2022

Abdelgawad R, Rathod YD, Alshammari M, Kelly L, Hübner CA, Aguilar-Bryan L, Di Fulvio M. Loss of Slc12a2 specifically in pancreatic β-cells drives metabolic syndrome in mice. PLoS One. 2022; 17: e0279560.
Alves G, Ornellas MH, Liehr T. The role of Calmodulin Binding Transcription Activator 1 (CAMTA1) gene and its putative genetic partners in the human nervous system. Psychogeriatrics 2022, 22 :869-878.
Akbari M, Taheri M, Mehrpoor G, Eslami S, Hussen BM, Ghafouri-Fard S, Arefian N. Assessment of ACE1 variants and ACE1/ACE2 expression in COVID-19 patients. Vasc Pharmacol. 2022; 142: 106934.
Akbari M, Eghtedarian R, Hussen BM, Eslami S, Taheri M, Neishabouri SM, Ghafouri-Fard S. Assessment of expression of regulatory T cell differentiation genes in autism spectrum disorder. Front Mol Neurosci. 2022; 15: 939224.
Akbari M, Badrlou E, Eslami S, Hussen BM, Taheri M, Neishabouri SM, Ghafouri-Fard S. Association between angiotensin I converting enzyme gene polymorphisms and risk of autism in Iranian population. Hum Gene. 2022; 33: 201046.
Akbari M, Eshghyar F, Gholipour M, Eslami S, Hussen BM, Taheri M, Omrani MD, Ghafouri-Fard S. Expression analysis of mTOR-associated lncRNAs in multiple sclerosis. Metab Brain Dis. 2022; 37: 2061-2066.
Akbari M, Akhavan-Bahabadi M, Shafigh N, Taheriazam A, Hussen BM, Sayad A, Fathi M, Taheri M, Ghafouri-Fard S, Fathi M. Expression analysis of IFNAR1 and TYK2 transcripts in COVID-19 patients. Cytokine. 2022; 153: 155849.
Asadi MR, Talebi M, Gharesouran J, Sabaie H, Jalaiei A, Arsang-Jang S, Taheri M, Sayad A, Rezazadeh M. Analysis of ROQUIN, Tristetraprolin (TTP), and BDNF/miR-16/TTP regulatory axis in late onset Alzheimer's disease. Front Aging Neurosci. 2022; 14: 933019.
Asadi MR, Moslehian MS, Sabaie H, Sharifi-Bonab M, Hakimi P, Hussen BM, Taheri M, Rakhshan A, Rezazadeh M. CircRNA-associated CeRNAs regulatory axes in retinoblastoma: a systematic scoping review. Front Oncol. 2022; 12: 910470.
Azawi S, Balachandran M, Kramer F, Kankel S, Rincic M, Liehr T. Molecular cytogenetic characterization of urethane induced murine lung cell line LA-4 as model for human squamous cell lung cancer. Mol Clin Oncol 2022, 16: 9.
Azawi S, Barf L-M, Liehr T, Kankel S, Rincic M. First cytogenomic characterization of murine testicular tumor cell line I-10. OBM Genetics 2022, 6: 159.
Azawi S, Kankel S, Liehr T, Rincic M. First cytogenomic characterization of murine testis tumor cell line MLTC-1. MEBM 2022, 4: 10-14.
Azawi S, Kramer F, Liehr T, Rincic M. First cytogenomic characterization of murine cutaneous sarcoma cell line TSC2ang1. Science Technology and Engineering Journal (STEJ) 2022, 8:1-16
Baba N, Lengyel A, Pinti E, Yapici E, Schreyer I, Liehr T, Fekete G, Eggermann T. Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes. Mol Cytogenet 2022, 15:19.
Bahrami Y, Bouk S, Kakaei E, Taheri M. Natural products from Actinobacteria as a potential source of new therapies against colorectal cancer: A review. Front Pharmacol. 2022; 13: 929161.
Barbaro V, Orvieto A, Alvisi G, Bertolin M, Bonelli F, Liehr T, Harutyunyan T, Kankel S, Joksic G, Ferrari S, Daniele E, Ponzin D, Bettio D, Salviati L, Di Iorio E. Analysis and pharmacological modulation of senescence in human epithelial stem cells. J Cell Mol Med 2022, 26: 3977-3994.
Behluli E, Nuhii N, Liehr T, Temaj G. Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with Down syndrome. J Mother Child / Medycyna Wieku Rozwojowego 2022, 26:104-110.
Capela de Matos RR, Othman M, Ferreira GM, Monteso K, de Souza MT, Rouxinol M, Melo JB, Carreira IM, Abdelhay E, Liehr T, Ribeiro RC, Silva M. Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21. Cancer Genet 2022, 262-263:16-22.
Classen S, Rahlf E, Jungwirth J, Albers N, Hebestreit LP, Zielinski A, Poole L, Groth M, Koch P, Liehr T, Kankel S, Cordes N, Petersen C, Rothkamm K, Pospiech H, Borgmann K. Partial reduction in BRCA1 gene dose modulates DNA replication stress level and thereby contributes to sensitivity or resistance. Int J Mol Sci 2022, 23:13363.
Dadyar M, Hussen BM, Eslami S, Taheri M, Emadi F, Ghafouri-Fard S, Sayad A. Expression of T cell-related lncRNAs in multiple sclerosis. Front Genet. 2022; 13: 967157.
de Oliveira TD, Bertocchi NA, Kretschmer R, de Oliveira EHC, Cioffi MB, Liehr T, Ochotorena de Freitas TR. Genomic organization of microsatellites and LINE-1-like etrotransposons: evolutionary implications for Ctenomys minutus (Rodentia: Ctenomyidae) cytotypes. Animals 2022, 12: 2091.
Deon GA, Glugoski L, Sassi FdMC, Hatanaka T, Nogaroto V, Bertollo LAC, Liehr T, Al-Rikabi A, Moreira-Filho OdB, Cioffi MdB, Vicari MR. Chromosomal rearrangements and origin of the multiple XX/XY1Y2 sex chromosome system in Harttia species (Siluriformes: Loricariidae). Front Genet 2022, 13: 877522.
Deon GA, Glugoski L, Hatanaka T, Sassi FdMC, Nogaroto V, Bertollo LAC, Liehr T, Al-Rikabi A, Moreira-Filho O, Cioffi MdB, Vicari MR. Evolutionary breakpoint regions and chromosomal remodeling in Harttia (Siluriformes: Loricariidae) species diversification. Genet Mol Biol 2022, 45: e20210170
de Souza FHS, Sassi FdMC, Ferreira PHN, Bertollo LAC, Ezaz T, Liehr T, Perez MF, Cioffi MB. Integrating cytogenetics and population genomics: Allopatry and neo-sex chromosomes shaped the genetic divergence in the Erythrinus erythrinus species complex (Teleostei, Characiformes). Biology 2022, 11: 315.
de Matos RRC, Ferreira GM, Meyer C, Marschalek R, Larghero P, Ribeiro RC, Liehr T, Othman M, Bizarro MTdeSM, Sobral da Costa E, Land MGP, Abdelhay E, Binato R, Silva MLM. KMT2A-MLLT1 and the novel SEC16A-KMT2A in a cryptic three-way translocation t(9;11;19) present in an infant with acute lymphoblastic leukemia. J Pediat Hematol Oncol 2022, 44: e719.
Dong P, Wang F, Taheri M, Xiong Y, Ihira K, Kobayashi N, Konno Y, Yue J, Watari H. Long non-coding RNA TMPO-AS1 promotes GLUT1-mediated glycolysis and paclitaxel resistance in endometrial cancer cells by interacting with miR-140 and miR-143. Front Oncol. 2022; 12: 912935.
Eck S, Fritz B, Haferlach C, Kunz J, Liehr T, Matos-Meder S, Rieder H, Schäfer D, Schanze I. Web-based external quality assessment (EQA) for genetic diagnostics provided by the German Association of Professionals for Human Genetics (BVDH). ECA newsletter 2022, 49: 2-4.
Eghtedarian R, Ghafouri-Fard S, Bouraghi H, Hussen BM, Arsang-Jang S, Taheri M. Abnormal pattern of vitamin D receptor-associated genes and lncRNAs in patients with bipolar disorder. BMC Psychiatry. 2022; 22: 178.
Eghtedarian R, Akbari M, Badrlou E, Mahmud Hussen B, Eslami S, Akhavan-Bahabadi M, Taheri M, Ghafouri-Fard S, Neishabouri SM. Assessment of expression of oxytocin-related lncRNAs in schizophrenia. Eur J Pharmacol. 2022; 932: 175205.
Ehsani M, Bartsch S, Rasa SMM, Dittmann J, Pungsrinont T, Neubert L, Huettner SS, Kotolloshi R, Schindler K, Ahmad A, Mosig AS, Adam L, Ori A, Neri F, Berndt A, Grimm MO, Baniahmad A. The natural compound atraric acid suppresses androgen-regulated neo-angiogenesis of castration-resistant prostate cancer through angiopoietin 2. Oncogene 2022; 41: 3263-3277.
El Amrani Z, Elalaoui SC, Jdioui W, Sbiti A, Ratbi I, Liehr T, Sefiani A, Natiq A. Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability. Ophthalmic Genetics 2022; 43:689-692
Ernst P, Schnöder TM, Huber N, Perner F, Jayavelu AK, Eifert T, Hsu CJ, Tubío-Santamaría N, Crodel CC, Ungelenk M, Hübner CA, Clement JH, Hochhaus A, Heidel FH. Histone demethylase KDM4C is a functional dependency in JAK2-mutated neoplasms. Leukemia. 2022; 36: 1843-1849.
Fan X, Pinthong K, de Oliveira EHC, Tanomtong A, Chen H, Weise A, Liehr T. First comprehensive characterization of Phayre’s leaf-monkey (Trachypithecus phayrei) karyotype. Front Genet 2022, 13: 841681.
Ferreira PHN de Souza FHS, de Moraes RLR, Perez M, Sassi F de MC, Viana PF, Feldberg E, Ezaz T, Liehr T, Bertollo LAC, Cioffi M de B. The genetic differentiation of Pyrrhulina (Teleostei, Characiformes) species is likely influenced by both geographical distribution and chromosomal rearrangements. Front Genet 2022, 13: 869073
Fleischmann M, Schnetzke U, Frietsch JJ, Sayer HG, Schrenk K, Hammersen J, Glaser A, Hilgendorf I, Hochhaus A, Scholl S. Impact of induction chemotherapy with intermediate-dosed cytarabine and subsequent allogeneic stem cell transplantation on the outcome of high-risk acute myeloid leukemia. J Cancer Res Clin Oncol. 2022; 148: 1481-1492.
Franzka P, Turecki G, Cubillos S, Kentache T, Steiner J, Walter M, Hübner CA, Engmann O. Altered mannose metabolism in chronic stress and depression is rapidly reversed by vitamin B12. Front Nutr. 2022; 9: 981511.
Ghafouri-Fard S, Taheri M. Response to MALAT1 polymorphisms and psoriasis risk: Correspondence. Int J Immunogenet. 2022; 49: 89.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Rashnoo F. A review on the role of PCA3 lncRNA in carcinogenesis with an especial focus on prostate cancer. Pathol Res Pract. 2022, 231: 153800.
Ghafouri-Fard S, Hussen BM, Mohaqiq M, Shoorei H, Baniahmad A, Taheri M, Jamali E. Interplay between non-coding RNAs and programmed cell death proteins. Front Oncol. 2022, 12: 808475.
Ghafouri-Fard S, Majidpoor J, Shoorei H, Hussen BM, Hadayat Jamal H, Baniahmad A, Taheri M, Mokhtari M. The interaction between non-coding RNAs and calcium binding proteins. Front Oncol. 2022; 12: 848376.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Branicki W, Taheri M, Eghbali A. Emerging role of non-coding RNAs in senescence. Front Cell Dev Biol. 2022; 10: 869011.
Ghafouri-Fard S, Taheri M, Baniahmad A. Inhibitor of growth factors regulate cellular senescence. Cancers (Basel). 2022; 14: 3107.
Ghafouri-Fard S, Abak A, Baniahmad A, Hussen BM, Taheri M, Jamali E, Dinger ME. Interaction between non-coding RNAs, mRNAs and G-quadruplexes. Cancer Cell Int. 2022; 22: 171.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Salimi A. A review on the role of PRNCR1 in human disorders with an especial focus on cancer. Pathol Res Pract. 2022 Sep;237:154026.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Dong P, Gassler N, Taheri M, Baniahmad A, Dilmaghani NA. A review on the role of cyclin dependent kinases in cancers. Cancer Cell Int. 2022; 22: 325.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Samadian M. A review on the role of DANCR in the carcinogenesis. Cancer Cell Int. 2022; 22: 194.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Mokhtari M. A review on the role of PCGEM1 lncRNA in cancer. Pathol Res Pract. 2022, 240: 154223.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Samsami M. A review on the role of NR2F1-AS1 in the development of cancer. Pathol Res Pract 2022, 240: 154210.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Baniahmad A, Taheri M, Hajiesmaeili M. A concise review on dysregulation of LINC00665 in cancers. Cells 2022, 11: 3575.
Ghafouri-Fard S, Khanbabapour Sasi A, Hussen BM, Shoorei H, Siddiq A, Taheri M, Ayatollahi SA. Interplay between PI3K/AKT pathway and heart disorders. Mol Biol Rep. 2022; 2 :1-5.
Ghafouri-Fard S, Najafi S, Hussen BM, Basiri A, Hidayat H, Taheri M, Rashnoo F. The role of circular RNAs in the carcinogenesis of bladder cancer. Front Oncol. 2022; 28: 498.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Samadian M. A review on the role of miR-1246 in the pathoetiology of different cancers. Front Mol Biosci. 2022; 8: 1233.
Ghafouri-Fard S, Shoorei H, Bahroudi Z, Hussen BM, Talebi SF, Taheri M, Ayatollahi SA. Nrf2-related therapeutic effects of curcumin in different disorders. Biomolecul. 2022; 12: 82.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Sarfaraz S, Taheri M, Ayatollahi SA. Circ_CDR1as: a circular RNA with roles in the carcinogenesis. Pathol Res Pract. 2022; 1: 153968.
Ghafouri-Fard S, Noroozi R, Brand S, Hussen BM, Eghtedarian R, Taheri M, Ebrahimzadeh K. Emerging role of non-coding RNAs in autism spectrum disorder. J Mol Neurosci. 2022; 72: 201-216.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Samsami M. Emerging role of circular RNAs in the pathogenesis of ovarian cancer. Cancer Cell Int. 2022; 22: 172.
Ghafouri-Fard S, Hussen BM, Abak A, Taheri M, Jalili Khoshnoud R. Aberrant expression of miRNAs in epilepsy. Mol Biol Rep. 2022; 49: 5057-5074.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Jamali E. The emerging role non-coding RNAs in B cell-related disorders. Cancer Cell Int. 2022; 22: 91.
Ghafouri-Fard S, Shirvani-Farsani Z, Hussen BM, Taheri M, Jalili Khoshnoud R. Emerging role of non-coding RNAs in the regulation of KRAS. Cancer Cell Int. 2022; 22: 68.
Ghafouri-Fard S, Shoorei H, Poornajaf Y, Hussen BM, Hajiesmaeili Y, Abak A, Taheri M, Eghbali A. NLRP3: Role in ischemia/reperfusion injuries. Front Immunol. 2022; 13: 926895.
Ghafouri-Fard S, Poornajaf Y, Dashti F, Hussen BM, Taheri M, Jamali E. Interaction between non-coding RNAs and interferons: with an especial focus on type I interferons. Front Immunol. 2022; 13: 877243.
Ghafouri-Fard S, Najafi S, Hussen BM, Ganjo AR, Taheri M, Samadian M. DLX6-AS1: A long non-coding RNA with oncogenic features. Front Cell Dev Biol. 2022; 10: 746443.
Ghafouri-Fard S, Hussen BM, Jamal HH, Taheri M, Sharifi G. The emerging role of non-coding RNAs in the regulation of virus replication and resultant cellular pathologies. Int J Mol Sci. 2022; 23: 815.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Hajiesmaeili M. A review on the role of LINC00467 in the carcinogenesis. Cancer Cell Int. 2022; 22: 319.
Ghafouri-Fard S, Noie Alamdari A, Noee Alamdari Y, Abak A, Hussen BM, Taheri M, Jamali E. Role of PI3K/AKT pathway in squamous cell carcinoma with an especial focus on head and neck cancers. Cancer Cell Int. 2022; 22: 254.
Ghafouri-Fard S, Askari A, Hussen BM, Taheri M, Mokhtari M. A long non-coding RNA with important roles in the carcinogenesis. Front Cell Dev Biol. 2022; 10: 1037149.
Ghafouri-Fard S, Shirvani-Farsani Z, Hussen BM, Taheri M, Samsami M. The key roles of non-coding RNAs in the pathophysiology of hypertension. Eur J Pharmacol. 2022; 931: 175220.
Ghafouri-Fard S, Balaei N, Shoorei H, Hasan SMF, Hussen BM, Talebi SF, Taheri M, Ayatollahi SA. The effects of Ginsenosides on PI3K/AKT signaling pathway. Mol Biol Rep. 2022; 49: 6701-6716.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Jamal HH, Taheri M, Hajiesmaeili M. A comprehensive review on function of miR-15b-5p in malignant and non-malignant disorders. Front Oncol. 2022; 12: 870996.
Ghafouri-Fard S, Askari A, Hussen BM, Rasul MF, Hatamian S, Taheri M, Kiani A. A review on the role of miR-671 in human disorders. Front Mol Biosci. 2022; 9: 1077968.
Ghafouri-Fard S, Gholami L, Sadeghpour S, Nazer N, Hussen BM, Sayad A, Taheri M. Altered expression of SOCS genes periodontitis. BMC Oral Health. 2022; 22: 551.
Ghafouri-Fard S, Safarzadeh A, Hussen BM, Taheri M, Rashnoo F. A concise review on the role of LINC00324 in different cancers. Pathol Res Pract. 2022; 240: 154192.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Abdullah ST, Taheri M, Samadian M. A review on the role of mir-16-5p in the carcinogenesis. Cancer Cell Int. 2022; 22: 342.
Ghafouri-Fard S, Hussen BM, Jamali E, Branicki W, Taheri M, Akbari Dilmaghani N. Role of lncRNAs and circRNAs in epilepsy. Ageing Res Rev. 2022; 82: 101749.
Ghafouri-Fard S, Bahroudi Z, Shoorei H, Hussen BM, Talebi SF, Baig SG, Taheri M, Ayatollahi SA. Disease-associated regulation of gene expression by resveratrol: Special focus on the PI3K/AKT signaling pathway. Cancer Cell Int. 2022; 22: 298.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Samsami M. Emerging role of non-coding RNAs in the regulation of Sonic Hedgehog signaling pathway. Cancer Cell Int. 2022; 22: 282.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Samsami M. miR-1908: a microRNA with diverse functions in cancers and non-malignant conditions. Cancer Cell Int. 2022; 22: 281.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Mokhtari M. A review on the role of LINC01133 in cancers. Cancer Cell Int. 2022; 22: 270.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Akbari Dilmaghani N. A review on the role of PTENP1 in human disorders with an especial focus on tumor suppressor role of this lncRNA. Cancer Cell Int. 2022; 22: 207.
Ghafouri-Fard S, Safarzadeh A, Mahmud Hussen B, Akhavan-Bahabadi M, Taheri M, Sharifi G. In silico characterization of competing endogenous RNA network in glioblastoma multiforme with a systems biology approach. Front Oncol. 2022; 12: 1024567.
Ghafouri-Fard S, Khoshbakht T, Hussen BM, Taheri M, Ebrahimzadeh K, Noroozi R. The emerging role of long non-coding RNAs, microRNAs, and an accelerated epigenetic age in Huntington's disease. Front Aging Neurosci. 2022; 14: 987174.
Ghafouri-Fard S, Poornajaf Y, Hussen BM, Abak A, Shoorei H, Taheri M, Sharifi G. Implication of non-coding RNA-mediated ROCK1 regulation in various diseases. Front Mol Biosci. 2022; 9: 986722.
Ghafouri-Fard S, Safarzadeh A, Akhavan-Bahabadi M, Hussen BM, Taheri M, Dilmaghani NA. Expression pattern of non-coding RNAs in non-functioning pituitary adenoma. Front Oncol. 2022; 12: 978016.
Ghafouri-Fard S, Hussen BM, Shaterabadi D, Abak A, Shoorei H, Taheri M, Rakhshan A. The interaction between human papilloma viruses related cancers and non-coding RNAs. Pathol Res Pract. 2022; 234: 153939.
Ghafouri-Fard S, Askari A, Hussen BM, Rasul MF, Taheri M, Kiani A. A review on the role of LINC00152 in different disorders. Pathol Res Pract. 2022; 241: 154274.
Harutyunyan T, Liehr T. Can age related mosaic loss of Y chromosome really cause cardiac damage in men? eletter (1) for Sano, et al. Science 2022, 377:292-297 - https://www.science.org/doi/10.1126/science.abn3100
Herrmann T, Gerth M, Dittmann R, Pensold D, Ungelenk M, Liebmann L, Hübner CA. Disruption of KCC2 in parvalbumin-positive interneurons is associated with a decreased seizure threshold and a progressive loss of parvalbumin-positive interneurons. Front Mol Neurosc 2022, 14:807090.
Hussen BM, Faraj GSH, Rasul MF, Hidayat HJ, Salihi A, Baniahmad A, Taheri M, Ghafouri-Frad S. Strategies to overcome the main challenges of the use of exosomes as drug carrier for cancer therapy. Cancer Cell Int. 2022; 22: 323.
Hussen BM, Abdullah ST, Salihi A, Sabir DK, Sidiq KR, Rasul MF, Hidayat HJ, Ghafouri-Fard S, Taheri M, Jamali E. The emerging roles of NGS in clinical oncology and personalized medicine. Pathol Res Pract. 2022; 10: 153760.
Hussen BM, Kheder RK, Abdullah ST, Hidayat HJ, Rahman HS, Salihi A, Taheri M, Ghafouri-Fard S. Functional interplay between long non-coding RNAs and breast CSCs. Cancer Cell Internat. 2022; 22: 1-9.
Hussen BM, Abdullah SR, Hama Faraj GS, Rasul MF, Salihi A, Ghafouri-Fard S, Taheri M, Mokhtari M. Exosomal circular RNA: a signature for lung cancer progression. Cancer Cell Int. 2022; 22: 378.
Kasiroek W, Phimphan S, Pinthong K, Suwannapoom C, Aiumsumang S, Liehr T, Supiwong W, Tanomtong A. Comparative cytogenomic analysis of cardinalfishes (Perciformes, Apogonidae) from Thailand. Nucleus 2022, 65: 57-66.
Khayamzadeh M, Niazi V, Hussen BM, Taheri M, Ghafouri-Fard S, Samadian M. Emerging role of extracellular vesicles in the pathogenesis of glioblastoma. Metab Brain Dis. 2023; 38: 177-184.
Khalifa Y, Hassan HY, Weise A, Liehr T, Alkhayyat H. Molecular cytogenetic and phenotypic characterization of Phelan McDermid and 22q13 duplication syndrome: A case report. Mol Cytogenet 2022; 15: 52.
Li P, Dupont B, Hu Q, Crimi M, Shen Y, Lebedev I, Liehr T. The past, present, and future for constitutional ring chromosomes: A report of the International Consortium for Human Ring Chromosomes (ICHRC). HGG Adv 2022, 3, 100139.
Liehr T. Uniparental disomy is a chromosomic disorder in the first place. Mol Cytogenet 2022, 15: 5.
Liehr T. Was man zu Grenzen und Möglichkeiten des Noninvasive prenatal testing (NIPT) unbedingt wissen sollte. gynäkologische praxis. 2022, 49: 425-432.
Liehr T. Was man zu Grenzen und Möglichkeiten des Noninvasive prenatal testing (NIPT) unbedingt wissen sollte. pädiatrische praxis 2022, 99: 7-14.
Liehr T. False-positives and false-negatives in non-invasive prenatal testing (NIPT): what can we learn from a meta-analyses on > 750,000 tests? Mol Cytogenet 2022, 15: 36.
Liehr T. Chromosomal heteromorphisms and cancer susceptibility revisited. Cells 2022, 11: 3239.
Liehr T, Weise A, Person L, Padutsch N, Kankel S. How to obtain high quality metaphase spreads for molecular cytogenetics. Current Protocols 2022, 2:e392.
Liehr T, Harutyunyan T, Williams H, Weise A. Non-invasive prenatal testing in Germany. Diagnostics 2022, 12: 2816.
Liehr T, Harutyunyan T, Williams H, Weise A. Restrictions and advantages of non-invasive prenatal testing (NIPT). Encylopedia 2022: 38834. https://encyclopedia.pub/entry/38834
Lischka A, Lassuthova P, Çakar A, Record CJ, Van Lent J, Baets J, Dohrn MF, Senderek J, Lampert A, Bennett DL, Wood JN, Timmerman V, Hornemann T, Auer-Grumbach M, Parman Y, Hübner CA, Elbracht M, Eggermann K, Geoffrey Woods C, Cox JJ, Reilly MM, Kurth I. Genetic pain loss disorders. Nat Rev Dis Primers. 2022; 8: 41.
Marrone L, Marchi PM, Webster CP, Marroccella R, Coldicott I, Reynolds S, Alves-Cruzeiro J, Yang ZL, Higginbottom A, Khundadze M, Shaw PJ, Hübner CA, Livesey MR, Azzouz M. SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. Hum Mol Genet. 2022; 31: 2693-2710.
Maul A, Huebner AK, Strenzke N, Moser T, Rübsamen R, Jovanovic S, Hübner CA. The Cl--channel TMEM16A is involved in the generation of cochlear Ca2+ waves and promotes the refinement of auditory brainstem networks in mice. Elife 2022; 11: e72251.
Méndez-Rosado LA, de León-Ojeda N, García A, Sheth F, Gaadi A, Bousfiha AA, Lehlimi M, Natiq A, Kurinnaia OS, Vorsanova SG, Iourov I, Huhle D, Liehr T. Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic background. Egypt J Med Hum Genet 2022, 23: 158.
Mirzakhani K, Kallenbach J, Rasa SMM, Ribaudo F, Ungelenk M, Ehsani M, Gong W, Gassler N, Leeder M, Grimm MO, Neri F, Baniahmad A. The androgen receptor-lncRNASAT1-AKT-p15 axis mediates androgen-induced cellular senescence in prostate cancer cells. Oncogene 2022; 41: 943-959. Erratum in: Oncogene 2022 41: 1071-1077.
Moallemi-Rad L, Ghorbani A, Dadyar M, Hussen BM, Rasul MF, Eslami S, Taheri M, Jamali E, Ghafouri-Fard S. Expression of Treg-associated lncRNAs in breast cancer. Pathol Res Pract. 2022; 241: 154270.
Mohanty P, Shetty D, Liehr T, Mrasek K, Khattry N. Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changes. Int J Lab Hematol 2022, 44: 993-994.
Mühleck R, Scholl S, Hilgendorf I, Schrenk K, Hammersen J, Frietsch JJ, Fleischmann M, Sayer HG, Glaser A, Hochhaus A, Schnetzke U. Outcome of patients with relapsed or refractory acute myeloid leukemia treated with Mito-FLAG salvage chemotherapy. J Cancer Res Clin Oncol 2022; 148: 2539-2548.
Najafi S, Ghafouri-Fard S, Hussen BM, Jamal HH, Taheri M, Hallajnejad M. Oncogenic roles of small nucleolar RNA host gene 7 (SNHG7) long noncoding RNA in human cancers and potentials. Front Cell Develop Biol 2022; 9:3734.
Nilius-Eliliwi V, Tembrink M, Gerding WM, Lubieniecki KP, Lubieniecka JM, Kankel S, Liehr T, Mika T, Dimopoulos F, Döhner K, Schroers R, Nguyen HHP, Vangala DB. Broad genomic workup including optical genome mapping uncovers a DDX3X::MLLT10 gene fusion in acute myeloid leukemia. Front Oncol 2022, 12: 959243
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Paneque M, Liehr T, Serra-Juhe C, Moog U, Melegh B, Carreira I. The need for recognition of core professional groups in genetics healthcare services in Europe. Europ J Hum Genet 2022; 30: 639-640.
Paneque M, Serra Juhé C, Melegh B, Carreira I, Moog U, Liehr T. Über die Notwendigkeit der Anerkennung von sog. Kernberufsgruppen innerhalb der genetischen Gesundheitsversorgung in Europa. Med Gen 2022, 34: 81-83. correction under 34: 189-191.
Pilz RA, Skowronek D, Hamed M, Weise A, Mangold E, Radbruch A, Pietsch T, Felbor U, Rath M. Using CRISPR/Cas9 genome editing in human iPSCs for deciphering the pathogenicity of a novel CCM1 transcription start site deletion. Front Mol Biosci. 2022, 9: 953048.
Poos AM, Schroeder C, Jaishankar N, Röll D, Oswald M, Meiners J, Braun DM, Knotz C, Frank L, Gunkel M, Spilger R, Wollmann T, Polonski A, Makrypidi-Fraune G, Fraune C, Graefen M, Chung I, Stenzel A, Erfle H, Rohr K, Baniahmad A, Sauter G, Rippe K, Simon R, Koenig R. PITX1 is a regulator of TERT expression in prostate cancer with prognostic power. Cancers (Basel). 2022, 14:1267.
Rad LM, Yumashev AV, Hussen BM, Jamad HH, Ghafouri-Fard S, Taheri M, Rostami S, Niazi V, Hajiesmaeili M. Therapeutic potential of microvesicles in cell therapy and regenerative medicine of ocular diseases with an especial focus on mesenchymal stem cells-derived microvesicles. Front Genet. 2022; 13: 847679.
Rakhshan A, Gholipour M, Hussen BM, Taheri M, Eslami S, Ghafouri-Fard S, Hafez AA. Expression analysis of CDKN2C-related lncRNAs in breast cancer. Hum Gene. 2022; 33: 201070.
Rasul MF, Hussen BM, Salihi A, Ismael BS, Jalal PJ, Zanichelli A, Jamali E, Baniahmad A, Ghafouri-Fard S, Basiri A, Taheri M. Strategies to overcome the main challenges of the use of CRISPR/Cas9 as a replacement for cancer therapy. Mol Cancer. 2022, 21:64.
Refisch A, Komatsuzaki S, Ungelenk M, Chung HY, Schumann A, Schilling SS, Jantzen W, Schröder S, Mühleisen TW, Nöthen MM, Hübner CA, Bär KJ. Associations of common genetic risk variants of the muscarinic acetylcholine receptor M2 with cardiac autonomic dysfunction in patients with schizophrenia. World J Biol Psychiatry 2022, 17: 1-35.
Refisch A, Komatsuzaki S, Ungelenk M, Schumann A, Chung HY, Schilling SS, Jantzen W, Schröder S, Nöthen MM, Mühleisen TW, Hübner CA, Bär KJ. Analysis of CACNA1C and KCNH2 Risk Variants on Cardiac Autonomic Function in Patients with Schizophrenia. Genes (Basel) 2022, 13: 2132.
Sabaie H, Talebi M, Gharesouarn J, Asadi MR, Jalaiei A, Arsang-Jang S, Hussen BM, Taheri M, Jalili Khoshnoud R, Rezazadeh M. Identification and Analysis of BCAS4/hsa-miR-185-5p/SHISA7 competing endogenous RNA axis in late-onset Alzheimer's disease using bioinformatic and experimental approaches. Front Aging Neurosci. 2022; 14: 812169.
Sabaie H, Gholipour M, Asadi MR, Abed S, Sharifi-Bonab M, Taheri M, Hussen BM, Brand S, Neishabouri SM, Rezazadeh M. Identification of key long non-coding RNA-associated competing endogenous RNA axes in Brodmann Area 10 brain region of schizophrenia patients. Front Psychiatry. 2022; 13: 1010977.
Sabaie H, Khorami Rouz S, Kouchakali G, Heydarzadeh S, Asadi MR, Sharifi-Bonab M, Hussen BM, Taheri M, Ayatollahi SA, Rezazadeh M. Identification of potential regulatory long non-coding RNA-associated competing endogenous RNA axes in periplaque regions in multiple sclerosis. Front Genet. 2022; 13: 1011350.
Safarzadeh A, Akhavan-Bahabadi M, Hussen BM, Nicknam A, Eslami S, Pouresmaeili F, Ghafouri-Fard S, Taheri M. Expression analysis of autophagy-related long non-coding RNAs in Iranian patients with breast cancer. Pathol Res Pract. 2022; 239: 154146.
Samsami M, Fatemi A, Jalili Khoshnoud R, Kohansal K, Hussen BM, Soghala S, Taheri M, Ghafouri-Fard S. Abnormal transcript levels of cytokines among Iranian COVID-19 patients. J Mol Neurosci. 2022; 72: 27-36.
Sayad A, Najafi S, Hussen BM, Jamali E, Taheri M, Ghafouri-Fard S. The role of circular RNAs in pancreatic cancer; new players in tumorigenesis and potential biomarkers. Pathol Res Pract. 2022; 2: 153833.
Sayad A, Najafi S, Hussen BM, Abdullah ST, Movahedpour A, Taheri M, Hajiesmaeili M. The emerging roles of the β-Secretase BACE1 and the long non-coding RNA BACE1-AS in human diseases: A focus on neurodegenerative diseases and cancer. Front Aging Neurosci. 2022; 14: 853180.
Schomann T, Mirzakhani K, Kallenbach J, Lu J, Rasa SMM, Neri F, Baniahmad A. Androgen-induced MIG6 regulates phosphorylation of retinoblastoma protein and AKT to counteract non-genomic AR signaling in prostate cancer cells. Biomolecules. 2022; 12: 1048.
Shariatzadeh S, Moghimi N, Khalafi F, Shafiee S, Mehrabi M, Ilkhani S, Tosan F, Nakhaei P, Alizadeh A, Varma RS, Taheri M. Metallic nanoparticles for the modulation of tumor microenvironment; A new horizon. Front Bioeng Biotechnol. 2022; 10: 847433.
Soghala S, Harsiny K, Momeni P, Hatami M, Kholghi Oskooei V, Hussen BM, Taheri M, Ghafouri-Fard S. Down-regulation of LINC-ROR, HOXA-AS2 and MEG3 in gastric cancer. Heliyon. 2022; 8: e11155.
Souche E, Beltran S, Brosens E, Belmont JW, Fossum M, Riess O, Gilissen C, Ardeshirdavani A, Houge G, van Gijn M, Clayton-Smith J, Synofzik M, de Leeuw N, Deans ZC, Dincer Y, Eck SH, van der Crabben S, Balasubramanian M, Graessner H, Sturm M, Firth H, Ferlini A, Nabbout R, De Baere E, Liehr T, Macek M, Matthijs G, Scheffer H, Bauer P, Yntema HG, Weiss MM. Recommendations for whole genome sequencing in diagnostics for rare diseases. Europ J Hum Genet 2022, 30: 1017-1021.
Spahiu L, Behluli E, Hadziselimovic R, Liehr T, Temaj G. Pathogenesis and therapy in polycystic kidney disease. Acta Medica Mediter 2022, 38: 3001-3009.
Taheri M, Ghafouri-Fard S, Najafi S, Kallenbach J, Keramatfar E, Atri Roozbahani G, Heidari Horestani M, Hussen BM, Baniahmad A. Hormonal regulation of telomerase activity and hTERT expression in steroid-regulated tissues and cancer. Cancer Cell Int. 2022; 22: 258.
Taheri M, Hussen BM, Najafi S, Abak A, Ghafouri-Fard S, Samsami M, Baniahmad A. Molecular mechanisms of inhibitor of growth (ING) family members in health and malignancy. Cancer Cell Int. 2022; 22: 272.
Taheri M, Roustapour S, Gholipour M, Hussen BM, Eslami S, Ghafouri-Fard S, Sayad A. Analysis of expression of regulatory T cell related lncRNAs in inflammatory demyelinating polyneuropathies. Int Immunopharmacol. 2022; 112: 109188.
Teshnizi SA, Shahani P, Taheri M, Hussen BM, Eslami S, Sadeghzadeh Z, Ghafouri-Fard S, Sayad A. Expression analysis of NF-ƙB-related long non-coding RNAs in bipolar disorder. Sci Rep. 2022; 12: 20941.
Tóth K, Lénárt N, Berki P, Fekete R, Szabadits E, Pósfai B, Cserép C, Alatshan A, Benkő S, Kiss D, Hübner CA, Gulyás A, Kaila K, Környei Z, Dénes Á. The NKCC1 ion transporter modulates microglial phenotype and inflammatory response to brain injury in a cell-autonomous manner. PLoS Biol 2022; 20: e3001526.
Wafa A, Ali B, Moassass F, Kheder M, Aljapawe A, AL-Halabi B, Mrasek K, Liehr T, Al-Achkar W. Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family. Mol Genet Genomic Med 2022, 10: e1854.
Wang Y, Kumar KR, Liehr T. Molecular combing and its application in clinical settings. Mol Cytogenet 2022, 15: 50.
Weber A, Liehr T, Al-Rikabi A, Bilgen S, Heinrich U, Schiller J, Stumm M. The first neocentric, discontinous, and complex small supernumerary marker chromosome composed of 7 euchromatic blocks derived from 5 different chromosomes. Biomedicines 2022, 10: 1102.
Zywitza V, Frahm S, Krüger N, Weise A, Göritz F, Hermes R, Holtze S, Colleoni S, Galli C, Drukker M, Hildebrandt TB, Diecke S. Induced pluripotent stem cells and cerebral organoids from the critically endangered Sumatran rhinoceros. iScience 2022, 25: 105414.