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61-70 trong số 143 kết quả
Genetic association studies using disease liabilities from deep neural networks
Tác giả: Lu Yang, Marie C Sadler, Russ B Altman
Xuất bản: United States: American journal of human genetics , 2025
Bộ sưu tập: NCBI
ddc:  006.32
 
LRP8 inhibits bladder cancer cell ferroptosis by activating the Wnt/β-catenin-SCD1 positive feedback loop
Tác giả: Yong Zhao, Guohong Shi, Xiang Huang, Zhongyuan Zhang, Kaijun Liao, Hao Xiong, Zhiqiang Feng, Shihui Mao, Xu Zhang
Xuất bản: England: Human molecular genetics , 2025
Bộ sưu tập: NCBI
ddc:  133.5265
 
Characterizing substructure via mixture modeling in large-scale genetic summary statistics
Tác giả: Hayley R Stoneman, Adelle M Price, Katie M Marker, Audrey E Hendricks, Nikole Scribner Trout, Riley Lamont, Souha Tifour, Nikita Pozdeyev, Kristy Crooks, Meng Lin, Nicholas Rafaels, Christopher R Gignoux
Xuất bản: United States: American journal of human genetics , 2025
Bộ sưu tập: NCBI
ddc:  003.71
 
Isogenic hiPSC models of Turner syndrome development reveal shared roles of inactive X and Y in the human cranial neural crest network
Tác giả: Darcy T Ahern, Prakhar Bansal, Isaac V Faustino, Owen M Chambers, Erin C Banda, Heather R Glatt-Deeley, Rachael E Massey, Yuvabharath Kondaveeti, Stefan F Pinter
Xuất bản: United States: American journal of human genetics , 2025
Bộ sưu tập: NCBI
ddc:  612.647
 
Contribution of autosomal rare and de novo variants to sex differences in autism
Tác giả: Mahmoud Koko, F Kyle Satterstrom, Varun Warrier, Hilary Martin
Xuất bản: United States: American journal of human genetics , 2025
Bộ sưu tập: NCBI
ddc:  155.33
 
Whole-genome sequencing reveals the impact of lipid pathway and APOE genotype on brain amyloidosis
Tác giả: Maulikkumar Patel, Cyril Pottier, Ann D Cohen, James T Becker, Beth E Snitz, Howard Aizenstein, Oscar L Lopez, John C Morris, M Ilyas Kamboh, Carlos Cruchaga, Kang-Hsien Fan, Arda Cetin, Matthew Johnson, Muhammad Ali, Menghan Liu, Priyanka Gorijala, John Budde, Ruyu Shi
Xuất bản: England: Human molecular genetics , 2025
Bộ sưu tập: NCBI
ddc:  612.826
 
Genetic analysis of elevated levels of creatinine and cystatin C biomarkers reveals novel genetic loci associated with k...
Tác giả: Matteo D'Antonio, Timothy D Arthur, Wilfredo G Gonzalez Rivera, Ximei Wu, Jennifer P Nguyen, Melissa Gymrek, Park Woo-Yeong, Kelly A Frazer
Xuất bản: England: Human molecular genetics , 2025
Bộ sưu tập: NCBI
ddc:  660.65
 
The chromatin remodeler Brg1 is essential for cochlear sensory epithelium differentiation and patterning
Tác giả: Yuning Song, Zhilin Dou, Wenwen Liu, Aizhen Zhang, Xiaotong Gao, Hongbiao Shi, Zhixiong Zhang, Jiangang Gao, Yecheng Jin
Xuất bản: England: Human molecular genetics , 2025
Bộ sưu tập: NCBI
ddc:  808.0428
 
Exome sequencing identifies HELB as a novel susceptibility gene for non-mucinous, non-high-grade-serous epithelial ovari...
Tác giả: Ed M Dicks, Jonthan P Tyrer, Toon Van Gorp, Anna De Fazio, David D L Bowtell, Dale W Garsed, Kunle Odunsi, Kirsten Moysich, Marina Pavanello, Florentia Fostira, Penelope M Webb, Jana Soukupová, Suzana Ezquina, Paul A Cohen, Weiva Sieh, Renée Turzanski Fortner, Charite Ricker, Beth Karlan, Ian Campbell, James D Brenton, Susan J Ramus, Simon A Gayther, Paul D P Pharoah, Michelle Jones, John Baierl, Pei-Chen Peng, Michael Diaz, Ellen Goode, Stacey J Winham, Thilo Dörk
Xuất bản: England: European journal of human genetics : EJHG , 2025
Bộ sưu tập: NCBI
ddc:  782.296
 
An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansio...
Tác giả: Koen C Demaegd, Aoife Kernan, Patrick A Dion, Guy A Rouleau, Andrea Western, Paul J Parsons, Benjamin Mclean, Michael Benatar, Leonard H van den Berg, Philip Van Damme, Jan Willem Dankbaar, Jeroen Hendrikse, Johnathan Cooper-Knock, Wouter Koole, Charlotte de Bie, Esther Hobson, Jan H Veldink, Bart van de Warrenburg, R Jeroen Pasterkamp, Wouter van Rheenen, Janine Kirby, Pamela J Shaw, Michael A van Es, Joke J F A van Vugt, Calum Harvey, Tobias Moll, David O'Brien, Sarah Gornall, Luke Drury, Sali M K Farhan
Xuất bản: England: European journal of human genetics : EJHG , 2025
Bộ sưu tập: NCBI
ddc:  959.3031
 

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