Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 137 Records) |
Query Trace: ASL[original query] |
---|
The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey. Balkan medical journal 2021 Nov 38 (6): 357-364. Erdo?an Murat, Köse Mehmet, Pekcan Sevgi, Hangül Melih, Balta Burhan, Kiraz Asl?han, Ak?nc? Gönen Gizem, Zamani Ay?e Gül, Y?ld?r?m Mahmut Selam, Ramasl? Gürsoy Tu?ba, Ezgu Fatih, ?i?manlar Eyüpo?lu Tu?ba, Tana Aslan Ay |
Determination of High-Resolution HLA-DQB1 Suballeles and IL-17 Polymorphisms in Turkish Pediatric Patients. Journal of pediatric genetics 2022 8 11 (3): 192-197. Eldem Asl?, Ayna Tülay K?l?çaslan, Baran Ma?allah, Soyöz Mustafa, Pirim ?brah |
Comparison of S gene mutations in patients with occult and chronic hepatitis B virus infection. Virus research 2022 7 318 198855. Cakal Bulent, Cavus Bilger, Atasoy Alp, Altunok Damla, Poda Mehves, Bulakc? Mesut, Gulluoglu Mine, Demirci Mehmet, Sener Leyla Turker, Arslan Asl? Berru, Arikan Muzaffer, Akyuz Fil |
Association of BDNF Gene Val66Met Polymorphism with Suicide Attempts, Focused Attention and Response Inhibition in Patients with Schizophrenia. Noro psikiyatri arsivi 2022 59 (2): 91-97. Bolat Kaya Özlem, Kaya Hasan, Civan Kahve Aybeniz, Enez Darçin Asl?, Yalçin Çavu? Raziye Serçin, Dilbaz Nesr |
Precore/core mutations of hepatitis B virus genotype D arising in different states of infection. Clinical and experimental hepatology 2022 4 8 (1): 21-28. Sanaei Neda, Hashemi Seyed Mohammad Ali, Dehno Seyedeh Zahra Salehi, Asl Mozhde Mahmoudi, Moini Maryam, Malek-Hosseini Seyed Ali, Hosseini Seyed Younes, Sarvari Jam |
Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY. Leukemia 2022 12 37 (2): 339-347. Mansouri Larry, Thorvaldsdottir Birna, Sutton Lesley-Ann, Karakatsoulis Georgios, Meggendorfer Manja, Parker Helen, Nadeu Ferran, Brieghel Christian, Laidou Stamatia, Moia Riccardo, Rossi Davide, Catherwood Mark, Kotaskova Jana, Delgado Julio, Rodríguez-Vicente Ana E, Benito Rocío, Rigolin Gian Matteo, Bonfiglio Silvia, Scarfo Lydia, Mattsson Mattias, Davis Zadie, Gogia Ajay, Rani Lata, Baliakas Panagiotis, Foroughi-Asl Hassan, Jylhä Cecilia, Skaftason Aron, Rapado Inmaculada, Miras Fatima, Martinez-Lopez Joaquín, de la Serna Javier, Rivas Jesús María Hernández, Thornton Patrick, Larráyoz María José, Calasanz María José, Fésüs Viktória, Mátrai Zoltán, Bödör Csaba, Smedby Karin E, Espinet Blanca, Puiggros Anna, Gupta Ritu, Bullinger Lars, Bosch Francesc, Tazón-Vega Bárbara, Baran-Marszak Fanny, Oscier David, Nguyen-Khac Florence, Zenz Thorsten, Terol Maria Jose, Cuneo Antonio, Hernández-Sánchez María, Pospisilova Sarka, Mills Ken, Gaidano Gianluca, Niemann Carsten U, Campo Elias, Strefford Jonathan C, Ghia Paolo, Stamatopoulos Kostas, Rosenquist Richa |
Analysis of H-ras Mutations and Immunohistochemistry in Recurrence Cases of High-Grade Oral Squamous Cell Carcinoma. Head and neck pathology 2022 11 . Hamidavi Asl Azin, Shirkhoda Mohammad, Saffar Hana, Allameh Abdolam |
Evaluation of serum vascular endothelial growth factor level and findings of nailfold capillaroscopy by dermatoscope in the differential diagnosis of palmoplantar psoriasis and palmoplantar eczema. Microvascular research 2022 10 145 104441. Avc? Elif Bal, Erdemir Vefa Asl?, Erdem Ozan, I??k Reyhan, Aksu Ay?e Esra Ko |
COMT Val158Met Polymorphism Influences the Cerebral Blood Flow Changes Related to Psychomotor Retardation in Major Depressive Disorder. Neuropsychiatric disease and treatment 2022 10 18 2159-2169. Yin Yingying, Xie Chunming, Zhang Haisan, Zhang Hongxing, Zhang Zhijun, Yuan Yongg |
The impact of leptin and its receptor polymorphisms on type 1 diabetes in a population of northwest Iran. Annals of human biology 2022 10 1-6. Azimnasab-Sorkhabi Parviz, Soltani-Asl Maryam, Kfoury José Roberto, Algenstaedt Petra, Mehmetzade Hakan Farzin, Hashemi Aghdam Yash |
PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran. Iranian journal of basic medical sciences 2022 1 24 (9): 1190-1195. Jafarzadeh Esfehani Reza, Eslahi Atieh, Beiraghi Toosi Mehran, Sadr-Nabavi Ariane, Kerachian Mohammad Amin, Asl Mohajeri Mahsa Sadat, Farjami Mahsa, Alizade Farzaneh, Mojarrad Maj |
Dementia risk and dynamic response to exercise: A non-randomized clinical trial. PloS one 2022 17 (7): e0265860. Vidoni Eric D, Morris Jill K, Palmer Jacqueline A, Li Yanming, White Dreu, Kueck Paul J, John Casey S, Honea Robyn A, Lepping Rebecca J, Lee Phil, Mahnken Jonathan D, Martin Laura E, Billinger Sandra |
Whole Exome Sequencing to Find Candidate Variants for the Prediction of Kidney Transplantation Efficacy. Genes 2023 6 14 (6): . Seyed Mohammad Kazem Aghamir, Hassan Roudgari, Hassan Heidari, Mohammad Salimi Asl, Yousef Jafari Abarghan, Venous Soleimani, Rahil Mashhadi, Fatemeh Khata |
Cortical high-flow sign on arterial spin labeling: a novel biomarker for IDH-mutation and 1p/19q-codeletion status in diffuse gliomas without intense contrast enhancement. Neuroradiology 2023 6 . Koji Yamashita, Osamu Togao, Kazufumi Kikuchi, Daisuke Kuga, Yuhei Sangatsuda, Yutaka Fujioka, Izumi Kinoshita, Makoto Obara, Koji Yoshimoto, Kousei Ishiga |
PROKR2 Mutations in Patients with Short Stature Who Have Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiency. Journal of clinical research in pediatric endocrinology 2023 6 . Asl? Derya Kardelen, Adam Najafli, Firdevs Ba?, Birsen Karaman, Güven Toksoy, ?ükran Poyrazo?lu, ?ahin Avc?, Umut Altuno?lu, Zehra Yava? Abal?, Ay?e P?nar Öztürk, Esin Karak?l?ç Özturan, Seher Ba?aran, Feyza Darendeliler, Z Oya Uygun |
Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. Turkish archives of pediatrics 2023 6 . Nilay Güne?, Dilek Uluda? Alkaya, Asl? Toylu, Püren Özüdo?ru, Evrim Çifçi Sunamak, Ali ?eker, Bilal Demir, Sebuh Kuru?o?lu, Ercan M?hç?, Beyhan Tüys |
Association between mannose binding lectin gene polymorphisms and clinical severity of COVID-19 in children. Molecular biology reports 2023 5 1-7. Dilek Yilmaz, Mustafa Soyoz, Asl?han Sahin, Burcu Cerci-Alkac, Hatice Ilayhan Karahan-Coven, Y?ld?z Ekemen-Keles, Gulnihan Ustundag, Ahu Kara-Aksay, Nisel Yilmaz, ?brahim Pir |
Evaluation of a warfarin dosing algorithm including CYP2C9, VKORC1, and CYP4F2 polymorphisms and non-genetic determinants for the Iranian population. Pharmacological reports : PR 2023 4 . Farajzadeh-Dehkordi Mahvash, Samiee-Rad Fatemeh, Farzam Seyed Saeed, Javadi Amir, Cheraghi Sara, Hamedi-Asl Dariush, Rahmani Bab |
The effect of ACE2 receptor, IFN-?, and TNF-? polymorphisms on the severity and prognosis of the disease in SARS-CoV-2 infection. Journal of investigative medicine : the official publication of the American Federation for Clinical Research 2023 3 10815589231158379. Esen Say?n Gülensoy, Basak Celtikci, Leyla Özer, Asl?han Alhan, Evrim Eylem Akp?n |
Disease and Quality of Life Aspects of Cat Allergy in Non-Pet Owners with Allergic Rhinitis. International archives of allergy and immunology 2023 3 1-9. Yüksel Asl?er Nesibe Gül, Saatçi Özlem, Aslier Musta |
KRAS, NRAS, BRAF, and PIK3CA mutation rates, clinicopathological association, and their prognostic value in Iranian colorectal cancer patients. Journal of clinical laboratory analysis 2023 3 e24868. Mirzapoor Abbasabadi Zohreh, Hamedi Asl Dariush, Rahmani Babak, Shahbadori Rozhin, Karami Sara, Peymani Amir, Taghizadeh Sara, Samiee Rad Fatem |
Are MUC5B and TERT mutations genetic risk factors for pulmonary fibrosis in individuals with severe COVID-19? Tuberkuloz ve toraks 2023 3 71 (1): 34-40. Yetkin Nur Aleyna, Kiraz Asl?han, Baran Ketencio?lu Burcu, Bol Canan, Tutar Nu |
Cutaneous vascular structure and perfusion in patients with chronic plaque psoriasis. Clinical and experimental dermatology 2023 2 48 (3): 181-187. Luengas-Martinez Andrea, Kamaly-Asl Anna, Chaudhry Iskander H, Brenchley Paul E C, Young Helen |
Can TERT rs2853669 polymorphysm indicate fibrosis in sarcoidosis? Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG 2023 12 40 (4): e2023043. Sümeyye Kement, Eda Turgut Ugurtay, Asl? Tanr?vermis Say?t, P?nar Tasc?, Meftun Uns |
Complement gene mutations in children with C3 glomerulopathy: do they affect the response to mycophenolate mofetil? Pediatric nephrology (Berlin, Germany) 2023 12 . Neslihan Günay, ?smail Dursun, ?brahim Gökçe, Mehtap Akbal?k Kara, Demet Tekcan, Neslihan Çiçek, Meral Torun Bayram, Mustafa Koyun, Nida Dinçel, Hasan Dursun, Seha Sayg?l?, Zeynep Nagehan Yürük Y?ld?r?m, Selçuk Yüksel, Osman Dönmez, Sibel Yel, Beltinge Demircio?lu K?l?ç, Özlem Aydo?, Bahriye Atm??, Aysun Çalt?k Y?lmaz, Sevcan A Bakkalo?lu, Mehmet Baha Aytaç, Mehmet Ta?demir, Belde Kasap Demir, Alper Soylu, Elif Çomak, Asl? Kantar Öz?ahin, Alper Kaçar, Nur Canpolat, Alev Y?lmaz, ?lknur Giri?gen, Kadirye Betül Akkoyunlu, Harika Alpay, Hakan M Poyrazo? |
Genetic, Surgical and Oncological Approach to Breast Cancer, with BRCA1, BRCA2, CDH1, PALB2, PTEN and TP53 Variants. European journal of breast health 2023 1 19 (1): 55-69. Suba??o?lu Asl?, Güç Zeynep Gülsüm, Gür Emine Özlem, Tekindal Mustafa Agah, Atahan Murat Kem |
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID-19 and disease severity in patients at high risk for hereditary thrombophilia. Journal of medical virology 2023 1 95 (2): e28457. Kiraz Asl?han, Sezer Ozlem, Alemdar Adem, Canbek Sezin, Duman Nilgun, Bisgin At?l, Cora Tulin, Ruhi Hatice Ilg?n, Ergoren Mahmut Cerkez, Geçkinli Bilgen Bilge, Sag Sebnem Ozemri, Gözden Hilmi Erdem, Oz Ozlem, Alt?nta? Zuhal Mert, Yalc?ntepe Sinem, Keskin Adem, Tak Ay?egül Yabac?, Paskal ?eyma Akta?, Yürekli U?ur Fahri, Demirtas Mercan, Evren Emine Unal, Hanta Abdullah, Ba?demirci Mü?erref, Suer Kaya, Balta Burhan, Kocak Nadir, Karabulut Halil Gürhan, Cobanogullar? Havva, Ate? Esra Arslan, Bozdo?an Sevcan Tu?, Eker Damla, Ekinci Sadiye, Nergiz Süleyman, Tuncal? Timur, Yagbasan Serap, Alavanda Ceren, Kutlay Nuket Yurur, Evren Hakan, Erdo?an Murat, Alt?ner Sule, Sanlidag Tamer, Gonen Gizem Ak?nc?, Vicdan Arzu, Eras Nazan, Eker Hatice Koçak, Balasar Ozgür, Tuncel Gulten, Dundar Munis, Gurkan Hakan, Temel Sehime Guls |
BTK and PLCG2 remain unmutated in one third of patients with CLL relapsing on ibrutinib. Blood advances 2023 1 . Bonfiglio Silvia, Sutton Lesley-Ann, Ljungström Viktor, Capasso Antonella, Pandzic Tatjana, Weström Simone, Foroughi-Asl Hassan, Skaftason Aron, Gellerbring Anna, Lyander Anna, Gandini Francesca, Gaidano Gianluca, Trentin Livio, Bonello Lisa, Reda Gianluigi, Bödör Csaba, Stavroyianni Niki, Tam Constantine S, Marasca Roberto, Forconi Francesco, Panayiotidis Panayiotis, Ringshausen Ingo, Jaksic Ozren, Frustaci Anna Maria, Iyengar Sunil, Coscia Marta, Mulligan Stephen P, Ysebaert Loïc, Strugov Vladimir, Pavlovsky Carolina, Walewska Renata, Österborg Anders, Cortese Diego, Ranghetti Pamela, Baliakas Panagiotis, Stamatopoulos Kostas, Scarfò Lydia, Rosenquist Richard, Ghia Pao |
Correction: Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY. Leukemia 2023 1 37 (2): 504. Mansouri Larry, Thorvaldsdottir Birna, Sutton Lesley-Ann, Karakatsoulis Georgios, Meggendorfer Manja, Parker Helen, Nadeu Ferran, Brieghel Christian, Laidou Stamatia, Moia Riccardo, Rossi Davide, Catherwood Mark, Kotaskova Jana, Delgado Julio, Rodríguez-Vicente Ana E, Benito Rocío, Rigolin Gian Matteo, Bonfiglio Silvia, Scarfo Lydia, Mattsson Mattias, Davis Zadie, Gogia Ajay, Rani Lata, Baliakas Panagiotis, Foroughi-Asl Hassan, Jylhä Cecilia, Skaftason Aron, Rapado Inmaculada, Miras Fatima, Martinez-Lopez Joaquín, de la Serna Javier, Rivas Jesús María Hernández, Thornton Patrick, Larráyoz María José, Calasanz María José, Fésüs Viktória, Mátrai Zoltán, Bödör Csaba, Smedby Karin E, Espinet Blanca, Puiggros Anna, Gupta Ritu, Bullinger Lars, Bosch Francesc, Tazón-Vega Bárbara, Baran-Marszak Fanny, Oscier David, Nguyen-Khac Florence, Zenz Thorsten, Terol Maria Jose, Cuneo Antonio, Hernández-Sánchez María, Pospisilova Sarka, Mills Ken, Gaidano Gianluca, Niemann Carsten U, Campo Elias, Strefford Jonathan C, Ghia Paolo, Stamatopoulos Kostas, Rosenquist Richa |
A Novel Deleterious MYO15A Gene Mutation Causes Nonsyndromic Hearing Loss. Iranian journal of otorhinolaryngology 2024 1 36 (1): 355-360. Mostafa Neissi, Adnan Issa Al-Badran, Javad Mohammadi-A |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: