Kategorie: DDC-Klasse 599.935

5297 Titel

• Pediatric Whole Exome Sequencing: an Assessment of Parents’ Perceived and Actual Understanding
  Tolusso, Leandra K. ; Collins, Kathleen ; Zhang, Xue ; Holle, Jennifer R. ; Alexander Valencia, C. ; Myers, Melanie F.
• Counselees’ Perspectives of Genomic Counseling Following Online Receipt of Multiple Actionable Complex Disease and Pharmacogenomic Results: a Qualitative Research Study
  Sweet, Kevin ; Hovick, Shelly ; Sturm, Amy C. ; Schmidlen, Tara ; Gordon, Erynn ; Bernhardt, Barbara ; Wawak, Lisa ; Wernke, Karen ; McElroy, Joseph ; Scheinfeldt, Laura ; Toland, Amanda E. ; Roberts, J. S. ; Christman, Michael
• Assessment of copy number variations in 120 patients with Poland syndrome
  Vaccari, Carlotta Maria ; Tassano, Elisa ; Torre, Michele ; Gimelli, Stefania ; Divizia, Maria Teresa ; Romanini, Maria Victoria ; Bossi, Simone ; Musante, Ilaria ; Valle, Maura ; Senes, Filippo ; Catena, Nunzio ; Bedeschi, Maria Francesca ; Baban, Anwar ; Calevo, Maria Grazia ; Acquaviva, Massimo ; Lerone, Margherita ; Ravazzolo, Roberto ; Puliti, Aldamaria
• microRNA-27a rs895819 is associated with obesity in HIV infected preeclamptic Black South African women on HAART
  Maharaj, Niren Ray ; Ramkaran, Prithiksha ; Pillay, Siddharthiya ; Chuturgoon, Anil Amichund
• My Identical Twin Sequenced our Genome
  Schilit, Samantha L.P ; Schilit Nitenson, Arielle
• Teaching Genetic Counseling Skills: Incorporating a Genetic Counseling Adaptation Continuum Model to Address Psychosocial Complexity
  Shugar, Andrea
• Lifestyle Risk Factors for Breast Cancer in BRCA1/2-Mutation Carriers Around Childbearing Age
  Erkelens, A. van ; Derks, L. ; Sie, A. S. ; Egbers, L. ; Woldringh, G. ; Prins, J. B. ; Manders, P. ; Hoogerbrugge, N.
• Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes
  Wong, John K. L. ; Campbell, Desmond ; Ngo, Ngoc Diem ; Yeung, Fanny ; Cheng, Guo ; Tang, Clara S. M. ; Chung, Patrick H. Y. ; Tran, Ngoc Son ; So, Man-ting ; Cherny, Stacey S. ; Sham, Pak C. ; Tam, Paul K. ; Garcia-Barcelo, Maria-Mercè
• Patient Perspectives on Intimate Partner Violence Discussion during Genetic Counseling Sessions
  Chen, Christina ; Greb, Anne ; Kalia, Isha ; Bajaj, Komal ; Klugman, Susan
• A single nucleotide polymorphism in the UMOD promoter is associated with end stage renal disease
  Chen, Tingyu ; Wang, Qianliao ; Li, Guisen ; Wang, Li
• Translation and adaptation of skin cancer genomic risk education materials for implementation in primary care
  Rodriguez, Vivian M. ; Robers, Erika ; Zielaskowski, Kate ; Javier González, C. ; Hunley, Keith ; Kaphingst, Kimberly A. ; Guest, Dolores D. ; Sussman, Andrew ; Meyer White, Kirsten A. ; Schwartz, Matthew R. ; Greb, Jennie ; Talamantes, Yvonne ; Bigney, Jessica ; Berwick, Marianne ; Hay, Jennifer L.
• Genetic Counseling Assistants: an Integral Piece of the Evolving Genetic Counseling Service Delivery Model
  Pirzadeh-Miller, Sara ; Robinson, Linda S. ; Read, Parker ; Ross, Theodora S.
• DNA methylation patterns associated with oxidative stress in an ageing population
  Hedman, Åsa K. ; Zilmer, Mihkel ; Sundström, Johan ; Lind, Lars ; Ingelsson, Erik
• Genetic Counselor Practices Involving Pediatric Patients with FAP: an Investigation of their Self-Reported Strategies for Genetic Testing and Hepatoblastoma Screening
  Lawson, Caitlin E. ; Attard, Thomas M. ; Dai, Hongying ; Septer, Seth
• Physical activity and sedentary behavior can modulate the effect of the PNPLA3 variant on childhood NAFLD: a case-control study in a Chinese population
  Wang, Shuo ; Song, Jieyun ; Shang, Xiaorui ; Chawla, Nitesh ; Yang, Yide ; Meng, Xiangrui ; Wang, Haijun ; Ma, Jun
• VDBP, CYP27B1, and 25-Hydroxyvitamin D Gene Polymorphism Analyses in a Group of Sicilian Multiple Sclerosis Patients
  Agnello, L. ; Scazzone, C. ; Lo Sasso, B. ; Bellia, C. ; Bivona, G. ; Realmuto, S. ; Brighina, F. ; Schillaci, R. ; Ragonese, P. ; Salemi, G. ; Ciaccio, Marcello
• Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency
  Bergendal, Birgitta ; Norderyd, Johanna ; Zhou, Xiaolei ; Klar, Joakim ; Dahl, Niklas
• Effect of Pregnane X Receptor*1B genetic polymorphisms on postoperative analgesia with fentanyl in Chinese patients undergoing gynecological surgery
  Yuan, Jing-Jing ; Ma, Xiao-jing ; Li, Zhi-Song ; Chang, Yan-Zi ; Zhang, Wei ; Kan, Quan-Cheng ; Hou, Jun-Kai ; Zhang, Li-rong
• “A rising tide lifts all boats”: establishing a multidisciplinary genomic tumor board for breast cancer patients with advanced disease
  McGowan, Michelle L. ; Ponsaran, Roselle S. ; Silverman, Paula ; Harris, Lyndsay N. ; Marshall, Patricia A.
• A qualitative study of patients’ perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH)
  Hallowell, Nina ; Jenkins, Nicholas ; Douglas, Margaret ; Walker, Simon ; Finnie, Robert ; Porteous, Mary ; Lawton, Julia