J.-J Martin - Related publications

Affiliations: 
Universiteit Antwerpen (Belgium) 
Area:
Mental Health, Cognitive Psychology, Psychometrics Psychology
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2020 McClatchey MA, du Toit ZD, Vaughan R, Whatley SD, Martins S, Hegde S, Naude JTW, Thomas DH, Griffiths DF, Research Consortium GE, Clarke AJ, Fry AE. Focal segmental glomerulosclerosis and mild intellectual disability in a patient with a novel de novo truncating TRIM8 mutation. European Journal of Medical Genetics. 103972. PMID 32531461 DOI: 10.1016/j.ejmg.2020.103972   
2020 Lim SH, Kim JH, Han KH, Ahn YH, Kang HG, Ha IS, Cheong HI. Genotype and Phenotype Analyses in Pediatric Patients with Mutations. Journal of Clinical Medicine. 9. PMID 32708349 DOI: 10.3390/jcm9072320   
2020 Rahmani F, Rayzan E, Rahmani MR, Shahkarami S, Zoghi S, Rezaei A, Aryan Z, Najafi M, Rohlfs M, Jeske T, Aflatoonian M, Chavoshzadeh Z, Farahmand F, Motamed F, Rohani P, et al. Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR). Immunological Investigations. 1-15. PMID 32633164 DOI: 10.1080/08820139.2020.1776725   
2020 Kotan D, Özözen Ayas Z, Tunca C, Gungen BD, Akçimen F, Başak AN. Phenotypic and genotypic features of patients diagnosed with ALS in the city of Sakarya, Turkey. Acta Neurologica Belgica. PMID 32671691 DOI: 10.1007/s13760-020-01441-z   
2020 Martínez de LaPiscina I, Hernández-Ramírez LC, Portillo N, Gómez-Gila AL, Urrutia I, Martínez-Salazar R, García-Castaño A, Aguayo A, Rica I, Gaztambide S, Faucz FR, Keil MF, Lodish MB, Quezado M, Pankratz N, et al. Rare Germline Variants in Pediatric Patients With Cushing's Disease: What Is Their Role? Frontiers in Endocrinology. 11: 433. PMID 32714280 DOI: 10.3389/fendo.2020.00433   
2020 Okada T, Washida K, Irie K, Saito S, Noguchi M, Tomita T, Koga M, Toyoda K, Okazaki S, Koizumi T, Mizuta I, Mizuno T, Ihara M. Prevalence and Atypical Clinical Characteristics of Mutations Among Patients Admitted for Acute Lacunar Infarctions. Frontiers in Aging Neuroscience. 12: 130. PMID 32477100 DOI: 10.3389/fnagi.2020.00130   
2020 Kimonis V, Al Dubaisi R, Maclean AE, Hall K, Weiss L, Stover AE, Schwartz PH, Berg B, Cheng C, Parikh S, Conner BR, Wu S, Hasso AN, Scott DA, Koenig MK, et al. mitochondrial disease: new patients and review of the genetic and clinical spectrum. Journal of Medical Genetics. PMID 32518176 DOI: 10.1136/jmedgenet-2020-106846   
2020 Lin J, Chen W, Huang P, Xie Y, Zheng M, Yao X. The distinct manifestation of young-onset amyotrophic lateral sclerosis in China. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-8. PMID 32729724 DOI: 10.1080/21678421.2020.1797091   
2020 Molnár MJ, Borsos B, Várdi KV, Grosz Z, Sebők Á, Dézsi L, Almássy Z, Kerényi L, Jobbágy Z, Jávor L, Bidló J. [The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. Ideggyogyaszati Szemle. 73: 151-159. PMID 32579304 DOI: 10.18071/isz.73.0151   
2020 Ohno S, Ozawa J, Fukuyama M, Makiyama T, Horie M. An NGS-based genotyping in LQTS; minor genes are no longer minor. Journal of Human Genetics. PMID 32681117 DOI: 10.1038/s10038-020-0805-z   
2020 Lu Y, Sun K, Guo S, Wang J, Li A, Rong X, Wang T, Shang Y, Chang W, Wang S. Early Warning Indicators of Severe COVID-19: A Single-Center Study of Cases From Shanghai, China. Frontiers in Medicine. 7: 432. PMID 32766268 DOI: 10.3389/fmed.2020.00432   
2020 Turan H, Dağdeviren Çakır A, Özer Y, Tarçın G, Özcabi B, Ceylaner S, Ercan O, Evliyaoğlu SO. Clinical and genetic characteristics of patients with corticosterone methyloxidase deficiency type 2: Novel mutations in . Journal of Clinical Research in Pediatric Endocrinology. PMID 32539318 DOI: 10.4274/jcrpe.galenos.2020.2019.0216   
2020 Chen SJ, Lee BC, Lee NC, Chien YH, Hwu WL, Lin CH. Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 32643304 DOI: 10.1002/ajmg.b.32810   
2020 Aardoom MA, Kemos P, Tindemans I, Aloi M, Koletzko S, Levine A, Turner D, Veereman G, Neyt M, Russell RK, Walters TD, Ruemmele FM, Samsom JN, Croft NM, de Ridder L, , et al. International prospective observational study investigating the disease course and heterogeneity of paediatric-onset inflammatory bowel disease: the protocol of the PIBD-SETQuality inception cohort study. Bmj Open. 10: e035538. PMID 32611739 DOI: 10.1136/bmjopen-2019-035538   
2020 Mueller C, Berry JD, McKenna-Yasek DM, Gernoux G, Owegi MA, Pothier LM, Douthwright CL, Gelevski D, Luppino SD, Blackwood M, Wightman NS, Oakley DH, Frosch MP, Flotte TR, Cudkowicz ME, et al. Suppression with Adeno-Associated Virus and MicroRNA in Familial ALS. The New England Journal of Medicine. 383: 151-158. PMID 32640133 DOI: 10.1056/NEJMoa2005056   
2020 Kang LL, Liu YP, Shen M, Chen ZH, Song JQ, He RX, Liu Y, Zhang Y, Dong H, Li MQ, Jin Y, Zheng H, Wang Q, Ding Y, Li XY, et al. [The phenotypes and genotypes in 314 patients with isolated methylmalonic acidemia]. Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics. 58: 468-475. PMID 32521958 DOI: 10.3760/cma.j.cn112140-20200401-00339   
2020 Zhao J, Gao HY, Feng ZY, Wu QJ. A Retrospective Analysis of the Clinical and Epidemiological Characteristics of COVID-19 Patients in Henan Provincial People's Hospital, Zhengzhou, China. Frontiers in Medicine. 7: 286. PMID 32582740 DOI: 10.3389/fmed.2020.00286   
2020 Oliveira Santos M, Gromicho M, Pinto S, De Carvalho M. Clinical characteristics in young-adult ALS - results from a Portuguese cohort study. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-4. PMID 32654518 DOI: 10.1080/21678421.2020.1790611   
2020 Wan Y, Wang Y, Fang F, Wu G, Zhang M. Mutations in the exons of epidermal growth factor receptor gene are associated with clinicopathological features of lung cancer. Asian Journal of Surgery. PMID 32747142 DOI: 10.1016/j.asjsur.2020.06.015   
2020 Blincoe A, Heeg M, Campbell PK, Hines M, Khojah A, Klein-Gitelman M, Talano JA, Speckmann C, Touzot F, Lankester A, Legger GE, Rivière JG, Garcia-Prat M, Alonso L, Putti MC, et al. Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis. Journal of Clinical Immunology. PMID 32638196 DOI: 10.1007/s10875-020-00814-6   
2020 Liu J, Yang H, Xu X, Yi S, Meng L. Mutations in the BCR-ABL1 kinase domain in patients with chronic myeloid leukaemia treated with TKIs or at diagnosis. Oncology Letters. 20: 1071-1076. PMID 32724345 DOI: 10.3892/ol.2020.11650   
2020 Vera G, Sorlin A, Delplancq G, Lecoquierre F, Brasseur-Daudruy M, Petit F, Smol T, Ziegler A, Bonneau D, Colin E, Mercier S, Cogné B, Bézieau S, Edery P, Lesca G, et al. Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND). European Journal of Medical Genetics. 104004. PMID 32688057 DOI: 10.1016/j.ejmg.2020.104004   
2020 Haug N, Deischinger C, Gyimesi M, Kautzky-Willer A, Thurner S, Klimek P. High-risk multimorbidity patterns on the road to cardiovascular mortality. Bmc Medicine. 18: 44. PMID 32151252 DOI: 10.1186/s12916-020-1508-1   
2020 Kim CY, Wirth T, Hubsch C, Németh AH, Okur V, Anheim M, Drouot N, Tranchant C, Rudolf G, Chelly J, Tatton-Brown K, Blauwendraat C, Vonsattel JPG, Cortes E, Alcalay RN, et al. Early-onset parkinsonism is a manifestation of the PPP2R5D p.E200K mutation. Annals of Neurology. PMID 32743835 DOI: 10.1002/ana.25863   
2020 Park E, Lee C, Kim NKD, Ahn YH, Park YS, Lee JH, Kim SH, Cho MH, Cho H, Yoo KH, Shin JI, Kang HG, Ha IS, Park WY, Cheong HI. Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis. Journal of Clinical Medicine. 9. PMID 32604935 DOI: 10.3390/jcm9062013   
2020 Sánchez-Valle J, Tejero H, Fernández JM, Juan D, Urda-García B, Capella-Gutiérrez S, Al-Shahrour F, Tabarés-Seisdedos R, Baudot A, Pancaldi V, Valencia A. Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships. Nature Communications. 11: 2854. PMID 32504002 DOI: 10.1038/s41467-020-16540-x   
2020 Samukawa M, Nakamura N, Hirano M, Morikawa M, Sakata H, Nishino I, Izumi R, Suzuki N, Kuroda H, Shiga K, Saigoh K, Aoki M, Kusunoki S. Neutral Lipid Storage Disease Associated with the PNPLA2 Gene: Case Report and Literature Review. European Neurology. 1-6. PMID 32564019 DOI: 10.1159/000508346   
2020 Deng X, Liu B, Li J, Zhang J, Zhao Y, Xu K. Blood biochemical characteristics of patients with coronavirus disease 2019 (COVID-19): a systemic review and meta-analysis. Clinical Chemistry and Laboratory Medicine. PMID 32554832 DOI: 10.1515/cclm-2020-0338   
2020 Kato A, Kamata M, Ito M, Uchida H, Nagata M, Fukaya S, Hayashi K, Fukuyasu A, Tanaka T, Ishikawa T, Ohnishi T, Tada Y. Higher baseline serum lactate dehydrogenase level is associated with poor effectiveness of dupilumab in the long term in patients with atopic dermatitis. The Journal of Dermatology. PMID 32548920 DOI: 10.1111/1346-8138.15464   
2020 Chen Y, Huang H, He Y, Chen M, Seidler U, Tian D, Xiao F. A20 Haploinsufficiency in a Chinese Patient With Intestinal Behcet's Disease-Like Symptoms: A Case Report. Frontiers in Immunology. 11: 1414. PMID 32719680 DOI: 10.3389/fimmu.2020.01414   
2020 Soveizi M, Mahdieh N, Setoodeh A, Sayarifard F, Abbasi F, Bose HS, Rabbani B, Rabbani A. p.Gln318X and p.Val281Leu as the Major Variants of Gene in Children with Idiopathic Premature Pubarche. International Journal of Endocrinology. 2020: 4329791. PMID 32714392 DOI: 10.1155/2020/4329791   
2020 Wu P, Chen S, Wu B, Chen J, Lv G. A Gene Mutation c.2395G>A Leads to TYK2 Deficiency: A Case Report and Literature Review. Frontiers in Pediatrics. 8: 253. PMID 32537443 DOI: 10.3389/fped.2020.00253   
2020 Ding Y, Yu L, Zhou S, Zhang L. Clinical Characteristic Analysis of Seven Children With Bickerstaff Brainstem Encephalitis in China. Frontiers in Neurology. 11: 557. PMID 32655484 DOI: 10.3389/fneur.2020.00557   
2020 Serratrice C, Stirnemann J, Berrahal A, Belmatoug N, Camou F, Caillaud C, Billette de Villemeur T, Dalbies F, Cador B, Froissart R, Masseau A, Brassier A, Hivert B, Swiader L, Bertchansky I, et al. A Cross-Sectional Retrospective Study of Non-Splenectomized and Never-Treated Patients with Type 1 Gaucher Disease. Journal of Clinical Medicine. 9. PMID 32708003 DOI: 10.3390/jcm9082343   
2020 Sha Y, Wei X, Ding L, Ji Z, Mei L, Huang X, Su Z, Wang W, Zhang X, Lin S. Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype. Journal of Human Genetics. PMID 32555313 DOI: 10.1038/s10038-020-0790-2   
2020 Dabas G, Mahajan R, De D, Handa S, Kumar R, Dayal D, Suthar R, Panigrahi I. Managing syndromic congenital ichthyosis at a tertiary care institute - Genotype-phenotype correlations, and novel treatments. Dermatologic Therapy. e13816. PMID 32533806 DOI: 10.1111/dth.13816   
2020 Jouali F, El Ansari FZ, Marchoudi N, Barakat A, Zmaimita H, Samlali H, Fekkak J. , , and genetic profile in Moroccan triple negative breast cancer cases. International Journal of Molecular Epidemiology and Genetics. 11: 16-25. PMID 32714499   
2020 Zhang LL, Cao XX, Shen KN, Han HX, Zhang CL, Qiu Y, Zhao H, Gao XM, Feng J, Zhang L, Zhou DB, Li J. Clinical characteristics and treatment outcome of type I cryoglobulinemia in Chinese patients: a single-center study of 45 patients. Annals of Hematology. PMID 32535708 DOI: 10.1007/s00277-020-04123-1   
2020 Bernard E, Nannya Y, Hasserjian RP, Devlin SM, Tuechler H, Medina-Martinez JS, Yoshizato T, Shiozawa Y, Saiki R, Malcovati L, Levine MF, Arango JE, Zhou Y, Solé F, Cargo CA, et al. Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes. Nature Medicine. PMID 32747829 DOI: 10.1038/s41591-020-1008-z   
2020 Chiusole B, Le Cesne A, Rastrelli M, Maruzzo M, Lorenzi M, Cappellesso R, Del Fiore P, Imbevaro S, Sbaraglia M, Terrier P, Ruggieri P, Dei Tos AP, Rossi CR, Zagonel V, Brunello A. Extraskeletal Myxoid Chondrosarcoma: Clinical and Molecular Characteristics and Outcomes of Patients Treated at Two Institutions. Frontiers in Oncology. 10: 828. PMID 32612944 DOI: 10.3389/fonc.2020.00828   
2020 Hayase T, Saito S, Shioda Y, Imamura T, Watanabe K, Ohki K, Yoshioka T, Oh Y, Kawahara Y, Niijima H, Imashuku S, Morimoto A. Analysis of the BRAF and MAP2K1 mutations in patients with Langerhans cell histiocytosis in Japan. International Journal of Hematology. PMID 32654047 DOI: 10.1007/s12185-020-02940-8   
2020 Wan Y, Wu J, Ni L, Luo Q, Yuan C, Fan F, Liu H, Zhang C, Xiang Y, Xie Q. Prognosis analysis of patients with mental disorders with COVID-19: a single-center retrospective study. Aging. 12. PMID 32561692 DOI: 10.18632/aging.103371   
2020 Chougar L, Shor N, Weiss N, Galanaud D, Leclercq D, Mathon B, Belkacem S, Stroër S, Burrel S, Boutolleau D, Demoule A, Rosso C, Delorme C, Seilhean D, Dormont D, ... , et al. Retrospective Observational Study of Brain Magnetic Resonance Imaging Findings in Patients with Acute SARS-CoV-2 Infection and Neurological Manifestations. Radiology. 202422. PMID 32677875 DOI: 10.1148/radiol.2020202422   
2020 Yang X, Kong J, Yang MX, Xie WP, Wang H, Rong R, Kong H. [Analysis of clinical characteristics of 21 cases of acute fibrinous and organizing pneumonia]. Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases. 43: 670-676. PMID 32727179 DOI: 10.3760/cma.j.cn112147-20191014-00685   
2020 Oppliger Leibundgut E, Haubitz M, Burington B, Ottmann OG, Spitzer G, Odenike O, McDevitt MA, Röth A, Snyder DS, Baerlocher GM. Dynamics of mutations in patients with essential thrombocythemia treated with imetelstat. Haematologica. PMID 32732354 DOI: 10.3324/haematol.2020.252817   
2020 Tian S, Chang Z, Wang Y, Wu M, Zhang W, Zhou G, Zou X, Tian H, Xiao T, Xing J, Chen J, Han J, Ning K, Wu T. Clinical Characteristics and Reasons for Differences in Duration From Symptom Onset to Release From Quarantine Among Patients With COVID-19 in Liaocheng, China. Frontiers in Medicine. 7: 210. PMID 32574322 DOI: 10.3389/fmed.2020.00210   
2020 Miguez ACK, Barros BDF, de Souza JES, da Costa CML, Cunha IW, Barbosa PNVP, Apezzato MLP, de Souza SJ, Carraro DM. Assessment of somatic mutations in urine and plasma of Wilms tumor patients. Cancer Medicine. PMID 32592321 DOI: 10.1002/cam4.3236   
2020 Zhang B, Zhou X, Zhu C, Song Y, Feng F, Qiu Y, Feng J, Jia Q, Song Q, Zhu B, Wang J. Immune Phenotyping Based on the Neutrophil-to-Lymphocyte Ratio and IgG Level Predicts Disease Severity and Outcome for Patients With COVID-19. Frontiers in Molecular Biosciences. 7: 157. PMID 32719810 DOI: 10.3389/fmolb.2020.00157   
2020 Cai Y, Wang Y, Sun J, Wang X, Xu Y, Sun C, Guo Y, Sun M, Ma K. Successful treatment of a patient with NSCLC carrying uncommon compound EGFR G719X and S768I mutations using osimertinib: A case report. The Journal of International Medical Research. 48: 300060520928793. PMID 32493093 DOI: 10.1177/0300060520928793   
2020 Sun Y, Wu C, Liu C, Shao Z. Dose-Reduced Decitabine Might Bring Benefits for Elderly AML Patients with Complex Karyotype: a Case Report. Clinical Laboratory. 66. PMID 32658429 DOI: 10.7754/Clin.Lab.2020.191224