日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Chromosome level genome and full length transcriptome of long whiskers catfish, Mystus gulio (Hamilton, 1822)

长须鲶(Mystus gulio (Hamilton, 1822))的染色体水平基因组和全长转录组

Prabhudas, Sudheesh K; Katneni, Vinaya Kumar; Jangam, Ashok Kumar; Krishnan, Karthic; Selvaraj, Ashok; Angel, Jesudhas Raymond Jani; Shekhar, Mudagandur S

Resolving SLC6A1 variable expressivity with deep clinical phenotyping and Drosophila models

利用深度临床表型分析和果蝇模型解析SLC6A1基因表达变异性

Jay, Kristy L; Gogate, Nikhita; Hall, Paige I; Ezell, Kimberly M; Andrews, Jonathan C; Jangam, Sharayu V; Pan, Hongling; Pham, Kelvin; German, Ryan; Gomez, Vanessa; Jellinek-Russo, Emily; Storch, Eric A; Yamamoto, Shinya; Kanca, Oguz; Bellen, Hugo J; Dierick, Herman A; Cogan, Joy D; Phillips, John A; Hamid, Rizwan; Cassini, Thomas; Rives, Lynette; Pruthi, Sumit; Chen, Hua-Chang; Posey, Jennifer E; Wangler, Michael F

Short dual antiplatelet therapy after PCI with Resolute Onyx drug-eluting stents in high bleeding risk patients: One-year outcomes from a South Asian cohort

高出血风险患者经皮冠状动脉介入治疗(PCI)植入Resolute Onyx药物洗脱支架后短期双联抗血小板治疗:来自南亚队列的一年结果

Jariwala, Pankaj; Vallapuri, Guna Sai; Konda, Bharat Kumar Reddy; Jangam, Sukesh Kumar

NLGN3 autism variants have distinct functional impact on synapses and sleep behavior in Drosophila

NLGN3自闭症变异体对果蝇的突触和睡眠行为具有不同的功能影响

Townsley, Rebekah E; Andrews, Jonathan C; Srivastav, Saurabh; Jangam, Sharayu V; Hannan, Shabab B; Kanca, Oguz; Yamamoto, Shinya; Wangler, Michael F

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome

DDX39B基因的新生突变和遗传突变会导致一种新的神经发育综合征。

Booth, Kevin T A; Jangam, Sharayu V; Chui, Martin M C; Treat, Kayla; Graziani, Lorenzo; Soldano, Alessia; Ruan, Yao; Wan-Hei Hui, Jeffrey; White, Kerry; Christensen, Celanie K; Lynnes, Ty; Yamamoto, Shinya; Kanca, Oguz; Tsang, Mandy H Y; Lynch, Sally A; Mullegama, Sureni V; Baptista, Julia; Iancu, Daniela; Joss, Shelagh K; Wong, Sandra Y Y; Mak, Christopher C Y; Kwong, Anna K Y; Bellen, Hugo J; Conboy, Erin; Sanges, Remo; Leung, Anskar Yu-Hung; Wangler, Michael F; Chung, Brian H Y; Vetrini, Francesco

Chromosome-level genome assembly with telomeric repeats at scaffold ends for Rhabdosargus sarba

利用端粒重复序列对沙棘鱼(Rhabdosargus sarba)进行染色体水平基因组组装,支架末端包含端粒重复序列。

Shekhar, Mudagandur S; Katneni, Vinaya Kumar; Jangam, Ashok Kumar; Krishnan, Karthic; Prabhudas, Sudheesh K; Raymond, Jesudhas Jani Angel; Lal, Kuldeep K

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

RYBP基因的新生突变与严重的神经发育障碍和先天性异常有关。

Weisz-Hubshman, Monika; Burrage, Lindsay C; Jangam, Sharayu V; Rosenfeld, Jill A; von Hardenberg, Sandra; Bergmann, Anke; Richter, Manuela Friederike; Rydzanicz, Malgorzata; Ploski, Rafal; Stembalska, Agnieszka; Chung, Wendy K; Hernan, Rebecca R; Lim, Foong Y; Brunet, Theresa; Syrbe, Steffen; Keren, Boris; Heide, Solveig; Murdock, David R; Dai, Hongzheng; Xia, Fan; Ketkar, Shamika; Dawson, Brian; Narayanan, Vinodh; Graves, Hillary K; Wangler, Michael F; Bacino, Carlos; Lee, Brendan

Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders.

区分 PEX2 和 PEX16 基因变异对轻度、重度和非典型过氧化物酶体生物合成障碍的严重程度

Gomez Vanessa A, Kanca Oguz, Jangam Sharayu V, Srivastav Saurabh, Andrews Jonathan C, Wangler Michael F

Gender and personal safety sensitization in schools: A qualitative inquiry into response practices to children's disclosures of sexual abuse

学校中的性别与人身安全意识教育:对儿童披露性虐待事件的应对措施的定性研究

Ramakrishna, Sathish K; Sharma, Eesha; Jangam, Kavitha V; Rajendra, K M

Psychosocial Perspectives on Child Mental Health in Custody Disputes: A Qualitative Study from India

印度监护权纠纷中儿童心理健康的社会心理视角:一项定性研究

Nambiar, Priyanka P; Jangam, Kavita V; Seshadri, Shekhar P