खोज परिणाम - Glessner, Joseph T.
- प्रदर्शित 1 - 20 परिणाम 129
- अगले पृष्ठ पर जाएँ
-
1
-
2
-
3
-
4
-
5
Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries द्वारा Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick, Hakonarson, Hakon
प्रकाशित 2022मूलपाठ -
6
-
7
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus द्वारा Sleiman, Patrick, Wang, Dai, Glessner, Joseph, Hadley, Dexter, Gur, Raquel E., Cohen, Nadine, Li, Qingqin, Hakonarson, Hakon
प्रकाशित 2013मूलपाठ -
8
Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects द्वारा Agopian, A. J., Mitchell, Laura E., Glessner, Joseph, Bhalla, Angela D., Sewda, Anshuman, Hakonarson, Hakon, Goldmuntz, Elizabeth
प्रकाशित 2014मूलपाठ -
9
Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries द्वारा Qu, Hui-Qi, Snyder, James, Connolly, John, Glessner, Joseph, Kao, Charlly, Sleiman, Patrick M.A., Hakonarson, Hakon
प्रकाशित 2022मूलपाठ -
10
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data द्वारा Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Glessner, Joseph, Sleiman, Patrick A. M., Hakonarson, Hakon
प्रकाशित 2022मूलपाठ -
11
An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities द्वारा Slaby, Isabella, Hain, Heather S., Abrams, Debra, Mentch, Frank D., Glessner, Joseph T., Sleiman, Patrick M. A., Hakonarson, Hakon
प्रकाशित 2022मूलपाठ -
12
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data द्वारा Wang, Kai, Li, Mingyao, Hadley, Dexter, Liu, Rui, Glessner, Joseph, Grant, Struan F.A., Hakonarson, Hakon, Bucan, Maja
प्रकाशित 2007मूलपाठ -
13
Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts द्वारा Connolly, John J., Glessner, Joseph T., Almoguera, Berta, Crosslin, David R., Jarvik, Gail P., Sleiman, Patrick M., Hakonarson, Hakon
प्रकाशित 2014मूलपाठ -
14
Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies द्वारा Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.
प्रकाशित 2011मूलपाठ -
15
Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa द्वारा Chang, Xiao, qu, Huiqi, Liu, Yichuan, Glessner, Joseph, Hou, Cuiping, Wang, Fengxiang, Li, Jin, Sleiman, Patrick, Hakonarson, Hakon
प्रकाशित 2019मूलपाठ -
16
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans द्वारा Chang, Xiao, Liu, Yichuan, Mentch, Frank, Glessner, Joseph, Qu, Huiqi, Nguyen, Kenny, Sleiman, Patrick M. A., Hakonarson, Hakon
प्रकाशित 2020मूलपाठ -
17
MONTAGE: a new tool for high-throughput detection of mosaic copy number variation द्वारा Glessner, Joseph T., Chang, Xiao, Liu, Yichuan, Li, Jin, Khan, Munir, Wei, Zhi, Sleiman, Patrick M. A., Hakonarson, Hakon
प्रकाशित 2021मूलपाठ -
18
-
19
-
20
Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters द्वारा Liu, Yichuan, Qu, Hui-Qi, Chang, Xiao, Tian, Lifeng, Qu, Jingchun, Glessner, Joseph, Sleiman, Patrick M. A., Hakonarson, Hakon
प्रकाशित 2021मूलपाठ