Search Results - "JENKINS, Sharon"

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy by QUARTA, Giovanni, SYRRIS, Petros, ASHWORTH, Michael, JENKINS, Sharon, ZUBORNE ALAPI, Krisztina, MORGAN, John, MUIR, Alison, PANTAZIS, Antonios, MCKENNA, William J, ELLIOTT, Perry M

“…Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease predominantly caused by mutations in desmosomal protein genes…”
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Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing by Lopes, Luis R, Zekavati, Anna, Syrris, Petros, Hubank, Mike, Giambartolomei, Claudia, Dalageorgou, Chrysoula, Jenkins, Sharon, McKenna, William, Plagnol, Vincent, Elliott, Perry M

“…Clinical interpretation of the large number of rare variants identified by high throughput sequencing (HTS) technologies is challenging. The aim of this study…”
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Interpersonal Decentering and Person-Situation Interaction in the Thematic Apperception Test: Is It all in the Cards? What's the Story? by Rae Jenkins, Sharon, Siefert, Caleb J., Weber, Katherine

“…Assessors using storytelling assessment techniques have debated the relative importance of picture imagery (card pull) versus story content for interpreting…”
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Clinical considerations in the psychological evaluation of gestational surrogates: uses of narrative assessment by Riddle, Mary P., Jenkins, Sharon R.

“…Potential risks and ethical considerations inherent in surrogacy arrangements place tremendous responsibility on mental health professionals performing the…”
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Stabilization of Cu(I) for binding and calorimetric measurements in aqueous solution by Johnson, Destinee K, Stevenson, Michael J, Almadidy, Zayed A, Jenkins, Sharon E, Wilcox, Dean E, Grossoehme, Nicholas E

“…Conditions have been developed for the comproportionation reaction of Cu(2+) and copper metal to prepare aqueous solutions of Cu(+) that are stabilized from…”
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Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB―FKBPL―NOTCH4 region of chromosome 6p21.3 by CIPRIANI, Valentina, LEUNG, Hin-Tak, CAMPBELL, Susan, ARMBRECHT, Ana Maria, DHILLON, Baljean, DEARY, Ian J, CAMPBELL, Harry, DUNLOP, Malcolm, DOMINICZAK, Anna F, MANN, Samantha S, JENKINS, Sharon A, WEBSTER, Andrew R, PLAGNOL, Vincent, BIRD, Alan C, LATHROP, Mark, ZELENIKA, Diana, SOUIED, Eric H, SAHEL, José-Alain, LEVEILLARD, Thierry, CREE, Angela J, GIBSON, Jane, ENNIS, Sarah, LOTERY, Andrew J, BUNCE, Catey, WRIGHT, Alan F, CLAYTON, David G, YATES, John R. W, KHAN, Jane C, SHAHID, Humma, MOORE, Anthony T, HARDING, Simon P, BISHOP, Paul N, HAYWARD, Caroline

“…Age-related macular degeneration (AMD) is a leading cause of visual loss in Western populations. Susceptibility is influenced by age, environmental and genetic…”
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Parental Overprotection, Cultural Value Conflict, and Psychological Adaptation among Asian Indian Women in America by Varghese, Anita, Rae Jenkins, Sharon

“…The present study related generational status, marital status, parental overprotection (control), and cultural value conflict to self-esteem and depression…”
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Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriers by van Rijsingen, Ingrid A.W., Nannenberg, Eline A., Arbustini, Eloisa, Elliott, Perry M., Mogensen, Jens, Hermans-van Ast, Johanna F., van der Kooi, Anneke J., van Tintelen, J. Peter, van den Berg, Maarten P., Grasso, Maurizia, Serio, Alessandra, Jenkins, Sharon, Rowland, Camilla, Richard, Pascale, Wilde, Arthur A.M., Perrot, Andreas, Pankuweit, Sabine, Zwinderman, Aeilko H., Charron, Philippe, Christiaans, Imke, Pinto, Yigal M.

“…Aims Mutations in the lamin A/C gene (LMNA) cause a variety of clinical phenotypes, including dilated cardiomyopathy. LMNA is one of the most prevalent mutated…”
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Thematic Apperceptive Techniques Inform a Science of Individuality by Rae Jenkins, Sharon

“…This special section of Rorschachiana presents eight papers that describe and apply formal, interscorer reliable systems for thematic apperceptive techniques…”
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Differential Performance of Professional Dancers to the Music Apperception Test and the Thematic Apperception Test by van den Daele, Leland, Yates, Ashley, Rae Jenkins, Sharon

“…This project compared the relative performance of professional dancers and nondancers on the Music Apperception Test (MAT; van den Daele, 2014), then compared…”
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Mutations in the Gene Coding for the Pre-mRNA Splicing Factor, PRPF31, in Patients with Autosomal Dominant Retinitis Pigmentosa by Waseem, Naushin H, Vaclavik, Veronika, Webster, Andrew, Jenkins, Sharon A, Bird, Alan C, Bhattacharya, Shomi S

“…Retinitis pigmentosa is a clinically and genetically heterogeneous disorder. It is characterized by progressive degeneration of the peripheral retina, leading…”
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Measuring teacher beliefs about curriculum orientations using the modified-curriculum orientations inventory by Jenkins, Sharon Billburg

“…Although curriculum orientations are widely discussed in educational literature, the extent to which teachers and other educational specialists in the United…”
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Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans by Wu, Huimin, Cowing, Jill A., Michaelides, Michel, Wilkie, Susan E., Jeffery, Glen, Jenkins, Sharon A., Mester, Viktoria, Bird, Alan C., Robson, Anthony G., Holder, Graham E., Moore, Anthony T., Hunt, David M., Webster, Andrew R.

“…“Cone dystrophy with supernormal rod electroretinogram (ERG)” is an autosomal recessive disorder that causes lifelong visual loss combined with a supernormal…”
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The symmetry of phenotype between eyes of patients with early and late bilateral age-related macular degeneration (AMD) by Mann, Samantha S., Rutishauser-Arnold, Yvonne, Peto, Tunde, Jenkins, Sharon A., Leung, Irene, Xing, Wen, Bird, Alan C., Bunce, Catey, Webster, Andrew R.

“…Background Macular degeneration is known to be a bilateral disease. This study set out to determine the symmetry of phenotype between eyes of patients with…”
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Identification of Novel RPGR ORF15 Mutations in X-linked Progressive Cone-Rod Dystrophy (XLCORD) Families by Ebenezer, Neil D, Michaelides, Michel, Jenkins, Sharon A, Audo, Isabelle, Webster, Andrew R, Cheetham, Michael E, Stockman, Andrew, Maher, Eamonn R, Ainsworth, John R, Yates, John R, Bradshaw, Keith, Holder, Graham E, Moore, Anthony T, Hardcastle, Alison J

“…To test the incidence of mutations in RPGR ORF15 in six families with X-linked progressive retinal degeneration (cone-rod dystrophy [XLCORD], macular or cone…”
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Maculopathy Due to the R345W Substitution in Fibulin-3: Distinct Clinical Features, Disease Variability, and Extent of Retinal Dysfunction by Michaelides, Michel, Jenkins, Sharon A, Brantley, Milam A., Jr, Andrews, Richard M, Waseem, Naushin, Luong, Vy, Gregory-Evans, Kevin, Bhattacharya, Shomi S, Fitzke, Fred W, Webster, Andrew R

“…To determine (1) clinical features that distinguish maculopathy due to the R345W substitution in fibulin-3 from other forms of inherited or early-onset drusen,…”
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A Strong First Step: Comment on Krishnamurthy et al. (2022) by Jenkins, Sharon Rae

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Managing Alzheimer’s Dementia with Homecare in an African American Family During the COVID Pandemic by Eversley, Rani, Favila, Wendy, Jenkins, Sharon Rae, Godwin, Makula, Pedrosa, Maria

“…In the US, over 95 million people have been infected with COVID and over 1 million have died. 10% of Californians are infected with COVID with higher rates…”
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Vicarious traumatization, secondary traumatic stress, and burnout in sexual assault and domestic violence agency staff by Baird, Stephanie, Jenkins, Sharon Rae

“…This study investigated three occupational hazards of therapy with trauma victims: vicarious trauma and secondary traumatic stress (or "compassion fatigue"),…”
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Pseudoxanthoma Elasticum with Generalized Retinal Dysfunction, a Common Finding? by Audo, Isabelle, Vanakker, Olivier M, Smith, Alaric, Leroy, Bart P, Robson, Anthony G, Jenkins, Sharon A, Coucke, Paul J, Bird, Alan C, De Paepe, Anne, Holder, Graham E, Webster, Andrew R

“…Pseudoxanthoma elasticum (PXE; [MIM 264800]) is an autosomal recessive systemic disorder characterized by progressive degeneration and calcification of elastic…”
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