A citation-based method for searching scientific literature

Yosr Hamdi, Najah Mighri, Maroua Boujemaa, Nesrine Mejri, Sonia Ben Nasr, Mariem Ben Rekaya, Olfa Messaoud, Hanen Bouaziz, Yosra Berrazega, Haifa Rachdi, Olfa Jaidane, Nouha Daoud, Aref Zribi, Jihene Ayari, Houda El Benna, Soumaya Labidi, Jamel Ben Hassouna, Abderazzek Haddaoui, Khaled Rahal, Farouk Benna, Ridha Mrad, Slim Ben Ahmed, Hamouda Boussen, Samir Boubaker, Sonia Abdelhak. Front Oncol 2021
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Comorbidity in the Tunisian population.
L Romdhane, O Messaoud, Y Bouyacoub, E Kerkeni, C Naouali, L Cherif Ben Abdallah, A Tiar, C Charfeddine, K Monastiri, I Chabchoub,[...]. Clin Genet 2016
11
100

Consanguinity and Inbreeding in Health and Disease in North African Populations.
Lilia Romdhane, Nessrine Mezzi, Yosr Hamdi, Ghada El-Kamah, Abdelhamid Barakat, Sonia Abdelhak. Annu Rev Genomics Hum Genet 2019
22
100

[Atopic dermatitis in Tunisia: epidemiological and clinical aspects].
M Kharfi, H Bel Hadjali, A Khaled, I Mokhtar, M R Kamoun. Ann Dermatol Venereol 2001
5
100

Clinical and neuropsychological outcomes for children with phenylketonuria in Upper Egypt; a single-center study over 5 years.
Abdelrahim A Sadek, Mohammed H Hassan, Nesreen A Mohammed. Neuropsychiatr Dis Treat 2018
5
100

Specific aspects of consanguinity: some examples from the Tunisian population.
Lilia Romdhane, Nizar Ben Halim, Insaf Rejeb, Rym Kefi, Yosra Bouyacoub, Mariem Ben Rekaya, Habib Messai, Olfa Messaoud, Zied Riahi, Crystel Bonnet,[...]. Hum Hered 2014
14
100

Incidence of newborn screening disorders among 56632 infants in Central Saudi Arabia. A 6-year study.
Sarar Mohamed, Wafa Elsheikh, Aida I Al-Aqeel, Amal M Alhashem, Ali Alodaib, Lujane Alahaideb, Maher Almashary, Fahad Alharbi, Horia AlMalawi, Amer Ammari,[...]. Saudi Med J 2020
3
100

Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene.
Latifa Chkioua, Souhir Khedhiri, Oussama Grissa, Chaker Aloui, Hadhami Ben Turkia, Salima Ferchichi, Abdelhedi Miled, Roseline Froissart, Cecile Acquaviva, Sandrine Laradi. Meta Gene 2015
4
100


A lower-cost protocol for sickle cell disease neonatal screening in Tunisia.
Siala Hajer, Taboubi Neila, Hadj Fradj Sondess, Ouenniche Fekria, Aoun Nabila, Khedhri Mahbouba, Douiri Melika, Ouali Faida, Bibi Amina, Belhadj Raja,[...]. Ann Saudi Med 2012
7
100

Consanguinity: implications for practice, research, and policy.
Ahmad S Teebi, Hatem I El-Shanti. Lancet 2006
24
100

c.3623G > A mutation encodes a CFTR protein with impaired channel function.
Xiaoying Zhang, Jaspal S Hothi, Yanhui H Zhang, Saumini Srinivasan, Dennis C Stokes, Weiqiang Zhang. Respir Res 2016
8
100

Rapid Identification of Biallelic SPTB Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure.
Christopher M Richmond, Sally Campbell, Hee W Foo, Sebastian Lunke, Zornitza Stark, Amanda Moody, Elizabeth Bannister, Anthea Greenway, Natasha Brown. Mol Syndromol 2020
2
100

Inequities in newborn screening: Race and the role of medicaid.
Heeju Sohn, Stefan Timmermans. SSM Popul Health 2019
3
100

Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V.
M Kharrat, S Trabelsi, M Chaabouni, F Maazoul, L Kraoua, L Ben Jemaa, N Gandoura, S Barsaoui, Y Morel, R M'rad,[...]. Clin Genet 2010
18
100

Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes.
Enza Maria Valente, Clare V Logan, Soumaya Mougou-Zerelli, Jeong Ho Lee, Jennifer L Silhavy, Francesco Brancati, Miriam Iannicelli, Lorena Travaglini, Sveva Romani, Barbara Illi,[...]. Nat Genet 2010
184
100

Consanguinity and reproductive health among Arabs.
Ghazi O Tadmouri, Pratibha Nair, Tasneem Obeid, Mahmoud T Al Ali, Najib Al Khaja, Hanan A Hamamy. Reprod Health 2009
248
100


Dental-craniofacial manifestation and treatment of rare diseases.
En Luo, Hanghang Liu, Qiucheng Zhao, Bing Shi, Qianming Chen. Int J Oral Sci 2019
8
100

Personalized medicine in cystic fibrosis: genistein supplementation as a treatment option for patients with a rare S1045Y-CFTR mutation.
Kavisha Arora, Sunitha Yarlagadda, Weiqiang Zhang, ChangSuk Moon, Erin Bouquet, Saumini Srinivasan, Chunying Li, Dennis C Stokes, Anjaparavanda P Naren. Am J Physiol Lung Cell Mol Physiol 2016
7
100

Molecular characterization of X-linked adrenoleukodystrophy in a Tunisian family: identification of a novel missense mutation in the ABCD1 gene.
Fakhri Kallabi, Ikhlass Hadj Salem, Ghada Ben Salah, Hadhami Ben Turkia, Amel Ben Chehida, Neji Tebib, Faiza Fakhfakh, Hassen Kamoun. Neurodegener Dis 2013
4
100

The burden of rare diseases.
Carlos R Ferreira. Am J Med Genet A 2019
57
100

Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings.
Cynthia F Hinton, Cara T Mai, Sarah K Nabukera, Lorenzo D Botto, Lisa Feuchtbaum, Paul A Romitti, Ying Wang, Kimberly Noble Piper, Richard S Olney. Genet Med 2014
16
100

Burkitt lymphoma in a child with Bloom syndrome.
F Fedhila-Ben Ayed, W Douira-Khomsi, S Rhayem, M Jelassi, H Zribi, M Chaabouni, M Khemiri, I Bellagha, S Barsaoui. Arch Pediatr 2016
5
100

Identification of a CDH12 potential candidate genetic variant for an autosomal dominant form of transgrediens and progrediens palmoplantar keratoderma in a Tunisian family.
Cherine Charfeddine, Hamza Dallali, Ghaith Abdessalem, Kais Ghedira, Yosr Hamdi, Sahar Elouej, Zied Landoulsi, Valérie Delague, Arnaud Lagarde, Nicolas Levy,[...]. J Hum Genet 2020
3
100

[Molecular diagnosis of Gaucher disease in Tunisia].
W Cherif, H Ben Turkia, F Ben Rhouma, I Riahi, J Chemli, O Amaral, M C Sá Miranda, C Caillaud, N Kaabachi, N Tebib,[...]. Pathol Biol (Paris) 2013
1
100

[Molecular epidemiology of cystic fibrosis in Tunisia].
T Messaoud, S Bel Haj Fredj, A Bibi, J Elion, C Férec, S Fattoum. Ann Biol Clin (Paris) 2005
27
100

Global burden of genetic disease and the role of genetic screening.
I C Verma, R D Puri. Semin Fetal Neonatal Med 2015
25
100

Phenotypic expression of familial hypercholesterolaemia in central and southern Tunisia.
M N Slimane, H Pousse, F Maatoug, M Hammami, M H Ben Farhat. Atherosclerosis 1993
43
100

Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.
E M McNally, M R Passos-Bueno, C G Bönnemann, M Vainzof, E de Sá Moreira, H G Lidov, K B Othmane, P H Denton, J M Vance, M Zatz,[...]. Am J Hum Genet 1996
99
100

Preliminary study of haplotypes linked to the rare cystic fibrosis E1104X mutation.
S Oueslati, S Hadj Fredj, R Belhaj, H Siala, A Bibi, Taieb Messaoud. Acta Physiol Hung 2015
3
100

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.
O Messaoud, M Ben Rekaya, H Ouragini, S Benfadhel, H Azaiez, R Kefi, N Gouider-Khouja, I Mokhtar, A Amouri, M S Boubaker,[...]. Arch Dermatol Res 2012
18
100

Phylogeny and genetic structure of Tunisians and their position within Mediterranean populations.
Rym Kefi, Sana Hsouna, Nizar Ben Halim, Khaled Lasram, Lilia Romdhane, Habib Messai, Sonia Abdelhak. Mitochondrial DNA 2015
19
100

Identification and characterization of a novel MLH1 genomic rearrangement as the cause of HNPCC in a Tunisian family: evidence for a homologous Alu-mediated recombination.
Sana Aissi-Ben Moussa, Amel Moussa, Tonio Lovecchio, Nadia Kourda, Taoufik Najjar, Sarra Ben Jilani, Amel El Gaaied, Nicole Porchet, Mohamed Manai, Marie-Pierre Buisine. Fam Cancer 2009
19
100

First report of molecular diagnosis of Tunisian hemophiliacs A: identification of 8 novel causative mutations.
Hejer Elmahmoudi, Houssein Khodjet-el-khil, Edvard Wigren, Asma Jlizi, Kaouther Zahra, Dorothé Pellechia, Christine Vinciguerra, Balkis Meddeb, Amel Ben Ammar Elggaaied, Emna Gouider. Diagn Pathol 2012
8
100

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care.
Marie De Antonio, Céline Dogan, Ferroudja Daidj, Bruno Eymard, Jack Puymirat, Jean Mathieu, Cynthia Gagnon, Sandrine Katsahian, Dalil Hamroun, Guillaume Bassez. Orphanet J Rare Dis 2019
2
100

Molecular characterization of MPS IIIA, MPS IIIB and MPS IIIC in Tunisian patients.
S Ouesleti, V Brunel, H Ben Turkia, H Dranguet, A Miled, N Miladi, M F Ben Dridi, A Lavoinne, P Saugier-Veber, S Bekri. Clin Chim Acta 2011
12
100

[Neonatal hearing screening with transient otoacoustic emissions: pilot study].
Emira Ben Hamida Nouaili, Sihem Chaouachi, Ahlem Bezzine, Majda Hamadi, Chiraz Mbarek, Lotfi Benlallehom, Zahra Marrakchi. Tunis Med 2010
1
100

A novel CASR mutation in a Tunisian FHH/NSHPT family associated with a mental retardation.
Sana Sfar, Ahlem Afaya Bzéouich, Emna Kerkeni, Sofiane Bouaziz, Mohamed Fadhel Najjar, Lotfi Chouchane, Kamel Monastiri. Mol Biol Rep 2012
5
100


An Arab registry for type 1 diabetes: global benefits for type 1 diabetes patients.
Hatem Zayed, Allal Ouhtit, Rajaa El Bekay. Curr Med Res Opin 2016
6
100


Rare diseases under different levels of economic analysis: current activities, challenges and perspectives.
Sara Cannizzo, Valentina Lorenzoni, Ilaria Palla, Salvatore Pirri, Leopoldo Trieste, Isotta Triulzi, Giuseppe Turchetti. RMD Open 2018
14
100

Systemic lupus erythematosus, antiphospholipid syndrome and Hashimoto thyroiditis occurring in a patient with Niemann-Pick disease: a second case.
Wafa Baya, Fatma Ben Fredj, Imen Ben Hassine, Jihed Anoun, Anis Mzabi, Monia Karmani, Amel Rezgui, Mohamed Adnane Laatiri, Chedia Laouani Kechrid. Pan Afr Med J 2020
1
100

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
Zied Riahi, Hassen Hammami, Houyem Ouragini, Habib Messai, Rim Zainine, Yosra Bouyacoub, Lilia Romdhane, Donia Essaid, Rym Kefi, Mohsen Rhimi,[...]. Gene 2013
26
100

Molecular characterization of maple syrup urine disease patients from Tunisia.
N Jaafar, A Moleirinho, E Kerkeni, K Monastiri, H Seboui, A Amorim, M J Prata, S Quental. Gene 2013
8
100

Health system challenges of NCDs in Tunisia.
Habiba Ben Romdhane, Faten Tlili, Afef Skhiri, Shahaduz Zaman, Peter Phillimore. Int J Public Health 2015
13
100

VIII World Rett Syndrome Congress & Symposium of rare diseases, Kazan, Russia.
Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov, Thomas Bertrand. Mol Cytogenet 2018
1
100

[Neonatal screening of G6PD deficiency in Tunisia].
N Guellouz, I Ben Mansour, M Ouederni, S Jabnoun, S Kacem, Ch Mokrani, R Kastally, M K Chahed, N Khrouf. Arch Inst Pasteur Tunis 2010
8
100

Obesity and association with area of residence, gender and socio-economic factors in Algerian and Tunisian adults.
Madjid Atek, Pierre Traissac, Jalila El Ati, Youcef Laid, Hajer Aounallah-Skhiri, Sabrina Eymard-Duvernay, Nadia Mézimèche, Souha Bougatef, Chiraz Béji, Leila Boutekdjiret,[...]. PLoS One 2013
25
100



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.