| Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ... Nature genetics 36 (5), 449-451, 2004 | 1865 | 2004 |
| Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A S Züchner, IV Mersiyanova, M Muglia, N Bissar-Tadmouri, J Rochelle, ... Nature genetics 36 (5), 449-451, 2004 | 1859 | 2004 |
| Biomedical publications in an unstable region: the Arab world, 1988–2002 GO Tadmouri, N Bissar-Tadmouri The Lancet 362 (9397), 1766, 2003 | 97 | 2003 |
| Clinicopathological and genetic study of early-onset demyelinating neuropathy Y Parman, E Battaloğlu, I Barış, B Bilir, M Poyraz, N Bissar-Tadmouri, ... Brain 127 (11), 2540-2550, 2004 | 95 | 2004 |
| Bibliometric analyses of biomedical research outputs in Lebanon and the United Arab Emirates (1988–2007) N Bissar-Tadmouri, GO Tadmouri Saudi med J 30 (1), 130-139, 2009 | 72 | 2009 |
| Biomedical research in the Kingdom of Saudi Arabia (1982-2000) GO Tadmouri, NB Tadmouri Saudi Med J 23 (1), 20-24, 2002 | 72 | 2002 |
| Population relationships in the Mediterranean revealed by autosomal genetic data (Alu and Alu/STR compound systems MP González-Pérez E, Esteban E, Via M, Gayà-Vidal M, Athanasiadis G ... American Journal of Physical Anthropology 141, 430-439, 2010 | 50* | 2010 |
| Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients N Bissar‐Tadmouri, Y Parman, L Boutrand, F Deymeer, P Serdaroglu, ... Clinical genetics 58 (5), 396-402, 2000 | 46 | 2000 |
| Bibliographic indexes in biomedicine. Scientists GO Tadmouri, N Bissar-Tadmouri | 43 | 2004 |
| Bibliographic indexes in biomedicine. Scientists GO Tadmouri, N Bissar-Tadmouri | 43 | 2004 |
| X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblings KS Bissar-Tadmouri N,Donahue WL,Al-Gazali L,Nelson SF,Bayrak-Toydemir P American Journal of Medical Genetics A 164, 164-169, 2014 | 33 | 2014 |
| Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene N Bissar-Tadmouri, E Nelis, S Zuchner, Y Parman, F Deymeer, ... Neurology 62 (9), 1522-1525, 2004 | 22 | 2004 |
| Geography of biomedical publications GO Tadmouri, N Bissar-Tadmouri The Lancet 363 (9407), 489-490, 2004 | 19 | 2004 |
| Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus. M Celik, H Forta, Y Parman, N Bissar-Tadmouri, K Demirkirkan, ... Diabetic Medicine 18 (8), 2001 | 19 | 2001 |
| Genetic disorders in Arabs as for OMIM. GO Tadmouri, N Bissar-Tadmouri Saudi medical journal 20 (1), 4-18, 1999 | 13* | 1999 |
| An unexpected wide population variation of the G1733A polymorphism of the androgen receptor gene: data on the Mediterranean region. MP Esteban E, Via M, González-Pérez E, Santamaría J, Dugoujon JM, Vona G ... Am J Hum Biol 17 (6), 690-695, 2005 | 8 | 2005 |
| Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1 patients of Turkish origin: S54P,[I30del; GVYI29ins] N Bissar-Tadmouri, Y Gulsen-Parman, P Latour, F Deymeer, ... Human Mutation 14 (5), 449, 1999 | 6 | 1999 |
| Different evolutionary histories of the Coagulation Factor VII gene in human populations? G Athanasiadis, E Esteban, M Gayà‐Vidal, JM Dugoujon, N Moschonas, ... Annals of Human Genetics 74 (1), 34-45, 2010 | 5 | 2010 |
| Exome Sequencing Identifies a Novel Mutation in HEXB Associated with Juvenile Sandhoff Disease in a Consanguineous Family with Movement Disorders and Intellectual Disability S Kantarci, N Bissar-Tadmouri, MB Johnson, RS Hill, A Megarbane, ... JOURNAL OF MOLECULAR DIAGNOSTICS 15 (6), 851-851, 2013 | | 2013 |
| Genetic structure in human populations from the Western Mediterranean based on variation from five genomic regions. G Athanasiadis, M GAYÀ VIDAL, M Gibert, JM Dugoujon, N Moschonas, ... The EMBO Meeting 2010 abstract book, 2010 | | 2010 |
