Recruitment of Activation Receptors at Inhibitory NK Cell Immune Synapses

por Schleinitz, Nicolas, March, Michael E., Long, Eric O.
Publicado 2008

Genetic polymorphisms and associated susceptibility to asthma

por March, Michael E, Sleiman, Patrick MA, Hakonarson, Hakon
Publicado 2013

Cytolytic granule polarization and degranulation controlled by different receptors in resting NK cells

por Bryceson, Yenan T., March, Michael E., Barber, Domingo F., Ljunggren, Hans-Gustaf, Long, Eric O.
Publicado 2005

The Role of Autophagy in Skeletal Muscle Diseases

por Xia, Qianghua, Huang, Xubo, Huang, Jieru, Zheng, Yongfeng, March, Michael E., Li, Jin, Wei, Yongjie
Publicado 2021

HIF-1α Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions

por Kelchtermans, Jelte, Chang, Xiao, March, Michael E., Mentch, Frank, Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2021

Kaposiform lymphangiomatosis effectively treated with MEK inhibition

por Foster, Jessica B, Li, Dong, March, Michael E, Sheppard, Sarah E, Adams, Denise M, Hakonarson, Hakon, Dori, Yoav
Publicado 2020

Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant

por Desai, Akshatha, Connolly, John J., March, Michael, Hou, Cuiping, Chiavacci, Rosetta, Kim, Cecilia, Lyon, Gholson, Hadley, Dexter, Hakonarson, Hakon
Publicado 2016

Discovery of Novel Host Molecular Factors Underlying HBV/HCV Infection

por Huang, Xubo, Glessner, Joseph T., Huang, Jinxia, Zhou, Desheng, March, Michael E., Wang, Hongna, Xia, Qianghua, Hakonarson, Hakon, Li, Jin
Publicado 2021

Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils

por Li, Junyi, Yuan, Xiucheng, March, Michael E., Yao, Xueming, Sun, Yan, Chang, Xiao, Hakonarson, Hakon, Xia, Qianghua, Meng, Xinyi, Li, Jin
Publicado 2019

Target Genes of Autism Risk Loci in Brain Frontal Cortex

por Sun, Yan, Yao, Xueming, March, Michael E., Meng, Xinyi, Li, Junyi, Wei, Zhi, Sleiman, Patrick M.A., Hakonarson, Hakon, Xia, Qianghua, Li, Jin
Publicado 2019

Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples

por Qu, Hui-Qi, Kao, Charlly, Garifallou, James, Wang, Fengxiang, Snyder, James, Slater, Diana J., Hou, Cuiping, March, Michael, Connolly, John J., Glessner, Joseph T., Hakonarson, Hakon
Publicado 2023

Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients

por Qu, Jingchun, Qu, Hui-Qi, Bradfield, Jonathan P., Glessner, Joseph T., Chang, Xiao, Tian, Lifeng, March, Michael, Connolly, John J., Roizen, Jeffrey D., Sleiman, Patrick M. A., Hakonarson, Hakon
Publicado 2021

Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders

por Glessner, Joseph T., Li, Jin, Wang, Dai, March, Michael, Lima, Leandro, Desai, Akshatha, Hadley, Dexter, Kao, Charlly, Gur, Raquel E., Cohen, Nadine, Sleiman, Patrick M. A., Li, Qingqin, Hakonarson, Hakon
Publicado 2017

Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci

por Qu, Hui-Qi, Qu, Jingchun, Bradfield, Jonathan, Marchand, Luc, Glessner, Joseph, Chang, Xiao, March, Michael, Li, Jin, Connolly, John J., Roizen, Jeffrey D., Sleiman, Patrick, Polychronakos, Constantin, Hakonarson, Hakon
Publicado 2021

Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders

por Yao, Xueming, Glessner, Joseph T., Li, Junyi, Qi, Xiaohui, Hou, Xiaoyuan, Zhu, Chonggui, Li, Xiaoge, March, Michael E., Yang, Liu, Mentch, Frank D., Hain, Heather S., Meng, Xinyi, Xia, Qianghua, Hakonarson, Hakon, Li, Jin
Publicado 2021

Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

por Liu, Yichuan, Li, Yun, March, Michael E., Kenny, Nguyen, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Publicado 2015

Erratum to: Copy number variation in CEP57L1 predisposes to congenital absence of bilateral ACL and PCL ligaments

por Liu, Yichuan, Li, Yun, March, Michael E., Nguyen, Kenny, Xu, Kexiang, Wang, Fengxiang, Guo, Yiran, Keating, Brendan, Glessner, Joseph, Li, Jiankang, Ganley, Theodore J., Zhang, Jianguo, Deardorff, Matthew A., Xu, Xun, Hakonarson, Hakon
Publicado 2016

Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study

por Cardinale, Christopher J., Li, Dong, Tian, Lifeng, Connolly, John J., March, Michael E., Hou, Cuiping, Wang, Fengxiang, Snyder, James, Kim, Cecilia E., Chiavacci, Rosetta M., Sleiman, Patrick M., Burnham, Jon M., Hakonarson, Hakon
Publicado 2016

Treatment of severe Kaposiform Lymphangiomatosis positive for NRAS mutation by MEK-inhibition

por Chowers, Guy, Abebe-Campino, Gadi, Golan, Hana, Vivante, Asaf, Greenberger, Shoshana, Soudack, Michalle, Barkai, Galia, Fox-Fisher, Ilana, Li, Dong, March, Michael, Battig, Mark R., Hakonarson, Hakon, Adams, Denise, Dori, Yoav, Dagan, Adi
Publicado 2022

Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders

por Glessner, Joseph T., Khan, Munir E., Chang, Xiao, Liu, Yichuan, Otieno, F. George, Lemma, Maria, Slaby, Isabella, Hain, Heather, Mentch, Frank, Li, Jin, Kao, Charlly, Sleiman, Patrick M. A., March, Michael E., Connolly, John, Hakonarson, Hakon
Publicado 2023