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Fake Peer Review and Inappropriate Authorship Are Real Evils
Horacio Rivera 대한의학회 2019 Journal of Korean medical science Vol.34 No.2
Inappropriate authorship and other fraudulent publication strategies are pervasive. Here, I deal with contribution disclosures, authorship disputes versus plagiarism among collaborators, kin co-authorship, gender bias, authorship trade, and fake peer review (FPR). In contrast to underserved authorship and other ubiquitous malpractices, authorship trade and FPR appear to concentrate in some Asian countries that exhibit a mixed academic patter of rapid growth and poor ethics. It seems that strong pressures to publish coupled with the incessantly growing number of publications entail a lower quality of published science in part attributable to a poor, compromised or even absent (in predatory journals) peer review. In this regard, the commitment of Publons to strengthen this fundamental process and ultimately ensure the quality and integrity of the published articles is laudable. Because the many recommendations for adherence to authorship guidelines and rules of honest and transparent research reporting have been rather ineffective, strong deterrents should be established to end manipulated peer review, undeserved authorship, and related fakeries.
Alma Laura Sánchez-Casillas,Horacio Rivera,Anna Gabriela Castro-Martínez,José Elías García-Ortiz,Carlos Córdova-Fletes,Paul Mendoza-Pérez 대한진단검사의학회 2017 Annals of Laboratory Medicine Vol.37 No.1
Dear Editor, The rec(8)dup(8q)inv(8)(p23.1q22.1) chromosome associated with San Luis Valley Syndrome (SLVS OMIM 179613) is usually diagnosed in Hispanic patients from the USA Southwest where a founder carrier Spaniard lived around 1800 [1, 2]. This rec(8) has an 8q duplication of 47.90 Mb and an 8p deletion of 11.65 Mb [3, 4]. Excluding two de novo rec(8)dup q chromosomes characterized only by G-bands and included in a recent compilation [5], cytogenomic analyses identified nine comparable de novo der(8)dup q/del p chromosomes with or without a simultaneous 8p gain. We describe a Mexican mestizo girl with a de novo SLVS-like der(8) but with a concomitant 8p22p23.1 duplication.
A Girl with 15q Overgrowth Syndrome and dup(15)(q24q26.3) that Included Telomeric Sequences
María de los Ángeles Gutiérrez-Franco,María de la Luz Madariaga-Campos,Ana I. Vásquez-Velásquez,Esmeralda Matute,Roberto Guevara-Yáñez,Horacio Rivera 대한진단검사의학회 2010 Annals of Laboratory Medicine Vol.30 No.3
Distal 15q trisomy or tetrasomy is associated with a characteristic phenotype that includes mild to moderate intellectual disability, abnormal behavior, speech impairment, overgrowth, hyperlaxity, long face, prominent nose, puffy cheeks, pointed chin, small ears, and hand anomalies (mainly arachno- and camptodactyly). We present the case of a 13-yr-old girl with the main clinical features of 15q overgrowth syndrome and a 46,XX,dup(15)(q24q26.3)[117]/46,XX[3].ish dup(15)(q24q26.3) (SNPRN+,PML+,subtel++,tel++) de novo karyotype. The findings in this case are consistent with those in the previous distal 15q trisomy cases that presented with overgrowth and mental retardation. Further, the rearranged chromosome had a double set of directly oriented telomeric and subtelomeric sequences. (Korean J Lab Med 2010;30:318-24)