2024

• Afif L, El Amrani Z, Sbiti A, Ratbi I, Jaouad IC, El Kadiri Y, Liehr T, Sefiani A, Natiq A. First female patient with de novo 6q22.31q27 duplication and Xq28 deletion: case report and brief literature review. OBM Genetics 2024, 8:259
• Alemi F, Poornajaf Y, Hosseini F, Vahedian V, Gharekhani M, Shoorei H, Taheri M. Interaction between lncRNAs and RNA-binding proteins (RBPs) influences DNA damage response in cancer chemoresistance. Mol Biol Rep 2024; 51:308.
• Ariffen NA , Ornellas AA, Alves G, Shana'ah AM, Sharma S, Kankel S, Jamali E, Theis B, Liehr T. Amplification of different satellite-DNAs in prostate cancer. Pathol Res Pract 2024, 256: 155269.
• Asadi MR, Gharesouran J, Sabaie H, Zaboli Mahdiabadi M, Mazhari SA, Sharifi-Bonab M, Shirvani-Farsani Z, Taheri M, Sayad A, Rezazadeh M. Neurotrophin growth factors and their receptors as promising blood biomarkers for Alzheimer's Disease: a gene expression analysis study. Mol Biol Rep 2024; 51:49. 
• Atri Roozbahani G, Kokal-Ribaudo M, Heidari Horestani M, Pungsrinont T, Baniahmad A. The protein composition of exosomes released by prostate cancer cells is distinctly regulated by androgen receptor-antagonists and -agonist to stimulate growth of target cells. Cell Commun Signal 2024; 22:219. 
• Bekhite MM, Hübner S, Kretzschmar T, Backsch C, Weise A, Klein E, Bogoviku J, Westphal J, Christian Schulze P. Generation of human induced pluripotent stem cell lines UKJi001-A and UKJi006-A from patients with heterozygous mutation in the PKP2 gene. Stem Cell Res 2024, 81:103565. 
• Bertrand M, Shah G, Pedersen BS, Schulz A, Weise A, Liehr T, Huppke P, DiTroia S, Quinlan AR, Haack TB, Husain RA. De novo AHDC1 deletions identified by genome sequencing in two individuals with Xia-Gibbs syndrome. Mol Syndromol 2024, 15:389-397. 
• Buasriyot P, Sassi FMC, Donbundit N, Supiwong W, Kaewsri S, Jumrusthanasan S, Suwannapoom C, Pinthong K, Tanomtong A, Yanukun K, Tantisuwichwong N, Muanglen N, Liehr T, Cioffi MB. Comparative karyotypic study of fifteen cyprinids (Cyprinidae, Cyprininae) species. An insight into the chromosomal evolution of the tribe Systomini. PLoS One 2024, 19: e0305828.
• Dini N, Taheri M, Shirvani-Farsani Z. The expression analysis of long noncoding RNAs PCAT-1, PCAT-29, and MER11C in bipolar disorder. BMC Psychiatry 2024, 24:524.
• El Amrani Z, Natiq A, Sbiti A, Ratbi I, Liehr T, Sefiani A, Sahli M. Currarino syndrome in two Moroccan siblings with inherited 7q36 deletion due to maternal t(7;21)(q36;p11)mat: A case report. Mol Syndromol 2024, 15:125-129.
• Esmaeili Motlagh P, Ghafouri-Fard S, Eslami S, Sharifi G, Taheri M. Expression assays of selected lncRNAs in non-functioning pituitary adenomas. Discov Oncol 2024, 15:486. 
• Fontes ALT, Padutsch N, Kankel S, Liehr T. Molecular cytogenetic characterization of rare, but repeatedly observed translocations. OBM Genetics 2024, 8:240.
• Franzka P, Mittag S, Chakraborty A, Huber O, Hübner CA. Ubiquitination contributes to the regulation of GDP-mannose pyrophosphorylase B activity. Front Mol Neurosci 2024, 17:1375297. 
• Ghafouri-Fard S, Askari A, Shoorei H, Seify M, Koohestanidehaghi Y, Hussen BM, Taheri M, Samsami M. Antioxidant therapy against TGF-β/SMAD pathway involved in organ fibrosis. J Cell Mol Med 2024; 28:e18052. 
• Ghamari M, Mehrab Mohseni M, Taheri M, Neishabouri SM, Shirvani-Farsani Z. Abnormal expression of long non-coding RNAs RMRP, CTC-487M23.5, and DGCR5 in the peripheral blood of patients with Bipolar disorder. Metab Brain Dis 2024; 39:313-320. 
• Gharesouran J, Hosseinzadeh H, Ghergherechi R, Shiva S, Taheri M, Liehr T, Rezazadeh M. Loss of helicase C-terminal domain of SMARCAL1 protein associated with severe Schimke immuno-osseous dysplasia. Pathol Res Pract 2024, 254: 155092.
• Gorodetska I, Offermann A, Püschel J, Lukiyanchuk V, Gaete D, Kurzyukova A, Freytag V, Haider MT, Fjeldbo CS, Di Gaetano S, Schwarz FM, Patil S, Borkowetz A, Erb HHH, Baniahmad A, Mircetic J, Lyng H, Löck S, Linge A, Lange T, Knopf F, Wielockx B, Krause M, Perner S, Dubrovska A. ALDH1A1 drives prostate cancer metastases and radioresistance by interplay with AR- and RAR-dependent transcription. Theranostics 2024, 14:714-737. 
• Graiqevci-Uka V, Behluli E, Hadziselimovic R, Liehr T, Temaj G. Implementation of pharmacogenetics for treatment of patients with acute lymphoblastic leukemia. Res Results Pharmacol 2024, 10:27-39.
• Hama Faraj GS, Hussen BM, Abdullah SR, Fatih Rasul M, Hajiesmaeili Y, Baniahmad A, Taheri M. Advanced approaches of the use of circRNAs as a replacement for cancer therapy. Noncoding RNA Res 2024; 9:811-830. 
• Harutyunyan T, Sargsyan A, Kalashyan L, Igityan H, Grigoryan B, Davtyan H, Aroutiounian R, Liehr T, Hovhannisyan G. Changes in telomere length in leukocytes and leukemic cells after ultrashort electron beam radiation. IJMS 2024, 25: 6709. 
• Harutyunyan T, Sargsyan A, Kalashyan L, Stepanyan N, Aroutiounian R, Liehr T, Hovhannisyan G. DNA damage in moderate and severe COVID-19 cases: Relation to demographic, clinical, and laboratory parameters.IJMS 2024, 25: 10293.
• Harsij A, Gharebaghi A, Ghiasian M, Eslami S, Ghafouri-Fard S, Taheri M, Sayad A. Expression analysis of Treg-related lncRNAs in neuromyelitis optica spectrum disorder. Mult Scler Relat Disord 2024; 81:105350.
• Heidari Horestani M, Atri Roozbahani G, Baniahmad A. The clock gene BHLHE40 and atypical CCNG2 control androgen-induced cellular senescence as a novel tumor suppressive pathway in prostate cancer. J Exp Clin Cancer Res 2024, 43:174. 
• Hospodářská M, Mora P, Voleníková AC, Al-Rikabi A, Simanovsky SA, Pavlica T, Altmanová M,Janečková K, Štundlová J, Tolar N, Jankásek M, Hiřman M, Liehr T, Reichard M, Krysanov EY, Ráb P, Englert C, Nguyen P, Sember A. Sex chromosome turnover in African annual killifishes of the genus Nothobranchius. bioRxiv 2024, doi: https://doi.org/10.1101/2024.03.25.586567
• Husain RA, Jiao X, Hennings JC, Giesecke J, Palsule G, Beck-Wödl S, Osmanović D, Bjørgo K, Mir A, Ilyas M, Abbasi SM, Efthymiou S, Dominik N, Maroofian R, Houlden H, Rankin J, Pagnamenta AT, Nashabat M, Altwaijri W, Alfadhel M, Umair M, Khouj E, Reardon W, El-Hattab AW, Mekki M, Houge G, Beetz C, Bauer P, Putoux A, Lesca G, Sanlaville D, Alkuraya FS, Taylor RW, Mentzel HJ, Hübner CA, Huppke P, Hart RP, Haack TB, Kiledjian M, Rubio I. Biallelic NUDT2 variants defective in mRNA decapping cause a neurodevelopmental disease. Brain 2024; 147:1197-1205. 
• Hussen BM, Najmadden ZB, Abdullah SR, Rasul MF, Mustafa SA, Ghafouri-Fard S, Taheri M. CRISPR/Cas9 gene editing: a novel strategy for fighting drug resistance in respiratory disorders. Cell Commun Signal 2024, 22:329.
• Hussen BM, Abdullah SR, Mohammed AA, Rasul MF, Hussein AM, Eslami S, Glassy MC, Taheri M. Advanced strategies of targeting circular RNAs as therapeutic approaches in colorectal cancer drug resistance. Pathol Res Pract 2024, 260:155402. 
• Hyckel P, Liehr T. Thoughts on the etiology of cherubism. J Clin Med 2024, 13: 2082.
• Israel JS, Marcelin LM, Thomas C, Szczyrbová E, Fuessel S, Puhr M, Linxweiler J, Yalala S, Zwart WT, Baniahmad A, van Goubergen J, Itkonen HM, Sharp A, O'Neill E, Pretze M, Miederer M, Erb HHH. Emerging frontiers in androgen receptor research for prostate Cancer: insights from the 2nd international androgen receptor Symposium. J Exp Clin Cancer Res 2024, 43:194. 
• Jedraszak G, Jobic F, Receveur A, Bilan F, Gilbert-Dussardier B, Tiffany B, Missirian C, Willems M, Odent S, Lucas J, Dubourg C, Schaefer E, Scheidecker S, Lespinasse J, Goldenberg A, Guerrot AM, Joly-Helas G, Chambon P, Le Caignec C, David A, Coutton C, Satre V, Vieville G, Amblard F, Harbuz R, Sanlaville D, Till M, Vincent-Delorme C, Colson C, Andrieux J, Naudion S, Toutain J, Rooryck C, de Fréminville B, Prieur F, Daire VC, Amram D, Kleinfinger P, Schulze MB, Raabe-Meyer G, Courage C, Lemke J, Stefanou EG, Loretta T, Emmanouil M, Tzeli SK, Sodowska H, Anderson J, Nandini A, Copin H, Garçon L, Liehr T, Morin G. Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases. Am J Med Genet A 2024, 194:e63476.
• Keramida C, Papoulidis I, Pappa E, Liehr T, Kalmantis K, Gerede A, Pavlidou E, Petersen MB, Manolakis E. An asymptomatic male individual carrying a 5.72 Mb de novo deletion in 8p23.2‑p23.3: A case report. Exp Therap Med 2024, 27:241.
• Kheder RK, Darweesh O, Hussen BM, Abdullah SR, Basiri A, Taheri M. Mesenchymal stromal cells (MSCs) as a therapeutic agent of inflammatory disease and infectious COVID-19 virus: live or dead mesenchymal? Mol Biol Rep 2024; 51:295. 
• Khensuwan S, de Menezes Cavalcante Sassi F, Rosa de Moraes RL, Rab P, Liehr T, Supiwong W, Seetapan K, Tanomtong A, Tantisuwichwong N, Arunsang S, Buasriyot P, Tongnunui S, Cioffi MB. Chromosomes of Asian cyprinid fishes: Novel insight into the chromosomal evolution of Labeoninae (Teleostei, Cyprinidae). PLoS One 2024, 19(2):e0292689. 
• Kretschmer R, Toma GA, Deon GA, dos Santos N, dos Santos RZ, Utsunomia R, Porto-Foresti F, Gunski RJ, Del Valle Garnero A, Liehr  T, de Oliveira EHC, Ochotorena de Freitas TR, de Bello Cioffi M. Satellitome analysis in the southern lapwing (Vanellus chilensis) genome: Implications for SatDNA evolution in Charadriiform birds. Genes 2024, 15:258.
• Krumm L, Pozner T, Zagha N, Coras R, Arnold P, Tsaktanis T, Scherpelz K, Davis MY, Kaindl J, Stolzer I, Süß P, Khundadze M, Hübner CA, Riemenschneider MJ, Baets J, Günther C, Jayadev S, Rothhammer V, Krach F, Winkler J, Winner B, Regensburger M. Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients. Acta Neuropathol 2024, 147:28.
• Liehr T. Editorial: Co-occurrence of numerical and structural aberration—small supernumerary marker chromosomes and B-chromosomes. Front Genet 2024, 14:1408674.
• Liehr T.  Noninvasive prenatal testing (NIPT) results are less accurate the later applied during pregnancy. Taiw J Obstet Gynecol 2024, 63: 892-895.
• Llamos-Paneque A, Echevarria-Frutos I, León-Siosa A, Herrmann T, Liehr T. Becker phenotype muscular dystrophy in a man with Klinefelter syndrome: a rare association. OBM-Genetics 2024, 8: 262.

• Makowska A, Kontny U, Liehr T, Weiskirchen R. The struggle continues: Cell misidentification. Lab Investig 2024, 104:102124.

• Manzolillo A, Gresing L, Hübner CA, Franzka P. Knockdown of INPP5K compromises the differentiation of N2A cells. Front Mol Neurosci 2024; 17:1356343. 
• Maroofian R, Zamani M, Kaiyrzhanov R, Liebmann L, Karimiani EG, Vona B, Huebner AK, Calame DG, Misra VK, Sadeghian S, Azizimalamiri R, Mohammadi MH, Zeighami J, Heydaran S, Toosi MB, Akhondian J, Babaei M, Hashemi N, Schnur RE, Suri M, Setzke J, Wagner M, Brunet T, Grochowski CM, Emrick L, Chung WK, Hellmich UA, Schmidts M, Lupski JR, Galehdari H, Severino M, Houlden H, Hübner CA. Biallelic variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder. Genet Med 2024; 26:101034.
• Maroofian R, Sarraf P, O'Brien TJ, Kamel M, Cakar A, Elkhateeb N, Lau T, Patil SJ, Record CJ, Horga A, Essid M, Selim L, Benrhouma H, Ben Younes T, Zifarelli G, Pagnamenta AT, Bauer P, Khundadze M, Mirecki A, Kamel SM, Elmonem MA, Ghayoor Karimiani E, Jamshidi Y, Offiah AC, Rossor AM, Youssef-Turki IB, Hübner CA, Munot P, Reilly MM, Brown AEX, Nagy S, Houlden H. RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity. Brain 2024, 147:2334-2343.

• Moch J, Radtke M, Liehr T, Eggermann T, Gilissen C, Pfundt R, Astuti G, Hentschel J, Schumann I. Automatized detection of uniparental disomies in a large cohort. Hum Genet 2024, 142: 955-964.

• Mokhtaridoost M, Chalmers J, Soleimanpoor M, McMurray B, Lato D, Nguyen SC, Musienko V, Nash J, Espeso-Gil S, Ahmed S, Delfosse K, Browning J, Barutcu A, Wilson M, Liehr T, Shlien A, Aref S, Joyce E, Weise A, Maass P. Inter-chromosomal contacts demarcate genome topology along a spatial gradient. Nature Comunicat 2024; 15: 9813.

• Molina WF, Khensuwan S, de Moraes RLR, Sassi FdMC, da Costa GWWF , Miguel DZ, Supiwong W, Jantarat S, Phintong K, Seetapan K, Ditcharoen S, Tanomtong A, Liehr T, Cioffi MdB. Karyotypic stasis and its implications for extensive hybridization events in corallivores species of butterflyfishes (Chaetodontidae). Heliyon 2024, 10: e27435.
• Montjean D, Beaumont M, Natiq A, Louanjli N, Hazout A, Miron P, Liehr T, Cabry R, Ratbi I, Benkhalifa M. Genome and epigenome disorders and male infertility: Feedback from 15 years of clinical and research experience. Genes 2024, 15: 377.

• Nikitin PA, Sidorov S, Liehr T, Klimina K, Al-Rikabi A, Korchagin V, Kolomiets O, Arakelyan M, Spangenberg V. Variants of a major DNA satellite discriminate parental subgenomes in a hybrid parthenogenetic lizard Darevskia unisexualis (Darevsky, 1966). JEZ-B 2024, 342:368-379.

• Ouboukss F, El Amrani Z, Bouchahta H, Ratbi I, Sbiti A, Liehr T, Sefiani A, Natiq A. A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature. Front Genet 2024, 15:1331676.

• Pires S, Jorge P, Liehr T, Oliva-Teles N. The challenge of classifying human chromosomal heteromorphisms by banding cytogenetics: from the controversial guidelines to the need of a universal scoring system. Hum Genome Var 2024, 11:38.

• Pourtavakoli A, Ghafouri-Fard S, Eslami S, Brand S, Taheri M. Expression assay of calcium signaling related lncRNAs in autism. Mol Biol Rep 2024, 51:185. 
• Rauch E, Amendt T, Lopez Krol A, Lang FB, Linse V, Hohmann M, Keim AC, Kreutzer S, Kawengian K, Buchholz M, Duschner P, Grauer S, Schnierle B, Ruhl A, Burtscher I, Dehnert S, Kuria C, Kupke A, Paul S, Liehr T, Lechner M, Schnare M, Kaufmann A, Huber M, Winkler TH, Bauer S, Yu P. T-bet+ B cells are activated by and control endogenous retroviruses through TLR-dependent mechanisms. Nat Commun 2024, 15:1229. 
• Sales‑Oliveira VC, dos Santos RZ, Goes CAG, Calegari RM, Garrido‑Ramos MA, Altmanová M, Ezaz T, Liehr T, Porto‑Foresti F, Utsunomia R, Cioffi MB. Evolution of ancient satellite DNAs in extantalligators and caimans (Crocodylia, Reptilia). BMC Biology 2024, 22:47.
• Schurig MK, Umeh O, Henze H, Jung MJ, Gresing L, Blanchard V, von Maltzahn J, Hübner CA, Franzka P. Consequences of GMPPB deficiency for neuromuscular development and maintenance. Front Mol Neurosci 2024, 17:1356326. 

• Seixas J, Padutsch N, Kankel S, Liehr T, Sy A. Molecular cytogenetic characterization of rare, but repeatedly observed inversions in German population. Cytogenet Genome Res 2024, 164:78-84.

• Setti PG, Deon GA, dos Santos RZ, Goes CAG, Garnero ADV, Gunski RJ, de Oliveira EHC, Porto-Foresti F, de Freitas TRO, Silva FAO, Liehr T, Utsunomia R, Kretschmer R, Cioffi MdB. Evolution of bird sex chromosomes: a cytogenomic approach in Palaeognathae species. BMC Ecol Evol 2024, 24:51

• Souza GM, Kretschmer R, Toma GA, de Oliveira AM, Deon GA, Setti PG, Zeni Dos Santos R, Goes CAG, Del Valle Garnero A, Gunski RJ, de Oliveira EHC, Porto-Foresti F, Liehr T, Utsunomia R, de Bello Cioffi M. Satellitome analysis on the pale-breasted thrush Turdus leucomelas (Passeriformes; Turdidae) uncovers the putative co-evolution of sex chromosomes and satellite DNAs. Sci Rep 2024, 14:20656. 
• Taheri M, Shirvani-Farsani Z, Harsij A, Fathi M, Khalilian S, Ghafouri-Fard S, Baniahmad A. A review on the role of KCNQ1OT1 lncRNA in human disorders. Pathol Res Pract 2024, 255:155188. 
• Taheri M, Eghtedarian R, Eslami S, Hussen BM, Ghafouri-Fard S, Ayatollahi SA. Alteration in the expression of long non-coding RNAs in the circulation of migraineurs. Acta Neurol Belg 2024, 124:1295-1301. 
• Taheri M, Safarzadeh A, Baniahmad A. Unveiling four axes ADAMTS9-AS2|MEG3/hsa-miR-150/PRKCA|MMP14 within prostate cancer through establishment of the ceRNA network. Pathol Res Pract 2024, 263:155604.

• Toma GA, Sember A, Goes CAG, Kretschmer R, Porto‑Foresti F, Bertollo LAC, Liehr T, Utsunomia R, Cioffi MdB. Satellite DNAs and the evolution of the multiple X1X2Y sex chromosomes in the wolf fish Hoplias malabaricus (Teleostei; Characiformes). Scientific Rep 2024; 14:20402.

• Weiskirchen R, Kankel S, Liehr T. Short tandem repeat profile for authentication of immortal murine cancer cell line MH-22A. Cell Tissue Biol, 2024, 18: 273-279.

Bücher/ Books