Sclerostin Immunoreactivity Increases in Cortical Bone Osteocytes and Decreases in Articular Cartilage Chondrocytes in Aging Mice

door Thompson, Michelle L., Jimenez-Andrade, Juan Miguel, Mantyh, Patrick W.
Gepubliceerd in J Histochem Cytochem (2015)

Solar Radiation during Rewarming from Torpor in Elephant Shrews: Supplementation or Substitution of Endogenous Heat Production?

door Thompson, Michelle L., Mzilikazi, Nomakwezi, Bennett, Nigel C., McKechnie, Andrew E.
Gepubliceerd in PLoS One (2015)

Preventing painful age-related bone fractures: Anti-sclerostin therapy builds cortical bone and increases the proliferation of osteogenic cells in the periosteum of the geriatric m...

door Thompson, Michelle L, Chartier, Stephane R, Mitchell, Stefanie A, Mantyh, Patrick W
Gepubliceerd in Mol Pain (2016)

Exuberant sprouting of sensory and sympathetic nerve fibers in nonhealed bone fractures and the generation and maintenance of chronic skeletal pain

door Chartier, Stephane R., Thompson, Michelle L., Longo, Geraldine, Fealk, Michelle N., Majuta, Lisa A., Mantyh, Patrick W.
Gepubliceerd in Pain (2014)

NGF blockade at early times during bone cancer development attenuates bone destruction and increases limb use

door McCaffrey, Gwen, Thompson, Michelle L., Majuta, Lisa, Fealk, Michelle N., Chartier, Stephane, Longo, Geraldine, Mantyh, Patrick W.
Gepubliceerd in Cancer Res (2014)

Somatic cell selection for chlorsulfuron-resistant mutants in potato: identification of point mutations in the acetohydroxyacid synthase gene

door Barrell, Philippa J., Latimer, Julie M., Baldwin, Samantha J., Thompson, Michelle L., Jacobs, Jeanne M.E., Conner, Anthony J.
Gepubliceerd in BMC Biotechnol (2017)

TorsinA rescues ER-associated stress and locomotive defects in C. elegans models of ALS

door Thompson, Michelle L., Chen, Pan, Yan, Xiaohui, Kim, Hanna, Borom, Akeem R., Roberts, Nathan B., Caldwell, Kim A., Caldwell, Guy A.
Gepubliceerd in 2014

Targeting cells of the myeloid lineage attenuates pain and disease progression in a prostate model of bone cancer

door Thompson, Michelle L., Jimenez-Andrade, Juan Miguel, Chartier, Stephane, Tsai, James, Burton, Elizabeth A., Habets, Gaston, Lin, Paul S., West, Brian L., Mantyh, Patrick W.
Gepubliceerd in Pain (2015)

Yeast reveal a “druggable” Rsp5/Nedd4 Network that Ameliorates α–Synuclein Toxicity in Neurons

door Tardiff, Daniel F., Jui, Nathan T., Khurana, Vikram, Tambe, Mitali A., Thompson, Michelle L., Chung, Chee Yeun, Kamadurai, Hari B., Kim, Hyoung Tae, Lancaster, Alex K., Caldwell, Kim A., Caldwell, Guy A., Rochet, Jean-Christophe, Buchwald, Stephen L., Lindquist, Susan
Gepubliceerd in 2013

MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus

door Blanchet, Patricia, Bebin, Martina, Bruet, Shaam, Cooper, Gregory M., Thompson, Michelle L., Duban-Bedu, Benedicte, Gerard, Benedicte, Piton, Amelie, Suckno, Sylvie, Deshpande, Charu, Clowes, Virginia, Vogt, Julie, Turnpenny, Peter, Williamson, Michael P., Alembik, Yves, Glasgow, Eric, McNeill, Alisdair
Gepubliceerd in PLoS Genet (2017)

Non-coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases

door Cochran, J. Nicholas, Geier, Ethan G., Bonham, Luke W., Newberry, J. Scott, Amaral, Michelle D., Thompson, Michelle L., Lasseigne, Brittany N., Karydas, Anna M., Roberson, Erik D., Cooper, Gregory M., Rabinovici, Gil D., Miller, Bruce L., Myers, Richard M., Yokoyama, Jennifer S.
Gepubliceerd in Am J Hum Genet (2020)

De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy

door Guella, Ilaria, Huh, Linda, McKenzie, Marna B., Toyota, Eric B., Bebin, E. Martina, Thompson, Michelle L., Cooper, Gregory M., Evans, Daniel M., Buerki, Sarah E., Adam, Shelin, Van Allen, Margot I., Nelson, Tanya N., Connolly, Mary B., Farrer, Matthew J., Demos, Michelle
Gepubliceerd in Neurol Genet (2016)

Deleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder

door Hiatt, Susan M., Thompson, Michelle L., Prokop, Jeremy W., Lawlor, James M.J., Gray, David E., Bebin, E. Martina, Rinne, Tuula, Kempers, Marlies, Pfundt, Rolph, van Bon, Bregje W., Mignot, Cyril, Nava, Caroline, Depienne, Christel, Kalsner, Louisa, Rauch, Anita, Joset, Pascal, Bachmann-Gagescu, Ruxandra, Wentzensen, Ingrid M., McWalter, Kirsty, Cooper, Gregory M.
Gepubliceerd in Am J Hum Genet (2019)

Variants in MED12L, encoding a subunit of the Mediator kinase module, are responsible for intellectual disability associated with transcriptional defect

door Nizon, Mathilde, Laugel, Vincent, Flanigan, Kevin M., Pastore, Matthew, Waldrop, Megan A., Rosenfeld, Jill A., Marom, Ronit, Xiao, Rui, Gerard, Amanda, Pichon, Olivier, Caignec, Cédric Le, Gérard, Marion, Dieterich, Klaus, Cho, Megan Truitt, McWalter, Kirsty, Hiatt, Susan, Thompson, Michelle L., Bézieau, Stéphane, Wadley, Alexandrea, Wierenga, Klaas J., Egly, Jean-Marc, Isidor, Bertrand
Gepubliceerd in Genet Med (2019)

Genomic sequencing identifies secondary findings in a cohort of parent study participants

door Thompson, Michelle L., Finnila, Candice R., Bowling, Kevin M., Brothers, Kyle B., Neu, Matthew B., Amaral, Michelle D., Hiatt, Susan M., East, Kelly M., Gray, David E., Lawlor, James M.J., Kelley, Whitley V., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Levy, Shawn E., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Gepubliceerd in Genet Med (2018)

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

door Cochran, J. Nicholas, McKinley, Emily C., Cochran, Meagan, Amaral, Michelle D., Moyers, Bryan A., Lasseigne, Brittany N., Gray, David E., Lawlor, James M.J., Prokop, Jeremy W., Geier, Ethan G., Holt, James M., Thompson, Michelle L., Newberry, J. Scott, Yokoyama, Jennifer S., Worthey, Elizabeth A., Geldmacher, David S., Love, Marissa Natelson, Cooper, Gregory M., Myers, Richard M., Roberson, Erik D.
Gepubliceerd in Cold Spring Harb Mol Case Stud (2019)

A State-Based Approach to Genomics for Rare Disease and Population Screening

door East, Kelly M., Kelley, Whitley V., Cannon, Ashley, Cochran, Meagan E., Moss, Irene P., May, Thomas, Nakano-Okuno, Mariko, Sodeke, Stephen O., Edberg, Jeffrey C., Cimino, James J., Fouad, Mona, Curry, William A., Hurst, Anna C.E., Bowling, Kevin M., Thompson, Michelle L., Bebin, E. Martina, Johnson, Robert D., Cooper, Gregory M., Might, Matthew, Barsh, Gregory S., Korf, Bruce R.
Gepubliceerd in Genet Med (2020)

Genomic diagnosis for children with intellectual disability and/or developmental delay

door Bowling, Kevin M., Thompson, Michelle L., Amaral, Michelle D., Finnila, Candice R., Hiatt, Susan M., Engel, Krysta L., Cochran, J. Nicholas, Brothers, Kyle B., East, Kelly M., Gray, David E., Kelley, Whitley V., Lamb, Neil E., Lose, Edward J., Rich, Carla A., Simmons, Shirley, Whittle, Jana S., Weaver, Benjamin T., Nesmith, Amy S., Myers, Richard M., Barsh, Gregory S., Bebin, E. Martina, Cooper, Gregory M.
Gepubliceerd in Genome Med (2017)

Systematic reanalysis of genomic data improves quality of variant interpretation

door Hiatt, Susan M., Amaral, Michelle D., Bowling, Kevin M., Finnila, Candice R., Thompson, Michelle L., Gray, David E., Lawlor, James M.J., Cochran, J. Nicholas, Bebin, E. Martina, Brothers, Kyle B., East, Kelly M., Kelley, Whitley V., Lamb, Neil E., Levy, Shawn E., Lose, Edward J., Neu, Matthew B., Rich, Carla A., Simmons, Shirley, Myers, Richard M., Barsh, Gregory S., Cooper, Gregory M.
Gepubliceerd in Clin Genet (2018)

Defining the phenotype of FHF1 developmental and epileptic encephalopathy

door Trivisano, Marina, Ferretti, Alessandro, Bebin, Elizabeth, Huh, Linda, Lesca, Gaetan, Siekierska, Aleksandra, Takeguchi, Ryo, Carneiro, Maryline, De Palma, Luca, Guella, Ilaria, Haginoya, Kazuhiro, Shi, Ruo Ming, Kikuchi, Atsuo, Kobayashi, Tomoko, Jung, Julien, Lagae, Lieven, Milh, Mathieu, Mathieu, Marie L, Minassian, Berge A, Novelli, Antonio, Pietrafusa, Nicola, Takeshita, Eri, Tartaglia, Marco, Terracciano, Alessandra, Thompson, Michelle L, Cooper, Gregory M, Vigevano, Federico, Villard, Laurent, Villeneuve, Nathalie, Buyse, Gunnar M, Demos, Michelle, Scheffer, Ingrid E, Specchio, Nicola
Gepubliceerd in Epilepsia (2020)