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ArticlesPeer ReviewedFull Text
Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities
Author / Creator:Najafi, Kimia ; Mehrjoo, Zohreh ; Ardalani, Fariba ; Ghaderi-Sohi, Siavash ; Kariminejad, Ariana ; Kariminejad, Roxana ; Najmabadi, Hossein
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2021-03, Vol.11 (1), p.6952-6952, Article 6952
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ArticlesPeer ReviewedFull Text
Different antithrombotic strategies to prevent cardiovascular complications in Kawasaki patients: a systematic review and meta-analysis
Author / Creator:Assempoor, Ramin ; Abroy, Alireza Sattari ; Azarboo, Alireza ; Ghaseminejad-Raeini, Amirhossein ; Najafi, Kimia ; Hosseini, Kaveh
Publisher:England: BioMed Central Ltd
Journal title:BMC pediatrics, 2024-11, Vol.24 (1), p.738-14, Article 738
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ArticlesPeer ReviewedFull Text
Association between sleep duration and hypertension incidence: Systematic review and meta-analysis of cohort studies
Author / Creator:Hosseini, Kaveh ; Soleimani, Hamidreza ; Tavakoli, Kiarash ; Maghsoudi, Milad ; Heydari, Narges ; Farahvash, Yasmin ; Etemadi, Ali ; Najafi, Kimia ; Askari, Mani K. ; Gupta, Rahul ; Hakim, Diaa ; Rahimi, Kazem
Publisher:United States: Public Library of Science
Journal title:PloS one, 2024-07, Vol.19 (7), p.e0307120
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ArticlesPeer ReviewedFull Text
The association between metabolic syndrome and major adverse cardiac and cerebrovascular events in patients with acute coronary syndrome undergoing percutaneous coronary intervention
Author / Creator:Hosseini, Kaveh ; Khalaji, Amirmohammad ; Behnoush, Amir Hossein ; Soleimani, Hamidreza ; Mehrban, Saghar ; Amirsardari, Zahra ; Najafi, Kimia ; Fathian Sabet, Mehrshad ; Hosseini Mohammadi, Negin Sadat ; Shojaei, Shayan ; Masoudkabir, Farzad ; Aghajani, Hassan ; Mehrani, Mehdi ; Razjouyan, Hadie ; Hernandez, Adrian V.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2024-01, Vol.14 (1), p.697-697, Article 697
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ArticlesPeer ReviewedFull Text
Triglyceride-glucose index as a predictor of cardiac adverse events in acute coronary syndrome patients undergoing percutaneous coronary intervention: role of diabetes
Author / Creator:Khalaji, Amirmohammad ; Behnoush, Amir Hossein ; Pasebani, Yeganeh ; Rafati, Ali ; Mahmoodi, Tara ; Arzhangzadeh, Alireza ; Shamshiri Khamene, Sima ; MohammadKhawajah, Izat ; Mehrani, Mehdi ; Vasheghani-Farahani, Ali ; Masoudkabir, Farzad ; Najafi, Kimia ; Askari, Mani K. ; Harrison, Anil ; Nelson, John R. ; Hosseini, Kaveh ; Hernandez, Adrian V.
Publisher:England: BioMed Central Ltd
Journal title:BMC cardiovascular disorders, 2024-09, Vol.24 (1), p.514-10, Article 514
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ArticlesPeer ReviewedFull Text
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome
Author / Creator:Kuechler, Alma ; Zink, Alexander M ; Wieland, Thomas ; Lüdecke, Hermann-Josef ; Cremer, Kirsten ; Salviati, Leonardo ; Magini, Pamela ; Najafi, Kimia ; Zweier, Christiane ; Czeschik, Johanna Christina ; Aretz, Stefan ; Endele, Sabine ; Tamburrino, Federica ; Pinato, Claudia ; Clementi, Maurizio ; Gundlach, Jasmin ; Maylahn, Carina ; Mazzanti, Laura ; Wohlleber, Eva ; Schwarzmayr, Thomas ; Kariminejad, Roxana ; Schlessinger, Avner ; Wieczorek, Dagmar ; Strom, Tim M ; Novarino, Gaia ; Engels, Hartmut
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2015-06, Vol.23 (6), p.753-760
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ArticlesPeer ReviewedFull Text
Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails
Author / Creator:Kariminejad, Ariana ; Ajeawung, Norbert Fonya ; Bozorgmehr, Bita ; Dionne-Laporte, Alexandre ; Molidperee, Sirinart ; Najafi, Kimia ; Gibbs, Richard A ; Lee, Brendan H ; Hennekam, Raoul C ; Campeau, Philippe M
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2017-04, Vol.62 (4), p.465-471
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ArticlesPeer ReviewedFull Text
Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient
Author / Creator:Taghdiri, Maryam ; Kashef, Atie ; Abbassi, Golemaryam ; Moshtagh, Azadeh ; Sadatian, Neda ; Fardaei, Majid ; Najafi, Kimia ; Kariminejad, Roxana
Publisher:England: John Wiley & Sons, Inc
Journal title:Clinical case reports, 2019-06, Vol.7 (6), p.1149-1153
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ArticlesPeer ReviewedFull Text
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases
Author / Creator:Najafi, Kimia ; Gholami, Soheila ; Moshtagh, Azadeh ; Bazrgar, Masood ; Sadatian, Neda ; Abbasi, Golemaryam ; Rostami, Parvin ; Khalili, Soheila ; Babanejad, Mojgan ; Nourmohammadi, Bahareh ; Faramarzi Garous, Negin ; Najmabadi, Hossein ; Kariminejad, Roxana
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2019-08, Vol.7 (8), p.e820-n/a
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ArticlesPeer ReviewedFull Text
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis
Author / Creator:Kariminejad, Mohamad Hassan ; Kariminejad, Ariana ; Sadatian, Neda ; Abbassi, Gole Maryam ; Moshtagh, Azadeh ; Hosseini, Kaveh ; Kariminejad, Roxana ; Najafi, Kimia ; Bazrgar, Masood
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Case reports in genetics, 2017-01, Vol.2017 (2017), p.1-4
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ArticlesPeer ReviewedFull Text
Efficacy of Acellular Dermal Matrix Versus Free Gingival Graft for Increasing the Width of Attached Gingiva: A Clinical Trial
Author / Creator:Naddafpour, Nima ; Mozaffari, Asieh ; Ghaedi, Baharak ; Najafi, Kimia ; Ghaffari, Arash
Publisher:Diyarbakir: Ectodermal Dysplasia Group - Turkey
Journal title:Journal of International Dental & Medical Research, 2019-01, Vol.12 (4), p.1426-1432
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ArticlesFull Text
Knowledge, Attitudes and Practice of Hepatitis B vaccination among Iranian dentists
Author / Creator:Hamissi, Jalaleddin ; Tabari, Zahra Alizadeh ; Najafi, Kimia ; Hamissi, Hesameddin ; Hamissi, Zahra
Publisher:Sarajevo: DRUNPP Association
Journal title:International journal of collaborative research on internal medicine & public health, 2014-07, Vol.6 (7), p.199
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ReportsFull Text
Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient
Author / Creator:Taghdiri, Maryam ; Kashef, Atie ; Abbassi, Golemaryam ; Moshtagh, Azadeh ; Sadatian, Neda ; Fardaei, Majid ; Najafi, Kimia ; Kariminejad, Roxana
Journal title:Clinical case reports, 2019, Vol.7 (6), p.1149-1153
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ReportsFull Text
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis
Author / Creator:Najafi, Kimia ; Kariminejad, Roxana ; Hosseini, Kaveh ; Moshtagh, Azadeh ; Abbassi, Gole Maryam ; Sadatian, Neda ; Bazrgar, Masood ; Kariminejad, Ariana ; Kariminejad, Mohamad Hassan
Journal title:Case reports in genetics, 2017, Vol.2017, p.2706098-2706098
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Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

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Different antithrombotic strategies to prevent cardiovascular complications in Kawasaki patients: a systematic review and meta-analysis

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Association between sleep duration and hypertension incidence: Systematic review and meta-analysis of cohort studies

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The association between metabolic syndrome and major adverse cardiac and cerebrovascular events in patients with acute coronary syndrome undergoing percutaneous coronary intervention

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Triglyceride-glucose index as a predictor of cardiac adverse events in acute coronary syndrome patients undergoing percutaneous coronary intervention: role of diabetes

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Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

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Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

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Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

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Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis

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Efficacy of Acellular Dermal Matrix Versus Free Gingival Graft for Increasing the Width of Attached Gingiva: A Clinical Trial

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Knowledge, Attitudes and Practice of Hepatitis B vaccination among Iranian dentists

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

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Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis

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