Guoling Tian

Guoling Tian, PhD

Research Assistant Professor, Department of Neuroscience and Physiology

Positions

Research Assistant Professor, Department of Neuroscience and Physiology at NYU Grossman School of Medicine

Graduate Education

PhD from New York University School of Medicine

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Functional specialization of hippocampal somatostatin-expressing interneurons

Chamberland, Simon; Grant, Gariel; Machold, Robert; Nebet, Erica R; Tian, Guoling; Stich, Joshua; Hanani, Monica; Kullander, Klas; Tsien, Richard W

Proceedings of the National Academy of Sciences of the United States of America (PNAS). 2024 Apr 23; 121(17):e2306382121

Synaptic homeostasis transiently leverages Hebbian mechanisms for a multiphasic response to inactivity

Sun, Simón E D; Levenstein, Daniel; Li, Boxing; Mandelberg, Nataniel; Chenouard, Nicolas; Suutari, Benjamin S; Sanchez, Sandrine; Tian, Guoling; Rinzel, John; Buzsáki, György; Tsien, Richard W

Cell reports. 2024 Mar 19; 43(4):113839

Functional specialization of hippocampal somatostatin-expressing interneurons

Chamberland, Simon; Grant, Gariel; Machold, Robert; Nebet, Erica R; Tian, Guoling; Hanani, Monica; Kullander, Klas; Tsien, Richard W

bioRxiv.org : the preprint server for biology. 2023 Apr 27;

Neuronal Inactivity Co-opts LTP Machinery to Drive Potassium Channel Splicing and Homeostatic Spike Widening

Li, Boxing; Suutari, Benjamin S; Sun, Simon D; Luo, Zhengyi; Wei, Chuanchuan; Chenouard, Nicolas; Mandelberg, Natanial J; Zhang, Guoan; Wamsley, Brie; Tian, Guoling; Sanchez, Sandrine; You, Sikun; Huang, Lianyan; Neubert, Thomas A; Fishell, Gordon; Tsien, Richard W

Cell. 2020 Jun 25; 181(7):1547-1565.e15

Mutations in MAST1 Cause Mega-Corpus-Callosum Syndrome with Cerebellar Hypoplasia and Cortical Malformations

Tripathy, Ratna; Leca, Ines; van Dijk, Tessa; Weiss, Janneke; van Bon, Bregje W; Sergaki, Maria Christina; Gstrein, Thomas; Breuss, Martin; Tian, Guoling; Bahi-Buisson, Nadia; Paciorkowski, Alexander R; Pagnamenta, Alistair T; Wenninger-Weinzierl, Andrea; Martinez-Reza, Maria Fernanda; Landler, Lukas; Lise, Stefano; Taylor, Jenny C; Terrone, Gaetano; Vitiello, Giuseppina; Del Giudice, Ennio; Brunetti-Pierri, Nicola; D'Amico, Alessandra; Reymond, Alexandre; Voisin, Norine; Bernstein, Jonathan A; Farrelly, Ellyn; Kini, Usha; Leonard, Thomas A; Valence, Stéphanie; Burglen, Lydie; Armstrong, Linlea; Hiatt, Susan M; Cooper, Gregory M; Aldinger, Kimberly A; Dobyns, William B; Mirzaa, Ghayda; Pierson, Tyler Mark; Baas, Frank; Chelly, Jamel; Cowan, Nicholas J; Keays, David Anthony

Neuron. 2018 Dec 19; 100(6):1354-1368.e5

Mutations in TUBB4B Cause a Distinctive Sensorineural Disease

Luscan, Romain; Mechaussier, Sabrina; Paul, Antoine; Tian, Guoling; Gérard, Xavier; Defoort-Dellhemmes, Sabine; Loundon, Natalie; Audo, Isabelle; Bonnin, Sophie; LeGargasson, Jean-François; Dumont, Julien; Goudin, Nicolas; Garfa-Traoré, Meriem; Bras, Marc; Pouliet, Aurore; Bessières, Bettina; Boddaert, Nathalie; Sahel, José-Alain; Lyonnet, Stanislas; Kaplan, Josseline; Cowan, Nicholas J; Rozet, Jean-Michel; Marlin, Sandrine; Perrault, Isabelle

American journal of human genetics. 2017 Dec 07; 101(6):1006-1012

Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability

Breuss, Martin W; Nguyen, Thai; Srivatsan, Anjana; Leca, Ines; Tian, Guoling; Fritz, Tanja; Hansen, Andi H; Musaev, Damir; McEvoy-Venneri, Jennifer; James, Kiely N; Rosti, Rasim O; Scott, Eric; Tan, Uner; Kolodner, Richard D; Cowan, Nicholas J; Keays, David A; Gleeson, Joseph G

Human molecular genetics. 2017 01 15; 26(2):258-269

Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathway

Edvardson, Shimon; Tian, Guoling; Cullen, Hayley; Vanyai, Hannah; Ngo, Linh; Bhat, Saiuj; Aran, Adi; Daana, Muhannad; Da'amseh, Naderah; Abu-Libdeh, Bassam; Cowan, Nicholas J; Heng, Julian Ik-Tsen; Elpeleg, Orly

Human molecular genetics. 2016 11 01; 25(21):4635-4648

See All Publications (35)