. Dahan

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K. Dahan — researcher profile on SciRah

h-index: 47
Works: 180
Citations: 10K

Most-cited papers

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor, H. Martin, S. Lise, J. Broxholme +106 more
2015Nature Genetics389 citations Open access
Semantic Scholar
Rituximab for Severe Membranous Nephropathy: A 6-Month Trial with Extended Follow-Up.
K. Dahan, H. Dębiec, E. Plaisier, M. Cachanado +9 more
2017Journal of the American Society of Nephrology372 citations Open access
Semantic Scholar
Autosomal dominant tubulointerstitial kidney disease: diagnosis, classification, and management--A KDIGO consensus report.
K. Eckardt, S. Alper, C. Antignac, A. Bleyer +9 more
2015Kidney International318 citations Open access
Semantic Scholar
Long-term efficacy and safety of rituximab in IgG4-related disease: Data from a French nationwide study of thirty-three patients
M. Ebbo, A. Grados, M. Samson, M. Groh +25 more
2017PLoS ONE218 citations Open access
Semantic Scholar
Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844–848
Magdalena Koczkowska, Yun-Jia Chen, T. Callens, Alicia Gomes +71 more
2017American Journal of Human Genetics196 citations Open access
Semantic Scholar
Improving mutation screening in familial hematuric nephropathies through next generation sequencing.
V. Moriniére, K. Dahan, P. Hilbert, M. Lison +12 more
2014Journal of the American Society of Nephrology159 citations Open access
Semantic Scholar
Evidence of digenic inheritance in Alport syndrome
M. Mencarelli, L. Heidet, H. Storey, M. van Geel +16 more
2015Journal of Medical Genetics158 citations Open access
Semantic Scholar
Genetic testing in the diagnosis of chronic kidney disease: recommendations for clinical practice
N. Knoers, C. Antignac, C. Bergmann, K. Dahan +7 more
2021Nephrology, Dialysis and Transplantation153 citations Open access
Semantic Scholar
Rituximab is an efficient and safe treatment in adults with steroid-dependent minimal change disease.
H. Munyentwali, Khedidja Bouachi, V. Audard, P. Rémy +6 more
2013Kidney International141 citations Open access
Semantic Scholar
Anti TNF-α in refractory Takayasu's arteritis: cases series and review of the literature.
C. Comarmond, E. Plaisier, K. Dahan, T. Mirault +4 more
2012Autoimmunity Reviews138 citations
Semantic Scholar
B- and T-cell subpopulations in patients with severe idiopathic membranous nephropathy may predict an early response to rituximab.
M. Rosenzwajg, Eva Languille, H. Dębiec, Joana Hygino +4 more
2017Kidney International130 citations Open access
Semantic Scholar
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome
P. J. van der Sluijs, S. Jansen, S. Vergano, Miho Adachi-Fukuda +101 more
2018Genetics in Medicine125 citations Open access
Semantic Scholar
Clinical and Genetic Spectra of Autosomal Dominant Tubulointerstitial Kidney Disease due to Mutations in UMOD and MUC1.
E. Olinger, P. Hofmann, K. Kidd, I. Dufour +29 more
2020Kidney International124 citations Open access
Semantic Scholar
High-Dose Rituximab and Early Remission in PLA2R1-Related Membranous Nephropathy.
B. Seitz-Polski, K. Dahan, H. Dębiec, A. Rousseau +9 more
2019American Society of Nephrology. Clinical Journal118 citations Open access
Semantic Scholar
Phospholipase A2 Receptor 1 Epitope Spreading at Baseline Predicts Reduced Likelihood of Remission of Membranous Nephropathy.
B. Seitz-Polski, H. Dębiec, A. Rousseau, K. Dahan +5 more
2017Journal of the American Society of Nephrology107 citations Open access
Semantic Scholar
NPHS2 Mutations in Steroid‐Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum
K. Bouchireb, O. Boyer, O. Gribouval, F. Névo +21 more
2014Human Mutation94 citations Open access
Semantic Scholar
Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
E. Ashton, A. Legrand, V. Benoit, Isabelle Roncelin +16 more
2018Kidney International92 citations Open access
Semantic Scholar
Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1
L. Mansour-Hendili, A. Blanchard, Nelly Le Pottier, Isabelle Roncelin +64 more
2015Human Mutation85 citations Open access
Semantic Scholar
Prognostic value of PLA2R autoimmunity detected by measurement of anti-PLA2R antibodies combined with detection of PLA2R antigen in membranous nephropathy: A single-centre study over 14 years
Franck Pourcine, K. Dahan, Fabrice Mihout, M. Cachanado +3 more
2017PLoS ONE74 citations Open access
Semantic Scholar
Report of the Inefficacy of Eculizumab in Two Cases of Severe Antibody-Mediated Rejection of Renal Grafts
M. Burbach, C. Suberbielle, I. Brocheriou, C. Ridel +4 more
2014Transplantation71 citations Open access
Semantic Scholar
Immunological remission in PLA2R-antibody-associated membranous nephropathy: cyclophosphamide versus rituximab.
A. van de Logt, K. Dahan, A. Rousseau, R. G. van der Molen +3 more
2018Kidney International70 citations Open access
Semantic Scholar
An Augmented ABCA4 Screen Targeting Noncoding Regions Reveals a Deep Intronic Founder Variant in Belgian Stargardt Patients
M. Bauwens, J. de Zaeytijd, N. Weisschuh, S. Kohl +10 more
2015Human Mutation70 citations
Semantic Scholar
Constitutional mismatch repair deficiency–associated brain tumors: report from the European C4CMMRD consortium
L. Guerrini-Rousseau, P. Varlet, C. Colas, F. Andreiuolo +16 more
2019Neuro-Oncology Advances61 citations Open access
Semantic Scholar
Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome
H. Belge, K. Dahan, J. Cambier, V. Benoit +5 more
2016Nephrology, Dialysis and Transplantation50 citations Open access
Semantic Scholar
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes
R. Gallon, Barbara Mühlegger, Sören-Sebastian Wenzel, H. Sheth +31 more
2019Human Mutation48 citations Open access
Semantic Scholar
High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
M. Hureaux, E. Ashton, K. Dahan, P. Houillier +15 more
2019Kidney International48 citations Open access
Semantic Scholar
Recurrent FXYD2 p.Gly41Arg mutation in patients with isolated dominant hypomagnesaemia.
J. de Baaij, E. Dorresteijn, Eric Hennekam, E. Kamsteeg +8 more
2015Nephrology, Dialysis and Transplantation48 citations Open access
Semantic Scholar
Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome
G. Dorval, O. Gribouval, Vanesa Martínez-Barquero, Eduardo Machuca +46 more
2018Pediatric nephrology (Berlin, West)41 citations
Semantic Scholar
Functional classification of ATM variants in ataxia‐telangiectasia patients
A. Fiévet, D. Bellanger, Guillaume Rieunier, C. Dubois d'Enghien +42 more
2019Human Mutation39 citations Open access
Semantic Scholar
Evidence of follicular T-cell implication in a case of IgG4-related systemic disease with interstitial nephritis.
M. Zaidan, P. Cervera-Pierot, S. de Seigneux, K. Dahan +4 more
2011Nephrology, Dialysis and Transplantation39 citations
Semantic Scholar
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy
Karl-Peter Schlingmann, F. Jouret, Kuang Shen, A. Nigam +32 more
2021Journal of the American Society of Nephrology38 citations Open access
Semantic Scholar
Rituximab in Patients With Phospholipase A2 Receptor–Associated Membranous Nephropathy and Severe CKD
N. Hanset, Emmanuel Esteve, E. Plaisier, C. Johanet +7 more
2019Kidney International Reports38 citations Open access
Semantic Scholar
Genotype and Outcome After Kidney Transplantation in Alport Syndrome
V. Gillion, K. Dahan, J. Cosyns, P. Hilbert +7 more
2018Kidney International Reports38 citations Open access
Semantic Scholar
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
L. Claus, Chuan Chen, Jennifer L. Stallworth, Joshu Turner +43 more
2023Kidney International36 citations Open access
Semantic Scholar
Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes
J. Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, A. Dias +65 more
2022The Lancet Oncology35 citations Open access
Semantic Scholar
Eculizumab in Anti-Factor H Antibodies Associated With Atypical Hemolytic Uremic Syndrome
Benedetta Diamante Chiodini, J. Davin, F. Corazza, Karim Khaldi +3 more
2014Pediatrics33 citations Open access
Semantic Scholar
High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers
Maribel González-Acosta, F. Marín, Benjamin R. Puliafito, N. Bonifaci +31 more
2019Journal of Medical Genetics31 citations Open access
Semantic Scholar
Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies
A. Werion, P. Storms, Ysaline Zizi, C. Beguin +13 more
2023American Society of Nephrology. Clinical Journal30 citations Open access
Semantic Scholar
Constitutional microsatellite instability, genotype, and phenotype correlations in Constitutional Mismatch Repair Deficiency.
R. Gallon, R. Phelps, Christine Hayes, L. Brugières +43 more
2022Gastroenterology27 citations Open access
Semantic Scholar
Efficacy and Safety of Rituximab in Hepatitis B Virus–Associated PLA2R-Positive Membranous Nephropathy
Lena Berchtold, G. Zanetta, K. Dahan, Fabrice Mihout +5 more
2017Kidney International Reports27 citations Open access
Semantic Scholar
Gitelman syndrome and glomerular proteinuria: a link between loss of sodium-chloride cotransporter and podocyte dysfunction?
N. Demoulin, S. Aydın, J. Cosyns, K. Dahan +4 more
2014Nephrology, Dialysis and Transplantation22 citations Open access
Semantic Scholar
Apixaban Prophylactic Anticoagulation in Patients with Nephrotic Syndrome
T. Van Meerhaeghe, Alexandre Cez, K. Dahan, Emmanuel Esteve +3 more
2021TH Open21 citations Open access
Semantic Scholar
Paradoxical response to furosemide in uromodulin-associated kidney disease.
L. Labriola, E. Olinger, H. Belge, Y. Pirson +2 more
2015Nephrology, Dialysis and Transplantation21 citations Open access
Semantic Scholar
The Role of PLA2R Antibody in Treatment of Membranous Nephropathy
K. Dahan, V. Gillion, C. Johanet, H. Dębiec +1 more
2017Kidney International Reports20 citations Open access
Semantic Scholar
Early-onset of ADCK4 glomerulopathy with renal failure: a case report
K. Lolin, B. Chiodini, E. Hennaut, B. Adams +2 more
2017BMC Medical Genetics19 citations Open access
Semantic Scholar
Urinary mRNA for the Diagnosis of Renal Allograft Rejection: The Issue of Normalization
P. Galichon, L. Amrouche, A. Hertig, I. Brochériou +8 more
2016American Journal of Transplantation18 citations Open access
Semantic Scholar
Membranous Nephropathy Associated With Immunological Disorder-Related Liver Disease
M. Dauvergne, A. Moktefi, M. Rabant, C. Vigneau +20 more
2015Medicine18 citations Open access
Semantic Scholar
Belgian consensus statement on the diagnosis and management of patients with atypical hemolytic uremic syndrome
K. Claes, A. Massart, L. Collard, L. Weekers +19 more
2018Acta Clinica Belgica17 citations Open access
Semantic Scholar
Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families
A. Renault, N. Mebirouk, Eve Cavaciuti, Dorothée Le Gal +26 more
2017Carcinogenesis17 citations Open access
Semantic Scholar
Survival and specific outcome of sickle cell disease patients after renal transplantation
C. Gérardin, A. Moktefi, C. Couchoud, A. Duquesne +19 more
2019British Journal of Haematology16 citations Open access
Semantic Scholar

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