Results 171 to 180 of about 97,365 (285)

Highly Parallel SNP Genotyping

Cold Spring Harbor Symposia on Quantitative Biology, 2003
Kevin L. Gunderson, Arnold Oliphant, Francisco Garcia, Eliza Wickham, W Chang, Dennis Doucet, David Bentley, Panagiotis Deloukas, Philippe Rigault, D Campbell, Frank J. Steemers, M S Chee, S L Butler, Jennifer S. Haas, L Zhou, J Chen, Richard Shen, J Stuelpnagel, Baohong Zhang, Bahram Ghaffarzadeh Kermani, Jian-Bing Fan, Todd Rubano, Mark Hansen, Celeste McBride, Semyon Kruglyak, Marina Bibikova, Sarah E. Hunt, Luana Galver   +27 more
openaire   +2 more sources

From multi‐omics to precision medicine in intracranial aneurysm: Biomarker discovery and multimodal integration

Interdisciplinary Medicine, EarlyView.
This review explores intracranial aneurysm biomarker discovery through multi‐omics. It reveals key genes, proteins, and metabolites, and shows how machine‐learning‐based multi‐modal integration may aid diagnosis and treatment. Abstract Despite extensive research, currently, no biomarkers are available for clinical use in intracranial aneurysm (IA ...
Jiaxin Zhang, Yufei Yang, Bingxu Chen, Yanmeng Zhao, Haitao Sun   +4 more
wiley   +1 more source

Faculty Opinions recommendation of L-RCA (ligation-rolling circle amplification): a general method for genotyping of single nucleotide polymorphisms (SNPs).

, 2001
Peter Langridge
openalex   +2 more sources

Prenatal Diagnosis, Ultrasound Findings, and Follow‐Up Evaluation of 16p13.11 Deletion and Duplication Syndromes: Preliminary Assessment of Fetal Genotype–Phenotype

Journal of Clinical Laboratory Analysis, EarlyView.
What do the results of this study add? We expanded the clinical phenotype spectrum of fetuses with 16p13.11 deletion and duplication and conducted a preliminary evaluation of prenatal ultrasound findings in conjunction with postnatal clinical phenotypes. The primary manifestations observed in fetuses with 16p13.11 deletion and duplication are likely to
Xiaojin Luo, Liping Wu, Jinshuang Song, Jinmao Xu, Ruchun Huang, Hongyan Niu, Fei Zhou, Yuanyuan Pei, Weiqiang Liu, Fengxiang Wei   +9 more
wiley   +1 more source

A genotype calling algorithm for affymetrix SNP arrays [PDF]

, 2005
Nusrat Rabbee, Terence P. Speed
openalex   +1 more source

Intergenerational transmission of attachment: The role of intelligence

JCPP Advances, EarlyView.
Attachment and cognitive development are associated, but the direction of the association is unclear. Recently, Del Giudice and Haltigan have argued that attachment in childhood and attachment representations in adulthood are influenced by the cognitive capabilities of the individual, which might make the intergenerational transmission of attachment ...
Jana Runze, Marinus H. Van IJzendoorn, Annemieke M. Witte, Charlotte A. M. Cecil, Marian J. Bakermans‐Kranenburg   +4 more
wiley   +1 more source

Impact of placental and peripheral blood DNA methylation on celiac disease susceptibility

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Several studies suggest that the first immunogenic insult in celiac disease (CeD) could occur during fetal development. The placenta is a key organ that could link the environment with the genome and future outcomes, including CeD.
Alba Hernangomez‐Laderas, Ariadna Cilleros‐Portet, Mikel de la Peña‐Sanz, Sergi Marí, Corina Lesseur, Itziar González‐Moro, Bárbara P. González‐García, Jia Chen, Iraia García‐Santisteban, Carmen J. Marsit, Jose Ramon Bilbao, Nora Fernandez‐Jimenez   +11 more
wiley   +1 more source

Investigating the bHLH transcription factor TSARL1 as marker and regulator of saponin biosynthesis in Chenopodium quinoa

Journal of the Science of Food and Agriculture, EarlyView.
Abstract BACKGROUND Quinoa (Chenopodium quinoa) is valued for its nutritional benefits and resilience to abiotic stresses. However, its commercial use is limited by bitter‐tasting saponins on the seeds, necessitating resource‐intensive removal processes.
Marius Kollmar, Katharina B. Böndel, Lukas John, Stefan Arold, Karl Schmid, David Jarvis, Sandra M Schmöckel, Sophie L Otterbach   +7 more
wiley   +1 more source

Detection of genotyping errors and pseudo‐SNPs via deviations from Hardy‐Weinberg equilibrium [PDF]

, 2005
Suzanne M. Leal
openalex   +1 more source

GCKR Polymorphisms Increase the Risks of Low Bone Mineral Density in Young and Non‐Obese Patients With MASLD and Hyperuricemia

The Kaohsiung Journal of Medical Sciences, Volume 41, Issue 6, June 2025.
ABSTRACT Metabolic‐associated steatotic liver disease (MASLD) encompasses common comorbidities including low bone mineral density (BMD) and hyperuricemia (HU), yet relevant genetic analyses are limited. This study aimed to investigate the genetic effects of risk single nucleotide polymorphisms (SNPs) on the occurrence of low BMD in patients with MASLD ...
Tzu‐Hao Li, Yu‐Shin Huang, Chia‐Chen Ma, Shin‐Yu Tsai, Hung‐Cheng Tsai, Hsiao‐Yun Yeh, Hsiao‐Chin Shen, Shiao‐Ya Hong, Chien‐Wei Su, Hwai‐I Yang, Ying‐Ying Yang, Ming‐Chih Hou   +11 more
wiley   +1 more source