Determinants of Power in Gene-Based Burden Testing for Monogenic Disorders von Guo, Michael H., Dauber, Andrew, Lippincott, Margaret F., Chan, Yee-Ming, Salem, Rany M., Hirschhorn, Joel N.

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Interrogation of human hematopoiesis at single-cell and single-variant resolution von Ulirsch, Jacob C., Lareau, Caleb A., Bao, Erik L., Ludwig, Leif S., Guo, Michael H., Benner, Christian, Satpathy, Ansuman T., Kartha, Vinay K., Salem, Rany M., Hirschhorn, Joel N., Finucane, Hilary K., Aryee, Martin J., Buenrostro, Jason D., Sankaran, Vijay G.

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Using the time and motion method to study clinical work processes and workflow: methodological inconsistencies and a call for standardized research von Zheng, Kai, Guo, Michael H, Hanauer, David A

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Development of a low back pain care pathway in an academic hospital system: results of a consensus process von Bejarano, Geronimo, Vining, Robert, Desai, Devan P, Minchew, Joe, Michael Guo, H, Goertz, Christine

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Short Stature, Accelerated Bone Maturation, and Early Growth Cessation Due to Heterozygous Aggrecan Mutations von Nilsson, Ola, Guo, Michael H, Dunbar, Nancy, Popovic, Jadranka, Flynn, Daniel, Jacobsen, Christina, Lui, Julian C, Hirschhorn, Joel N, Baron, Jeffrey, Dauber, Andrew

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Genome-wide analysis of body proportion classifies height-associated variants by mechanism of action and implicates genes important for skeletal development von Chan, Yingleong, Salem, Rany M., H Hsu, Yu-Han, McMahon, George, Pers, Tune H., Vedantam, Sailaja, Esko, Tonu, Guo, Michael H., Lim, Elaine T., Franke, Lude, Smith, George Davey, Strachan, David P., Hirschhorn, Joel N.

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TMEM106B Effect on cognition in Parkinson disease and frontotemporal dementia von Tropea, Thomas F., Mak, Jordan, Guo, Michael H., Xie, Sharon X., Suh, Eunran, Rick, Jacqueline, Siderowf, Andrew, Weintraub, Daniel, Grossman, Murray, Irwin, David, Wolk, David A., Trojanowski, John Q., Van Deerlin, Vivianna, Chen‐Plotkin, Alice S.

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Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells von Giani, Felix C., Fiorini, Claudia, Wakabayashi, Aoi, Ludwig, Leif S., Salem, Rany M., Jobaliya, Chintan D., Regan, Stephanie N., Ulirsch, Jacob C., Liang, Ge, Steinberg-Shemer, Orna, Guo, Michael H., Esko, Tõnu, Tong, Wei, Brugnara, Carlo, Hirschhorn, Joel N., Weiss, Mitchell J., Zon, Leonard I., Chou, Stella T., French, Deborah L., Musunuru, Kiran, Sankaran, Vijay G.

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Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets von Guo, Michael H, Sama, Prashanth, LaBarre, Brenna A, Lokhande, Hrishikesh, Balibalos, John, Chu, Ci, Du, Xiaomi, Kheradpour, Pouya, Kim, Charles C, Oniskey, Taylor, Snyder, Thomas, Soghoian, Damien Z, Weiner, Howard L, Chitnis, Tanuja, Patsopoulos, Nikolaos A

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A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development von Cesana, Marcella, Guo, Michael H., Cacchiarelli, Davide, Wahlster, Lara, Barragan, Jessica, Doulatov, Sergei, Vo, Linda T., Salvatori, Beatrice, Trapnell, Cole, Clement, Kendell, Cahan, Patrick, Tsanov, Kaloyan M., Sousa, Patricia M., Tazon-Vega, Barbara, Bolondi, Adriano, Giorgi, Federico M., Califano, Andrea, Rinn, John L., Meissner, Alexander, Hirschhorn, Joel N., Daley, George Q.

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Whole Exome Sequencing to Identify Genetic Causes of Short Stature von Guo, Michael H., Shen, Yiping, Walvoord, Emily C., Miller, Timothy C., Moon, Jennifer E., Hirschhorn, Joel N., Dauber, Andrew

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A 46,XX Ovotesticular Disorder of Sex Development Likely Caused by a Steroidogenic Factor-1 (NR5A1) Variant von Swartz, Jonathan M., Ciarlo, Ryan, Guo, Michael H., Abrha, Aser, Weaver, Benjamin, Diamond, David A., Chan, Yee-Ming, Hirschhorn, Joel N.

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Estimating yields of prenatal carrier screening and implications for design of expanded carrier screening panels von Guo, Michael H., Gregg, Anthony R.

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The Importance of Offering Exome or Genome Sequencing in Adult Neuromuscular Clinics von Dratch, Laynie, Bardakjian, Tanya M, Johnson, Kelsey, Babaian, Nareen, Gonzalez-Alegre, Pedro, Elman, Lauren, Quinn, Colin, Guo, Michael H, Scherer, Steven S, Amado, Defne A

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Osteoimmunology: Interactions With the Immune System in Spinal Fusion von Bergin, Stephen M, Crutcher, Clifford L, Keeler, Carolyn, Rocos, Brett, Haglund, Michael M, Michael Guo, H, Gottfried, Oren N, Richardson, William J, Than, Khoi D

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Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data von Guo, Michael H., Plummer, Lacey, Chan, Yee-Ming, Hirschhorn, Joel N., Lippincott, Margaret F.

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Expanding Genetic and Functional Diagnoses of IGF1R Haploinsufficiencies von Ocaranza, Paula, Golekoh, Marjorie C., Andrew, Shayne F., Guo, Michael H., Kaplowitz, Paul, Saal, Howard, Rosenfeld, Ron G., Dauber, Andrew, Cassorla, Fernando, Backeljauw, Philippe F., Hwa, Vivian

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Insights and implications of genome wide association studies of height von Guo, Michael H, Hirschhorn, Joel N, Dauber, Andrew

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Three-dimensional genome restructuring across timescales of activity-induced neuronal gene expression von Beagan, Jonathan A., Pastuzyn, Elissa D., Fernandez, Lindsey R., Guo, Michael H., Feng, Kelly, Titus, Katelyn R., Chandrashekar, Harshini, Shepherd, Jason D., Phillips-Cremins, Jennifer E.

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The Genetic Landscape of Diamond-Blackfan Anemia von Ulirsch, Jacob C., Verboon, Jeffrey M., Kazerounian, Shideh, Guo, Michael H., Yuan, Daniel, Ludwig, Leif S., Handsaker, Robert E., Abdulhay, Nour J., Fiorini, Claudia, Genovese, Giulio, Lim, Elaine T., Cheng, Aaron, Cummings, Beryl B., Chao, Katherine R., Beggs, Alan H., Genetti, Casie A., Sieff, Colin A., Newburger, Peter E., Niewiadomska, Edyta, Matysiak, Michal, Vlachos, Adrianna, Lipton, Jeffrey M., Atsidaftos, Eva, Glader, Bertil, Narla, Anupama, Gleizes, Pierre-Emmanuel, O’Donohue, Marie-Françoise, Montel-Lehry, Nathalie, Amor, David J., McCarroll, Steven A., O’Donnell-Luria, Anne H., Gupta, Namrata, Gabriel, Stacey B., MacArthur, Daniel G., Lander, Eric S., Lek, Monkol, Da Costa, Lydie, Nathan, David G., Korostelev, Andrei A., Do, Ron, Sankaran, Vijay G., Gazda, Hanna T.

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