A Rare Case of Severe Congenital RYR1-Associated Myopathy by Nicola Laforgia, Manuela Capozza, Lucrezia De Cosmo, Antonio Di Mauro, Maria Elisabetta Baldassarre, Francesca Mercadante, Anna Laura Torella, Vincenzo Nigro, Nicoletta Resta

“…Case Reports in Genetics…”
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Tıp fakültesi araştırma görevlilerinde tükenmişlik sendromu ve ilişkili faktörlerin değerlendirilmesi by Mustafa Armutlukuyu, Nisa Çetin Kargın, Kamile Marakoğlu

“…Genel Tıp Dergisi…”
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Identification and Characterization of the Diverse Stress-Responsive R2R3-RMYB Transcription Factor from Hibiscus sabdariffa L. by Bahaeldeen Babikar Mohamed, Beenish Aftab, Muhammad Bilal Sarwar, Bushra Rashid, Zarnab Ahmad, Sameera Hassan, Tayyab Husnain

“…International Journal of Genomics…”
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Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis by Kang Yi, Shao-E He, Tao Guo, Zi-Qiang Wang, Xin Zhang, Jian-Guo Xu, Hao-Yue Zhang, Wei-Guo Liu, Tao You

“…BMC Medical Genomics…”
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QTL Mapping of Traits Associated with Dual Resistance to the African Stem Borer (Busseola fusca) and Spotted Stem Borer (Chilo partellus) in Sorghum (Sorghum bicolor) by Phyllis W. Muturi, Mary Mgonja, Patrick Rubaihayo, James K. Mwololo

“…International Journal of Genomics…”
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Sol internal torasik arterin proksimalinden çıkan gelişmiş aksesuar yan dal ve klinik önemi by Veli Çağlar, Şeref Alpsoy, Dursun Çayan Akkoyun, Aydın Akyüz, Ramazan Uygur

“…Genel Tıp Dergisi…”
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Mask-Related Headache Among Health Workers During COVID-19 Pandemics: Study from Somalia by Mehmet Ufuk Aluçlu, Nor Osman Sidow, Ahmed Muhammad Bashir, Mohamed Sheikh Hassan, Yavuz Yücel

“…Genel Tıp Dergisi…”
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Brain network alterations in anorexia Nervosa: A Multi-Center structural connectivity study by Jun Kanzawa, Ryo Kurokawa, Tsunehiko Takamura, Nobuhiro Nohara, Kouhei Kamiya, Yoshiya Moriguchi, Yasuhiro Sato, Yumi Hamamoto, Tomotaka Shoji, Tomohiko Muratsubaki, Motoaki Sugiura, Shin Fukudo, Yoshiyuki Hirano, Yusuke Sudo, Rio Kamashita, Sayo Hamatani, Noriko Numata, Koji Matsumoto, Eiji Shimizu, Naoki Kodama, Shingo Kakeda, Masatoshi Takahashi, Satoru Ide, Kazumasa Okada, Shu Takakura, Motoharu Gondo, Kazufumi Yoshihara, Masanori Isobe, Keima Tose, Tomomi Noda, Ryo Mishima, Michiko Kawabata, Shun’ichi Noma, Toshiya Murai, Kazuhiro Yoshiuchi, Atsushi Sekiguchi, Osamu Abe

“…NeuroImage: Clinical…”
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A variant W chromosome in Centromochlus heckelii (Siluriformes, Auchenipteridae) and the role of repeated DNA in its heteromorphism by Chrystian Aparecido Grillo Haerter, Patrik Ferreira Viana, Fábio Hiroshi Takagui, Sandro Tonello, Vladimir Pavan Margarido, Daniel Rodrigues Blanco, Josiane Baccarin Traldi, Roberto Laridondo Lui, Eliana Feldberg

“…Genetics and Molecular Biology…”
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PRETRATAMIENTO EN DOS ETAPAS DEL BAGAZO DE CAÑA PARA LA PRODUCCIÓN DE ETANOL A PARTIR DE XILOSA Y GLUCOSA by Leyanis Mesa Garriga, Erenio González Suárez, Yailet Albernas Carvajal

“…Revista Centro Azúcar…”
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Genome-Wide Expression Profiles of Hemp (Cannabis sativa L.) in Response to Drought Stress by Chunsheng Gao, Chaohua Cheng, Lining Zhao, Yongting Yu, Qing Tang, Pengfei Xin, Touming Liu, Zhun Yan, Yuan Guo, Gonggu Zang

“…International Journal of Genomics…”
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Characteristic craniofacial defects associated with a novel USP9X truncation mutation by Namiki Nagata, Hiroshi Kurosaka, Kotaro Higashi, Masaya Yamaguchi, Sayuri Yamamoto, Toshihiro Inubushi, Miho Nagata, Yasuki Ishihara, Ayumi Yonei, Yohei Miyashita, Yoshihiro Asano, Norio Sakai, Yasushi Sakata, Shigetada Kawabata, Takashi Yamashiro

“…Human Genome Variation…”
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Mapping of Novel QTL Regulating Grain Shattering Using Doubled Haploid Population in Rice (Oryza sativa L.) by Gyu-Ho Lee, In-Kyu Kang, Kyung-Min Kim

“…International Journal of Genomics…”
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Hsa_circ_0003220 Drives Chemoresistance of Human NSCLC Cells by Modulating miR-489-3p/IGF1 by Shaofeng Xia, Chenliang Wang

“…International Journal of Genomics…”
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Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome by Tanjung A. Sumekar, Aneel A. Ashrani, Tri I. Winarni, Randi J. Hagerman

“…Case Reports in Genetics…”
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Identification and Expression Analysis of Sugar Transporter Gene Family in Aspergillus oryzae by Gongbo Lv, Chunmiao Jiang, Tiantian Liang, Yayi Tu, Xiaojie Cheng, Bin Zeng, Bin He

“…International Journal of Genomics…”
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Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations by Nirmala D. Sirisena, U. Kalpani S. Wijetunge, Ramya de Silva, Vajira H. W. Dissanayake

“…Case Reports in Genetics…”
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Novel frameshift variant of WNT10A in a Japanese patient with hypodontia by Michiyo Ando, Yoshihiko Aoki, Yasuto Sano, Junya Adachi, Masatoshi Sana, Satoru Miyabe, Satoshi Watanabe, Shogo Hasegawa, Hitoshi Miyachi, Junichiro Machida, Mitsuo Goto, Yoshihito Tokita

“…Human Genome Variation…”
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Laparoskopik kolesistektomide karbondioksit pnömoperitoneumun beyin natriüretik peptid ve troponin I üzerine etkileri by Sevil Kurban, Hande Köksal

“…Genel Tıp Dergisi…”
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Novel Phenotype in Unbalanced 7;9 Translocation with Critical Incidental Finding by Julie Fischer, Luis Rohena

“…Case Reports in Genetics…”
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