logo
CanyamAI summaries for academic research
language
MobileMobile
  • Phone FeatureWeChat Mini Program
EnglishEnglish
noticeNotice
BlogBlog
delete
arrow
Back
H

Hugo J. Bellen

Indiana University Bloomington

117H-index
611Paper Count
4.8WCitation Count
Published Papers 207
Publication Date
logo
Aberrant nuclear pore complex degradation contributes to neurodegeneration in VCP disease
errNeuron
IF15
err2025-12-30
err0
PREAI
errSandeep Kumar Dubey; Divya Chaubey; Chiseko Ikenaga; Wen-Wen Lin; Hugo J. Bellen; Thomas E. Lloyd
errShare
errSave
Resolving SLC6A1 variable expressivity with deep clinical phenotyping and Drosophila models
errHuman Genetics and Genomics Advances
IF3.6
err2025-10-31
err0
errOAAI
errKristy L. Jay; Nikhita Gogate; Paige I. Hall; Kimberly M. Ezell; Jonathan C. Andrews; Sharayu V. Jangam; Hongling Pan; Kelvin Pham; Ryan German; Vanessa Gomez; Emily Jellinek-Russo; Eric Storch; Shinya Yamamoto; Oguz Kanca; Hugo J. Bellen; Herman Dierick; Joy D. Cogan; John A. Phillips; Rizwan Hamid; Thomas Cassini; Lynette Rives; Sumit Pruthi; Hua-Chang Chen; Jennifer E. Posey; Michael F. Wangler
errShare
errSave
Revealing the nervous system requirements of Alzheimer disease risk genes in Drosophila
errThe American Journal of Human Genetics
IF0
err2025-10-29
err0
errOAAI
errJennifer M. Deger; Shabab B. Hannan; Mingxue Gu; Colleen E. Strohlein; Lindsey D. Goodman; Sasidhar Pasupuleti; Zahid Shaik; Liwen Ma; Yarong Li; Jiayang Li; Morgan C. Stephens; Michal Tyrlík; Zhandong Liu; Ismael Al-Ramahi; Juan Botas; Chad A. Shaw; Oguz Kanca; Hugo J. Bellen; Joshua M. Shulman
errShare
errSave
APOA1 binding protein promotes lymphatic cell fate and lymphangiogenesis by relieving caveolae-mediated inhibition of VEGFR3 signaling
errNature Communications
IF15.7
err2025-10-21
err0
errOAAI
errJun-dae Kim; Surbhi Chaudhary; Weiqing Chen; Jonathan Astin; Philip S. Crosier; Pengchun Yu; John P. Cooke; Henry J. Pownall; Hugo J. Bellen; Nhat-Tu Le; Daniel L. Kiss; Guangyu Wang; Stanley G. Rockson; Hong Chen; Longhou Fang
errShare
errSave
Alzheimer's disease protective allele of Clusterin modulates neuronal excitability through lipid-droplet-mediated neuron-glia communication
errMOLECULAR NEURODEGENERATION
IF17.5
err2025-05-03
err0
errOAAI
errZhao, Xiaojie; Li, Yan; Zhang, Siwei; Sudwarts, Ari; Zhang, Hanwen; Kozlova, Alena; Moulton, Matthew J.; Goodman, Lindsey D.; Pang, Zhiping P.; Sanders, Alan R.; Bellen, Hugo J.; Thinakaran, Gopal; Duan, Jubao
errShare
errSave
De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome
errBRAIN
IF11.7
err2025-05-01
err3
PREAI
errBooth, Kevin T. A.; Jangam, Sharayu, V; Chui, Martin M. C.; Treat, Kayla; Graziani, Lorenzo; Soldano, Alessia; Ruan, Yao; Hui, Jeffrey Wan-Hei; 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
errShare
errSave
De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-04-01
err0
PREAI
errBereshneh, Ali H.; Andrews, Jonathan C.; Eberl, Daniel F.; Bademci, Guney; Borja, Nicholas A.; Bivona, Stephanie; Chung, Wendy K.; Yamamoto, Shinya; Wangler, Michael F.; McKee, Shane; Tekin, Mustafa; Bellen, Hugo J.; Kanca, Oguz
errShare
errSave
A neuroprotective role of polyunsaturated fatty acids in C9orf72-ALS/FTD
errNATURE NEUROSCIENCE
IF20
err2025-03-26
err0
PREAI
errDubey, Sandeep Kumar; Bellen, Hugo J.
errShare
errSave
Does glial lipid dysregulation alter sleep in Alzheimer's ' s and Parkinson's ' s disease?
errTrends in Molecular Medicine
IF13.8
err2024-10-01
err1
PREAI
errGoodman, Lindsey D.; Moulton, Matthew J.; Lin, Guang; Bellen, Hugo J.
errShare
errSave
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma
errGENETICS IN MEDICINE
IF6.2
err2024-07-01
err0
PREAI
errMa, Mengqi; Ganapathi, Mythily; Zheng, Yiming; Tan, Kai-Li; Kanca, Oguz; Bove, Kevin E.; Quintanilla, Norma; Sag, Sebnem O.; Temel, Sehime G.; LeDuc, Charles A.; McPartland, Amanda J.; Pereira, Elaine M.; Shen, Yufeng; Hagen, Jacob; Thomas, Christie P.; Galvan, Nhu Thao Nguyen; Pan, Xueyang; Lu, Shenzhao; Rosenfeld, Jill A.; Calame, Daniel G.; Wangler, Michael F.; Lupski, James R.; Pehlivan, Davut; Hertel, Paula M.; Chung, Wendy K.; Bellen, Hugo J.
errShare
errSave
Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila
errNATURE COMMUNICATIONS
IF15.7
err2024-04-18
err0
errOAAI
errLiao, Jenny Zhe; Chung, Hyung-lok; Shih, Claire; Wong, Kenneth Kin Lam; Dutta, Debdeep; Nil, Zelha; Burns, Catherine Grace; Kanca, Oguz; Park, Ye-Jin; Zuo, Zhongyuan; Marcogliese, Paul C.; Sew, Katherine; Bellen, Hugo J.; Verheyen, Esther M.
errShare
errSave
Identifying potential dietary treatments for inherited metabolic disorders using Drosophila nutrigenomics
errCELL REPORTS
IF6.9
err2024-03-01
err2
errOAAI
errMartelli, Felipe; Lin, Jiayi; Mele, Sarah; Imlach, Wendy; Kanca, Oguz; Barlow, Christopher K.; Paril, Jefferson; Schittenhelm, Ralf B.; Christodoulou, John; Bellen, Hugo J.; Piper, Matthew D. W.; Johnson, Travis K.
errShare
errSave
OXR1 maintains the retromer to delay brain aging under dietary restriction
errNATURE COMMUNICATIONS
IF15.7
err2024-01-11
err1
errOAAI
errWilson, Kenneth A.; Bar, Sudipta; Dammer, Eric B.; Carrera, Enrique M.; Hodge, Brian A.; Hilsabeck, Tyler A. U.; Bons, Joanna; Brownridge, George W.; Beck, Jennifer N.; Rose, Jacob; Granath-Panelo, Melia; Nelson, Christopher S.; Qi, Grace; Gerencser, Akos A.; Lan, Jianfeng; Afenjar, Alexandra; Chawla, Geetanjali; Brem, Rachel B.; Campeau, Philippe M.; Bellen, Hugo J.; Schilling, Birgit; Seyfried, Nicholas T.; Ellerby, Lisa M.; Kapahi, Pankaj
errShare
errSave
Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays
errELIFE
IF0
err2023-12-11
err1
errOAAI
errPan, Xueyang; Alvarez, Albert N.; Ma, Mengqi; Lu, Shenzhao; Crawford, Michael W.; Briere, Lauren C.; Kanca, Oguz; Yamamoto, Shinya; Sweetser, David A.; Wilson, Jenny L.; Napier, Ruth J.; Pruneda, Jonathan N.; Bellen, Hugo J.
errShare
errSave
Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2023-11-01
err2
errOAAI
errNil, Zelha; Deshwar, Ashish R.; Huang, Yan; Barish, Scott; Zhang, Xi; Choufani, Sanaa; Stabej, Polona Le Quesne; Hayes, Ian; Yap, Patrick; Haldeman-Englert, Chad; Wilson, Carolyn; Prescott, Trine; Tveten, Kristian; Vollo, Arve; Haynes, Devon; Wheeler, Patricia G.; Zon, Jessica; Cytrynbaum, Cheryl; Jobling, Rebekah; Blyth, Moira; Banka, Siddharth; Afenjar, Alexandra; Mignot, Cyril; Robin-Renaldo, Florence; Keren, Boris; Kanca, Oguz; Mao, Xiao; Wegner, Daniel J.; Sisco, Kathleen; Shinawi, Marwan; Wangler, Michael F.; Weksberg, Rosanna; Yamamoto, Shinya; Costain, Gregory; Bellen, Hugo J.
errShare
errSave
A defect in mitochondrial fatty acid synthesis impairs iron metabolism and causes elevated ceramide levels
errNATURE METABOLISM
IF20.8
err2023-08-31
err5
errOAAI
errDutta, Debdeep; Kanca, Oguz; Byeon, Seul Kee; Marcogliese, Paul C.; Zuo, Zhongyuan; Shridharan, Rishi V.; Park, Jun Hyoung; Undiagnosed Dis Network, Guang; Lin, Guang; Ge, Ming; Heimer, Gali; Kohler, Jennefer N.; Wheeler, Matthew T.; Kaipparettu, Benny A.; Pandey, Akhilesh; Bellen, Hugo J.
errShare
errSave
Daam2 phosphorylation by CK2α negatively regulates Wnt activity during white matter development and injury
errPROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
IF9.1
err2023-08-22
err0
errOAAI
errWang, Chih-Yen; Zuo, Zhongyuan; Jo, Juyeon; Kim, Kyoung In; Madamba, Christine; Ye, Qi; Jung, Sung Yun; Bellen, Hugo J.; Lee, Hyun Kyoung
errShare
errSave
Highlighting rare disease research with a GENETICS and G3 series on genetic models of rare diseases
errGENETICS
IF5.1
err2023-08-09
err0
errOAAI
errHieter, Philip; Andrews, Brenda; Fowler, Douglas; Bellen, Hugo
errShare
errSave
Integrating non-mammalian model organisms in the diagnosis of rare genetic diseases in humans
errNATURE REVIEWS GENETICS
IF52
err2023-07-25
err28
PREAI
errYamamoto, Shinya; Kanca, Oguz; Wangler, Michael F.; Bellen, Hugo J.
errShare
errSave
Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation
errCELL METABOLISM
IF30.9
err2023-05-01
err22
errOAAI
errChung, Hyung-lok; Ye, Qi; Park, Ye-Jin; Zuo, Zhongyuan; Mok, Jung-Wan; Kanca, Oguz; Tattikota, Sudhir Gopal; Lu, Shenzhao; Perrimon, Norbert; Lee, Hyun Kyoung; Bellen, Hugo J.
errShare
errSave

Research Directions

No research directions
Co-authors
Cooperation Journals
C
Cornelia M. van Duijn
H-index: 238 · Papers: 1.9K
A
André G. Uitterlinden
H-index: 234 · Papers: 2.0K
D
Daniel Levy
H-index: 230 · Papers: 1.6K
E
Eric Boerwinkle
H-index: 215 · Papers: 2.0K
M
M Snyder
H-index: 210 · Papers: 3.3K
View more