Abdul Mueed Bidchol, PhD 个人学术档案

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	总计	2019 年至今
引用	422	226
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i10 指数	9	5

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Girisha KMProfessor of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher在 manipal.edu 的电子邮件经过验证
Hitesh ShahDepartment of Orthopaedics, Kasturba Medical College, Manipal Academy of Higher Education, Manipal在 manipal.edu 的电子邮件经过验证
Padma Priya TogarratiStaff Scientist, Blood Systems Research Institute在 bloodsystems.org 的电子邮件经过验证
Dr Debashish DandaProfessor & Founder of the Department of Clinical Immunology & Rheumatology, Christian Medical在 cmcvellore.ac.in 的电子邮件经过验证
Ashwin DalalHead, Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad在 cdfd.org.in 的电子邮件经过验证
Davor LesselUniversity Hospital Salzburg在 salk.at 的电子邮件经过验证
Stefan MundlosInstitut für Medizinische Genetik und Humangenetik, Charité在 molgen.mpg.de 的电子邮件经过验证
WILLIAM NEWMANProfessor of Translational Genomic Medicine, University of Manchester在 manchester.ac.uk 的电子邮件经过验证
Kapaettu SatyamoorthyShri Dharmasthala Manjunatheshwara University
Amit Kumar GuptaTeam Lead and Principal Research Engineer在 cisra.canon.com.au 的电子邮件经过验证

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Abdul Mueed Bidchol, PhD

Clinical Scientist-HOD

在 drsulaimanalhabib.com 的电子邮件经过验证

Molecular Genetics Lab Genetics of Mendelian Diseases NGS analysis Interpretation and reporting


标题按引用次数排序按年份排序按标题排序	引用次数引用次数	年份
Free radical scavenging activity of aqueous and ethanolic extract of Brassica oleracea L. var. italica AM Bidchol, A Wilfred, P Abhijna, R Harish Food and bioprocess technology 4 (7), 1137-1143, 2011	184	2011
Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia A Dalal, SL Bhavani G, PP Togarrati, T Bierhals, MR Nandineni, S Danda, ... American Journal of Medical Genetics Part A 158 (11), 2820-2828, 2012	80	2012
GALNS mutations in Indian patients with mucopolysaccharidosis IVA AM Bidchol, A Dalal, H Shah, S Nampoothiri, M Kabra, N Gupta, S Danda, ... American Journal of Medical Genetics Part A 164 (11), 2793-2801, 2014	43	2014
Recurrent and novel GLB1 mutations in India AM Bidchol, A Dalal, R Trivedi, A Shukla, S Nampoothiri, VH Sankar, ... Gene 567 (2), 173-181, 2015	27	2015
Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients KM Girisha, AM Bidchol, L Graul-Neumann, A Gupta, U Hehr, D Lessel, ... BMC Medical Genetics 17, 1-14, 2016	20	2016
A novel mutation (g. 106737G> T) in zone of polarizing activity regulatory sequence (ZRS) causes variable limb phenotypes in Werner mesomelia KM Girisha, AM Bidchol, PS Kamath, KH Shah, GR Mortier, S Mundlos, ... American Journal of Medical Genetics Part A 164 (4), 898-906, 2014	19	2014
White matter changes in GM1 gangliosidosis M Tuteja, AM Bidchol, KM Girisha, S Phadke Indian Pediatr 52 (2), 155-156, 2015	15	2015
A Novel Frameshift Mutation in TWIST2 Gene Causing Setleis Syndrome KM Girisha, AM Bidchol, MK Sarpangala, K Satyamoorthy The Indian Journal of Pediatrics 81, 302-304, 2014	14	2014
Exome sequencing identifies a dominant TNNT3 mutation in a large family with distal arthrogryposis SB Daly, H Shah, J O'sullivan, B Anderson, S Bhaskar, S Williams, ... Molecular Syndromology 5 (5), 218-228, 2014	13	2014
Novel mutation in an Indian patient with Methylmalonic Acidemia, cblA type KM Girisha, A Shrikiran, AM Bidchol, O Sakamoto, PM Gopinath, ... Indian journal of human genetics 18 (3), 346, 2012	7	2012
Marfan Syndrome with Systemic Lupus erythematosus A Alshdefat, AM Bidchol, A Alshdaifat, RA Baker TMR Integrative Nursing 4 (5), 172-175, 2020		2020

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