Search Results - "Medical genetics

Genetic Causal Relationship Between Sex Hormones and Basal Cell Carcinoma: A Two-Sample Mendelian Randomization Study by Luo P, Gao D, Wang C, Guo R, Zhang Q

Connect to this object online.

Genetic Variants, Circulating Level of MCP1 with Risk of Chronic Obstructive Pulmonary Disease: A Case-Control Study by Lin C, Wang Z, Shen L, Yi G, Li M, Li D

Connect to this object online.

f-treeGC: a questionnaire-based family tree-creation software for genetic counseling and genome cohort studies by Tomoharu Tokutomi, Akimune Fukushima, Kayono Yamamoto, Yasushi Bansho, Tsuyoshi Hachiya, Atsushi Shimizu

Connect to this object online.

Interactive Web-Based Resource for Annotation of Genetic Variants Causing Hereditary Angioedema (HADA): Database Development, Implementation, and Validation by Mendoza-Alvarez, Alejandro, Muñoz-Barrera, Adrián, Rubio-Rodríguez, Luis Alberto, Marcelino-Rodriguez, Itahisa, Corrales, Almudena, Iñigo-Campos, Antonio, Callero, Ariel, Perez-Rodriguez, Eva, Garcia-Robaina, Jose Carlos, González-Montelongo, Rafaela, Lorenzo-Salazar, Jose Miguel, Flores, Carlos

Connect to this object online.

Genetic algorithm-assisted machine learning for clinical pregnancy prediction in in vitro fertilizationAJOG Global Reports at a Glance by Claudio Michael Louis, SKom, BEng, Nining Handayani, DVM, MBiomed, Tri Aprilliana, BPH, Arie A. Polim, MD, SpOG, DMAS, MBHRE, Arief Boediono, DVM, PhD, Ivan Sini, MD, FRANZOG, GDRM, MMIS, SpOG

Connect to this object online.

Genetic variant I148M in <it>PNPLA3</it> is associated with the ultrasonography-determined steatosis degree in a Chinese population by Li Yiling, Xing Chao, Tian Zhong, Ku Hung-Chih

Connect to this object online.

Investigation of RBC Indices and HbA2 Levels in Parents of Beta-Thalassemia Patients: Impacts on Premarital Genetic Counseling by Mina Izadyar, Jila Dastan, Tayebeh Sabokbar, Solmaz Shoraka, Azadeh Shojaei, Habib Nasiri, Saeed Reza Ghaffari

Connect to this object online.

Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study by Pantel, Jean Tori, Hajjir, Nurulhuda, Danyel, Magdalena, Elsner, Jonas, Abad-Perez, Angela Teresa, Hansen, Peter, Mundlos, Stefan, Spielmann, Malte, Horn, Denise, Ott, Claus-Eric, Mensah, Martin Atta

Connect to this object online.

The frequency of CYP2C19 genetic polymorphisms in Russian patients with peptic ulcers treated with proton pump inhibitors by Sychev DA, Denisenko NP, Sizova ZM, Grachev AV, Velikolug KA

Connect to this object online.

Association of Genetic Variants in miR-217 Gene with Risk of Coronary Artery Disease: A Case–Control Study by Han X, Liang X, Wu M, Zhang L, Jiang H

Connect to this object online.

Genetic Polymorphisms in Serotonin Transporter (5HTT) and Catechol-O-Methyltransferase (COMT) On Dental Implant Loss - Pilot Project by Thais Mariana Neves CHAVES, Paula Cruz Porto SPADA, Michelle Nascimento EGER, Marilisa Carneiro Leão GABARDO, João César ZIELAK, Tatiana Miranda DELIBERADOR, João Armando BRANCHER

Connect to this object online.

PREGNANCY AND DELIVERY IN WOMAN AFTER IVF WITH COMBINED THROMBOPHILIA (CIRCULATION OF ANTIPHOSPHOLIPID ANTIBODIES AND GENETIC THROMBOPHILIA) AND MULTIPLY IVF FAILURES by N. S. Stuleva

Connect to this object online.

Genotype-phenotype correlation in Jordanian children with genetically-proven familial Mediterranean fever: The effect of R202Q mutation by Eyad Altamimi, Dua` N. Samara, Dima Bani Issa, Saied Jaradat, Wail Hayajneh

Connect to this object online.

Genetic Variants of CYP4F2 Associated with Ischemic Stroke Susceptibility in the Han Population from Southern China by Huang K, Ma T, Li Q, Zhou Y, Qin T, Zhong Z, Tang S, Zhang W, Zhong J, Lu S

Connect to this object online.

Evaluation of the Rosa Chatbot Providing Genetic Information to Patients at Risk of Hereditary Breast and Ovarian Cancer: Qualitative Interview Study by Elen Siglen, Hildegunn Høberg Vetti, Mirjam Augestad, Vidar M Steen, Åshild Lunde, Cathrine Bjorvatn

Connect to this object online.

Application of Y-STR, DIP-STR and SNP-STR Markers in Interpretation of Forensic Genetic Profiling: A Narrative Review by Mehdi Forozesh, Shiva Irani, Azam Soleimani, Seyed Jalil Monabati

Connect to this object online.

Genome-wide analysis of retinal transcriptome reveals common genetic network underlying perception of contrast and optical defocus detection by Tatiana V. Tkatchenko, Andrei V. Tkatchenko

Connect to this object online.

Prospective multicenter observational the personalized therapy with clopidogrel for stenting in acute coronary syndrome regarding the genetic polymorphisms (PROTOCOL) study by G. I. Lifshits, K. A. Apartsin

Connect to this object online.

An Accurate and Inter-Operatable Fuzzy-Based System Using Genetic and Canonical Correlation Analysis Methods in Internet-of-Brain Things by Geetanjali Rathee, Chaker Abdelaziz Kerrache, Muhammad Bilal

Connect to this object online.

Novel biallelic variant in BBS9 causative of Bardet-Biedl syndrome: expanding the spectrum of disease-causing genetic alterations by Julia Suárez-González, Verónica Seidel, Cristina Andrés-Zayas, Elvira Izquierdo, Ismael Buño

Connect to this object online.