Yvette P. Conley - Publications

University of Pittsburgh, Pittsburgh, PA, United States 
Nursing, Genetics

94 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Kochanek PM, Jackson TC, Jha R, Clark RSB, Okonkwo DO, Bayir H, Poloyac SM, Wagner AK, Empey PE, Conley YP, Bell MJ, Kline AE, Bondi CO, Simon DW, Carlson SW, et al. Paths to successful translation of new therapies for severe TBI in the golden age of traumatic brain injury research: A Pittsburgh vision. Journal of Neurotrauma. PMID 30520681 DOI: 10.1089/neu.2018.6203  0.8
2016 Shih J, Leutwyler H, Ritchie C, Paul SM, Levine JD, Cooper B, Wright F, Conley YP, Miaskowski C. Characteristics associated with inter-individual differences in the trajectories of self-reported attentional function in oncology outpatients receiving chemotherapy. Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer. PMID 27766422 DOI: 10.1007/s00520-016-3461-2  0.8
2016 Wesmiller SW, Sereika SM, Bender CM, Bovbjerg D, Ahrendt G, Bonaventura M, Conley YP. Exploring the multifactorial nature of postoperative nausea and vomiting in women following surgery for breast cancer. Autonomic Neuroscience : Basic & Clinical. PMID 27729204 DOI: 10.1016/j.autneu.2016.09.017  0.8
2016 Jha RM, Puccio AM, Okonkwo DO, Zusman BE, Park SY, Wallisch J, Empey PE, Shutter LA, Clark RS, Kochanek PM, Conley YP. ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI. Neurocritical Care. PMID 27677908 DOI: 10.1007/s12028-016-0309-z  0.8
2016 Fu MR, Conley YP, Axelrod D, Guth AA, Yu G, Fletcher J, Zagzag D. Precision assessment of heterogeneity of lymphedema phenotype, genotypes and risk prediction. Breast (Edinburgh, Scotland). PMID 27460425 DOI: 10.1016/j.breast.2016.06.023  0.8
2016 Baumgartel KL, Groer MW, Cohen SM, Ren D, Spatz DL, Conley YP. Effect of Promoter Polymorphisms on Cytokine Concentration in Preterm Breast Milk and Subsequent Infant Outcomes. Journal of Human Lactation : Official Journal of International Lactation Consultant Association. PMID 27250867 DOI: 10.1177/0890334416646725  0.8
2016 Myrga JM, Juengst SB, Failla MD, Conley YP, Arenth PM, Grace AA, Wagner AK. COMT and ANKK1 Genetics Interact With Depression to Influence Behavior Following Severe TBI: An Initial Assessment. Neurorehabilitation and Neural Repair. PMID 27154305 DOI: 10.1177/1545968316648409  0.8
2016 Ritter AC, Kammerer CM, Brooks MM, Conley YP, Wagner AK. Genetic variation in neuronal glutamate transport genes and associations with posttraumatic seizure. Epilepsia. PMID 27153812 DOI: 10.1111/epi.13397  0.8
2016 Koleck TA, Bender CM, Sereika SM, Brufsky AM, Lembersky BC, McAuliffe PF, Puhalla SL, Rastogi P, Conley YP. Polymorphisms in DNA repair and oxidative stress genes associated with pre-treatment cognitive function in breast cancer survivors: an exploratory study. Springerplus. 5: 422. PMID 27099827 DOI: 10.1186/s40064-016-2061-4  0.8
2016 Koleck TA, Conley YP. Identification and prioritization of candidate genes for symptom variability in breast cancer survivors based on disease characteristics at the cellular level. Breast Cancer (Dove Medical Press). 8: 29-37. PMID 27022301 DOI: 10.2147/BCTT.S88434  0.8
2016 Martire LM, Wilson SJ, Small BJ, Conley YP, Janicki PK, Sliwinski MJ. COMT and OPRM1 Genotype Associations with Daily Knee Pain Variability and Activity Induced Pain. Scandinavian Journal of Pain. 10: 6-12. PMID 26322144 DOI: 10.1016/j.sjpain.2015.07.004  0.8
2015 Myrga JM, Failla MD, Ricker JH, Dixon CE, Conley YP, Arenth PM, Wagner AK. A Dopamine Pathway Gene Risk Score for Cognitive Recovery Following Traumatic Brain Injury: Methodological Considerations, Preliminary Findings, and Interactions With Sex. The Journal of Head Trauma Rehabilitation. PMID 26580694 DOI: 10.1097/HTR.0000000000000199  0.8
2015 Henly SJ, McCarthy DO, Wyman JF, Alt-White AC, Stone PW, McCarthy AM, Redeker NS, Dunbar-Jacob J, Titler MG, Conley YP, Heitkemper MM, Moore SM. Emerging areas of nursing science and PhD education for the 21(st) century: Response to commentaries. Nursing Outlook. 63: 439-45. PMID 26187083 DOI: 10.1016/j.outlook.2015.05.003  0.8
2015 Henly SJ, McCarthy DO, Wyman JF, Stone PW, Redeker NS, McCarthy AM, Alt-White AC, Dunbar-Jacob J, Titler MG, Moore SM, Heitkemper MM, Conley YP. Integrating emerging areas of nursing science into PhD programs. Nursing Outlook. 63: 408-16. PMID 26187080 DOI: 10.1016/j.outlook.2015.04.010  0.8
2015 Henly SJ, McCarthy DO, Wyman JF, Heitkemper MM, Redeker NS, Titler MG, McCarthy AM, Stone PW, Moore SM, Alt-White AC, Conley YP, Dunbar-Jacob J. Emerging areas of science: Recommendations for Nursing Science Education from the Council for the Advancement of Nursing Science Idea Festival. Nursing Outlook. 63: 398-407. PMID 26187079 DOI: 10.1016/j.outlook.2015.04.007  0.8
2015 Hafrén L, Einarsdottir E, Kentala E, Hammarén-Malmi S, Bhutta MF, MacArthur CJ, Wilmot B, Casselbrant M, Conley YP, Weeks DE, Mandel EM, Vaarala O, Kallio A, Melin M, Nieminen JK, et al. Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus. Plos One. 10: e0132551. PMID 26177520 DOI: 10.1371/journal.pone.0132551  0.8
2015 Diamond ML, Ritter AC, Failla MD, Boles JA, Conley YP, Kochanek PM, Wagner AK. IL-1β associations with posttraumatic epilepsy development: A genetics and biomarker cohort study. Epilepsia. 56: 991-1001. PMID 26149793 DOI: 10.1111/epi.13100  0.8
2015 Conley YP, Heitkemper M, McCarthy D, Anderson CM, Corwin EJ, Daack-Hirsch S, Dorsey SG, Gregory KE, Groer MW, Henly SJ, Landers T, Lyon DE, Taylor JY, Voss J. Educating future nursing scientists: Recommendations for integrating omics content in PhD programs. Nursing Outlook. PMID 26123776 DOI: 10.1016/j.outlook.2015.06.006  0.8
2015 Bui DK, Jiang Y, Wei X, Ortube MC, Weeks DE, Conley YP, Gorin MB. Genetic ME-a visualization application for merging and editing pedigrees for genetic studies. Bmc Research Notes. 8: 241. PMID 26076732 DOI: 10.1186/s13104-015-1131-y  0.8
2015 Diamond ML, Ritter AC, Jackson EK, Conley YP, Kochanek PM, Boison D, Wagner AK. Genetic variation in the adenosine regulatory cycle is associated with posttraumatic epilepsy development. Epilepsia. PMID 26040919 DOI: 10.1111/epi.13044  0.8
2015 Failla MD, Conley YP, Wagner AK. Brain-Derived Neurotrophic Factor (BDNF) in Traumatic Brain Injury-Related Mortality: Interrelationships Between Genetics and Acute Systemic and Central Nervous System BDNF Profiles. Neurorehabilitation and Neural Repair. PMID 25979196 DOI: 10.1177/1545968315586465  0.8
2015 Failla MD, Myrga JM, Ricker JH, Dixon CE, Conley YP, Wagner AK. Posttraumatic Brain Injury Cognitive Performance Is Moderated by Variation Within ANKK1 and DRD2 Genes. The Journal of Head Trauma Rehabilitation. PMID 25931179 DOI: 10.1097/HTR.0000000000000118  0.8
2015 Donnelly MK, Crago EA, Conley YP, Balzer JR, Ren D, Ducruet AF, Kochanek PM, Sherwood PR, Poloyac SM. 20-HETE is associated with unfavorable outcomes in subarachnoid hemorrhage patients. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 35: 1515-22. PMID 25920956 DOI: 10.1038/jcbfm.2015.75  0.8
2015 Baron RV, Conley YP, Gorin MB, Weeks DE. dbVOR: a database system for importing pedigree, phenotype and genotype data and exporting selected subsets. Bmc Bioinformatics. 16: 91. PMID 25887129 DOI: 10.1186/s12859-015-0505-4  0.8
2015 Dunn SH, Conley YP. A systematic review of genetic influences on coping. Biological Research For Nursing. 17: 87-93. PMID 25504954 DOI: 10.1177/1099800414527340  0.8
2015 Donnelly MK, Conley YP, Crago EA, Ren D, Sherwood PR, Balzer JR, Poloyac SM. Genetic markers in the EET metabolic pathway are associated with outcomes in patients with aneurysmal subarachnoid hemorrhage. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 35: 267-76. PMID 25388680 DOI: 10.1038/jcbfm.2014.195  0.8
2015 Hopkins EE, Wallace ML, Conley YP, Marazita ML. Symptoms of attention-deficit hyperactivity disorder, nonsyndromic orofacial cleft children, and dopamine polymorphisms: a pilot study. Biological Research For Nursing. 17: 257-62. PMID 25271118 DOI: 10.1177/1099800414552186  0.8
2015 Failla MD, Kumar RG, Peitzman AB, Conley YP, Ferrell RE, Wagner AK. Variation in the BDNF gene interacts with age to predict mortality in a prospective, longitudinal cohort with severe TBI. Neurorehabilitation and Neural Repair. 29: 234-46. PMID 25063686 DOI: 10.1177/1545968314542617  0.8
2015 Conley YP. Genomic, transcriptomic, epigenomic, and proteomic approaches Routledge International Handbook of Advanced Quantitative Methods in Nursing Research. 324-335.  0.8
2014 Koleck TA, Bender CM, Sereika SM, Ahrendt G, Jankowitz RC, McGuire KP, Ryan CM, Conley YP. Apolipoprotein E genotype and cognitive function in postmenopausal women with early-stage breast cancer. Oncology Nursing Forum. 41: E313-25. PMID 25355028 DOI: 10.1188/14.ONF.E313-E325  0.8
2014 Diamond ML, Boles JA, Ritter AC, Failla MD, Conley YP, Kochanek PM, Wagner AK. In response to comments on IL-1β associations with posttraumatic epilepsy development: a genetics and biomarker cohort study. Epilepsia. 55: 1313-4. PMID 25099304 DOI: 10.1111/epi.12714  0.8
2014 Wagner AK, Scanlon JM, Becker CR, Ritter AC, Niyonkuru C, Dixon CE, Conley YP, Price JC. The influence of genetic variants on striatal dopamine transporter and D2 receptor binding after TBI. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 34: 1328-39. PMID 24849661 DOI: 10.1038/jcbfm.2014.87  0.8
2014 Diamond ML, Ritter AC, Failla MD, Boles JA, Conley YP, Kochanek PM, Wagner AK. IL-1β associations with posttraumatic epilepsy development: a genetics and biomarker cohort study. Epilepsia. 55: 1109-19. PMID 24754437 DOI: 10.1111/epi.12628  0.8
2014 Alexander SA, Ren D, Gunn SR, Kochanek PM, Tate J, Ikonomovic M, Conley YP. Interleukin 6 and apolipoprotein E as predictors of acute brain dysfunction and survival in critical care patients. American Journal of Critical Care : An Official Publication, American Association of Critical-Care Nurses. 23: 49-57. PMID 24382617 DOI: 10.4037/ajcc2014578  0.8
2014 Kantor E, Bayır H, Ren D, Provencio JJ, Watkins L, Crago E, Horowitz MB, Ferrell RE, Conley YP, Alexander SA. Haptoglobin genotype and functional outcome after aneurysmal subarachnoid hemorrhage. Journal of Neurosurgery. 120: 386-90. PMID 24286153 DOI: 10.3171/2013.10.JNS13219  0.8
2014 Conley YP, Okonkwo DO, Deslouches S, Alexander S, Puccio AM, Beers SR, Ren D. Mitochondrial polymorphisms impact outcomes after severe traumatic brain injury. Journal of Neurotrauma. 31: 34-41. PMID 23883111 DOI: 10.1089/neu.2013.2855  0.8
2013 Zhan X, Larson DE, Wang C, Koboldt DC, Sergeev YV, Fulton RS, Fulton LL, Fronick CC, Branham KE, Bragg-Gresham J, Jun G, Hu Y, Kang HM, Liu D, Othman M, ... ... Conley YP, et al. Identification of a rare coding variant in complement 3 associated with age-related macular degeneration. Nature Genetics. 45: 1375-9. PMID 24036949 DOI: 10.1038/ng.2758  0.8
2013 Cousar JL, Conley YP, Willyerd FA, Sarnaik AA, Puccio AM, Empey PE, Kochanek PM, Bell MJ, Okonkwo DO, Clark RS. Influence of ATP-binding cassette polymorphisms on neurological outcome after traumatic brain injury. Neurocritical Care. 19: 192-8. PMID 23896815 DOI: 10.1007/s12028-013-9881-7  0.8
2013 Failla MD, Burkhardt JN, Miller MA, Scanlon JM, Conley YP, Ferrell RE, Wagner AK. Variants of SLC6A4 in depression risk following severe TBI. Brain Injury. 27: 696-706. PMID 23672445 DOI: 10.3109/02699052.2013.775481  0.8
2013 Bell MJ, Roberts JM, Founds SA, Jeyabalan A, Terhorst L, Conley YP. Variation in endoglin pathway genes is associated with preeclampsia: a case-control candidate gene association study. Bmc Pregnancy and Childbirth. 13: 82. PMID 23548068 DOI: 10.1186/1471-2393-13-82  0.8
2013 Garringer JA, Niyonkuru C, McCullough EH, Loucks T, Dixon CE, Conley YP, Berga S, Wagner AK. Impact of aromatase genetic variation on hormone levels and global outcome after severe TBI. Journal of Neurotrauma. 30: 1415-25. PMID 23540392 DOI: 10.1089/neu.2012.2565  0.8
2013 Conley YP, Biesecker LG, Gonsalves S, Merkle CJ, Kirk M, Aouizerat BE. Current and emerging technology approaches in genomics. Journal of Nursing Scholarship : An Official Publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau. 45: 5-14. PMID 23294727 DOI: 10.1111/jnu.12001  0.8
2013 Baumgartel KL, Conley YP. The utility of breastmilk for genetic or genomic studies: a systematic review. Breastfeeding Medicine : the Official Journal of the Academy of Breastfeeding Medicine. 8: 249-56. PMID 23259645 DOI: 10.1089/bfm.2012.0054  0.8
2013 Baumgartel KL, Terhorst L, Conley YP, Roberts JM. Psychometric evaluation of the Epworth sleepiness scale in an obstetric population. Sleep Medicine. 14: 116-21. PMID 23218535 DOI: 10.1016/j.sleep.2012.10.007  0.8
2013 Darrah SD, Miller MA, Ren D, Hoh NZ, Scanlon JM, Conley YP, Wagner AK. Genetic variability in glutamic acid decarboxylase genes: associations with post-traumatic seizures after severe TBI. Epilepsy Research. 103: 180-94. PMID 22840783 DOI: 10.1016/j.eplepsyres.2012.07.006  0.8
2013 Henker RA, Lewis A, Dai F, Lariviere WR, Meng L, Gruen GS, Sereika SM, Pape H, Tarkin IS, Gowda I, Conley YP. The associations between OPRM 1 and COMT genotypes and postoperative pain, opioid use, and opioid-induced sedation. Biological Research For Nursing. 15: 309-17. PMID 22718527 DOI: 10.1177/1099800411436171  0.8
2013 Wesmiller SW, Henker RA, Sereika SM, Donovan HS, Meng L, Gruen GS, Tarkin IS, Conley YP. The association of CYP2D6 genotype and postoperative nausea and vomiting in orthopedic trauma patients. Biological Research For Nursing. 15: 382-9. PMID 22718526 DOI: 10.1177/1099800412449181  0.8
2013 Bell MJ, Conley YP. A systematic review of endoglin gene expression in preeclampsia. Biological Research For Nursing. 15: 129-36. PMID 21921088 DOI: 10.1177/1099800411420133  0.8
2012 Founds SA, Shi H, Conley YP, Jeyabalan A, Roberts JM, Lyons-Weiler J. Variations in discovery-based preeclampsia candidate genes. Clinical and Translational Science. 5: 333-9. PMID 22883611 DOI: 10.1111/j.1752-8062.2012.00413.x  0.8
2012 Wagner AK, Hatz LE, Scanlon JM, Niyonkuru C, Miller MA, Ricker JH, Conley YP, Ferrell RE. Association of KIBRA rs17070145 polymorphism and episodic memory in individuals with severe TBI. Brain Injury. 26: 1658-69. PMID 22794909 DOI: 10.3109/02699052.2012.700089  0.8
2012 Sofat R, Casas JP, Webster AR, Bird AC, Mann SS, Yates JR, Moore AT, Sepp T, Cipriani V, Bunce C, Khan JC, Shahid H, Swaroop A, Abecasis G, Branham KE, ... ... Conley YP, et al. Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. International Journal of Epidemiology. 41: 250-62. PMID 22253316 DOI: 10.1093/ije/dyr204  0.8
2011 Baumgartel K, Zelazny J, Timcheck T, Snyder C, Bell M, Conley YP. Molecular genomic research designs. Annual Review of Nursing Research. 29: 1-26. PMID 22891496 DOI: 10.1891/0739-6686.29.1  0.8
2011 Chiu CJ, Conley YP, Gorin MB, Gensler G, Lai CQ, Shang F, Taylor A. Associations between genetic polymorphisms of insulin-like growth factor axis genes and risk for age-related macular degeneration. Investigative Ophthalmology & Visual Science. 52: 9099-107. PMID 22058336 DOI: 10.1167/iovs.11-7782  0.8
2011 Williams JK, Prows CA, Conley YP, Eggert J, Kirk M, Nichols F. Strategies to prepare faculty to integrate genomics into nursing education programs. Journal of Nursing Scholarship : An Official Publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau. 43: 231-8. PMID 21884368 DOI: 10.1111/j.1547-5069.2011.01401.x  0.8
2011 Conley YP, Alexander S. Genomic, transcriptomic, and epigenomic approaches to recovery after acquired brain injury. Pm & R : the Journal of Injury, Function, and Rehabilitation. 3: S52-8. PMID 21703581 DOI: 10.1016/j.pmrj.2011.04.004  0.8
2011 Sanders JL, Iannaccone A, Boudreau RM, Conley YP, Opresko PL, Hsueh WC, Cummings SR, Cawthon RM, Harris TB, Nalls MA, Kritchevsky SB, Newman AB. The association of cataract with leukocyte telomere length in older adults: defining a new marker of aging. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 66: 639-45. PMID 21382885 DOI: 10.1093/gerona/glr034  0.8
2011 Charles BA, Conley YP, Chen G, Miller RG, Dorman JS, Gorin MB, Ferrell RE, Sereika SM, Rotimi CN, Orchard TJ. Variants of the adenosine A(2A) receptor gene are protective against proliferative diabetic retinopathy in patients with type 1 diabetes. Ophthalmic Research. 46: 1-8. PMID 21088442 DOI: 10.1159/000317057  0.8
2011 Founds SA, Terhorst LA, Conrad KP, Hogge WA, Jeyabalan A, Conley YP. Gene expression in first trimester preeclampsia placenta. Biological Research For Nursing. 13: 134-9. PMID 21044967 DOI: 10.1177/1099800410385448  0.8
2010 Soliday FK, Conley YP, Henker R. Pseudocholinesterase deficiency: a comprehensive review of genetic, acquired, and drug influences. Aana Journal. 78: 313-20. PMID 20879632  0.8
2010 Founds SA, Fallert-Junecko B, Reinhart TA, Conley YP, Parks WT. LAIR2 localizes specifically to sites of extravillous trophoblast invasion Placenta. 31: 880-885. PMID 20692035 DOI: 10.1016/j.placenta.2010.07.005  0.8
2010 Wagner AK, Miller MA, Scanlon J, Ren D, Kochanek PM, Conley YP. Adenosine A1 receptor gene variants associated with post-traumatic seizures after severe TBI. Epilepsy Research. 90: 259-72. PMID 20609566 DOI: 10.1016/j.eplepsyres.2010.06.001  0.8
2010 Hoh NZ, Wagner AK, Alexander SA, Clark RB, Beers SR, Okonkwo DO, Ren D, Conley YP. BCL2 genotypes: functional and neurobehavioral outcomes after severe traumatic brain injury. Journal of Neurotrauma. 27: 1413-27. PMID 20504155 DOI: 10.1089/neu.2009.1256  0.8
2010 Chuang PY, Conley YP, Poloyac SM, Okonkwo DO, Ren D, Sherwood PR, Hravnak M, Alexander SA. Neuroglobin genetic polymorphisms and their relationship to functional outcomes after traumatic brain injury. Journal of Neurotrauma. 27: 999-1006. PMID 20345238 DOI: 10.1089/neu.2009.1129  0.8
2010 Sarnaik AA, Conley YP, Okonkwo DO, Barr TL, Fink EL, Szabo C, Kochanek PM, Clark RS. Influence of PARP-1 polymorphisms in patients after traumatic brain injury. Journal of Neurotrauma. 27: 465-71. PMID 19925161 DOI: 10.1089/neu.2009.1171  0.8
2009 Conley YP. Genetics and genomics in nursing research. Biological Research For Nursing. 11: 5-6. PMID 19546130 DOI: 10.1177/1099800409336293  0.8
2009 Dungan JR, Conley YP, Langaee TY, Johnson JA, Kneipp SM, Hess PJ, Yucha CB. Altered beta-2 adrenergic receptor gene expression in human clinical hypertension. Biological Research For Nursing. 11: 17-26. PMID 19254913 DOI: 10.1177/1099800409332538  0.8
2009 Jakobsdottir J, Gorin MB, Conley YP, Ferrell RE, Weeks DE. Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers. Plos Genetics. 5: e1000337. PMID 19197355 DOI: 10.1371/journal.pgen.1000337  0.8
2009 Conley YP, Mukherjee A, Kammerer C, DeKosky ST, Kamboh MI, Finegold DN, Ferrell RE. Evidence supporting a role for the calcium-sensing receptor in Alzheimer disease. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 703-9. PMID 19035514 DOI: 10.1002/ajmg.b.30896  0.8
2009 Gallek MJ, Conley YP, Sherwood PR, Horowitz MB, Kassam A, Alexander SA. APOE genotype and functional outcome following aneurysmal subarachnoid hemorrhage. Biological Research For Nursing. 10: 205-12. PMID 19017669 DOI: 10.1177/1099800408323221  0.8
2008 Alexander SA, Kerr ME, Balzer J, Horowitz M, Kassam A, Kim Y, Hoffman L, Conley YP. Cerebrospinal fluid apolipoprotein E, calcium and cerebral vasospasm after subarachnoid hemorrhage. Biological Research For Nursing. 10: 102-12. PMID 18829593 DOI: 10.1177/1099800408321722  0.8
2008 Sarnaik AA, Conley YP, Clark RS. Susceptibility to meningococcal infection--nature versus nurture? Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies. 9: 540-2. PMID 18779704 DOI: 10.1097/PCC.0b013e3181849e62  0.8
2008 Jakobsdottir J, Conley YP, Weeks DE, Ferrell RE, Gorin MB. C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes. Plos One. 3: e2199. PMID 18493315 DOI: 10.1371/journal.pone.0002199  0.8
2008 Founds SA, Dorman JS, Conley YP. Microarray technology applied to the complex disorder of preeclampsia. Journal of Obstetric, Gynecologic, and Neonatal Nursing : Jognn / Naacog. 37: 146-57. PMID 18336438 DOI: 10.1111/j.1552-6909.2008.00232.x  0.8
2007 Barr TL, Conley YP. Poly(ADP-ribose) polymerase-1 and its clinical applications in brain injury. The Journal of Neuroscience Nursing : Journal of the American Association of Neuroscience Nurses. 39: 278-84. PMID 17966294 DOI: 10.1097/01376517-200710000-00004  0.8
2007 Alexander S, Kerr ME, Kim Y, Kamboh MI, Beers SR, Conley YP. Apolipoprotein E4 allele presence and functional outcome after severe traumatic brain injury. Journal of Neurotrauma. 24: 790-7. PMID 17518534 DOI: 10.1089/neu.2006.0133  0.8
2007 Wagner AK, Ren D, Conley YP, Ma X, Kerr ME, Zafonte RD, Puccio AM, Marion DW, Dixon CE. Sex and genetic associations with cerebrospinal fluid dopamine and metabolite production after severe traumatic brain injury. Journal of Neurosurgery. 106: 538-47. PMID 17432702 DOI: 10.3171/jns.2007.106.4.538  0.8
2007 Conley YP, Tinkle MB. The future of genomic nursing research. Journal of Nursing Scholarship : An Official Publication of Sigma Theta Tau International Honor Society of Nursing / Sigma Theta Tau. 39: 17-24. PMID 17393961 DOI: 10.1111/j.1547-5069.2007.00138.x  0.8
2007 Rodway GW, Sethi JM, Hoffman LA, Conley YP, Choi AM, Sereika SM, Zullo TG, Ryter SW, Sanders MH. Hemodynamic and molecular response to intermittent hypoxia (IH) versus continuous hypoxia (CH) in normal humans. Translational Research : the Journal of Laboratory and Clinical Medicine. 149: 76-84. PMID 17240318 DOI: 10.1016/j.trsl.2006.09.005  0.8
2006 Conley YP, Jakobsdottir J, Mah T, Weeks DE, Klein R, Kuller L, Ferrell RE, Gorin MB. CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Human Molecular Genetics. 15: 3206-18. PMID 17000705 DOI: 10.1093/hmg/ddl396  0.8
2005 Jakobsdottir J, Conley YP, Weeks DE, Mah TS, Ferrell RE, Gorin MB. Susceptibility genes for age-related maculopathy on chromosome 10q26. American Journal of Human Genetics. 77: 389-407. PMID 16080115 DOI: 10.1086/444437  0.8
2005 Fisher SA, Abecasis GR, Yashar BM, Zareparsi S, Swaroop A, Iyengar SK, Klein BE, Klein R, Lee KE, Majewski J, Schultz DW, Klein ML, Seddon JM, Santangelo SL, Weeks DE, ... Conley YP, et al. Meta-analysis of genome scans of age-related macular degeneration. Human Molecular Genetics. 14: 2257-64. PMID 15987700 DOI: 10.1093/hmg/ddi230  0.8
2005 Conley YP, Thalamuthu A, Jakobsdottir J, Weeks DE, Mah T, Ferrell RE, Gorin MB. Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy. Human Molecular Genetics. 14: 1991-2002. PMID 15930014 DOI: 10.1093/hmg/ddi204  0.8
2004 Conley YP, Steele AM, Puskar KR. Genetic susceptibility to psychiatric disorders. Medsurg Nursing : Official Journal of the Academy of Medical-Surgical Nurses. 13: 319-25. PMID 15587131  0.8
2004 Baysal BE, DeLoia JA, Willett-Brozick JE, Goodman MT, Brady MF, Modugno F, Lynch HT, Conley YP, Watson P, Gallion HH. Analysis of CHEK2 gene for ovarian cancer susceptibility. Gynecologic Oncology. 95: 62-9. PMID 15385111 DOI: 10.1016/j.ygyno.2004.07.015  0.8
2004 Weeks DE, Conley YP, Tsai HJ, Mah TS, Schmidt S, Postel EA, Agarwal A, Haines JL, Pericak-Vance MA, Rosenfeld PJ, Paul TO, Eller AW, Morse LS, Dailey JP, Ferrell RE, et al. Age-related maculopathy: a genomewide scan with continued evidence of susceptibility loci within the 1q31, 10q26, and 17q25 regions. American Journal of Human Genetics. 75: 174-89. PMID 15168325 DOI: 10.1086/422476  0.8
2003 Conley YP, Brockway H, Beatty M, Kerr ME. Qualitative and quantitative detection of mitochondrial heteroplasmy in cerebrospinal fluid using denaturing high-performance liquid chromatography. Brain Research. Brain Research Protocols. 12: 99-103. PMID 14613811 DOI: 10.1016/j.brainresprot.2003.08.005  0.8
2002 Schmidt S, Klaver C, Saunders A, Postel E, De La Paz M, Agarwal A, Small K, Udar N, Ong J, Chalukya M, Nesburn A, Kenney C, Domurath R, Hogan M, Mah T, ... Conley Y, et al. A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathy. Ophthalmic Genetics. 23: 209-23. PMID 12567264 DOI: 10.1076/opge.  0.8
2002 Conley YP, Finegold DN. Exploring calcium level disorders. Looking through the genetic window for new treatment clues. Awhonn Lifelines / Association of Women's Health, Obstetric and Neonatal Nurses. 6: 424-9. PMID 12420385  0.8
2002 Weeks DE, Conley YP, Ferrell RE, Mah TS, Gorin MB. A tale of two genotypes: consistency between two high-throughput genotyping centers. Genome Research. 12: 430-5. PMID 11875031 DOI: 10.1101/gr.211502  0.8
2001 Weeks DE, Conley YP, Tsai HJ, Mah TS, Rosenfeld PJ, Paul TO, Eller AW, Morse LS, Dailey JP, Ferrell RE, Gorin MB. Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions. American Journal of Ophthalmology. 132: 682-92. PMID 11704029 DOI: 10.1016/S0002-9394(01)01214-4  0.8
2000 Conley YP, Finegold DN, Peters DG, Cook JS, Oppenheim DS, Ferrell RE. Three novel activating mutations in the calcium-sensing receptor responsible for autosomal dominant hypocalcemia. Molecular Genetics and Metabolism. 71: 591-8. PMID 11136551 DOI: 10.1006/mgme.2000.3096  0.8
2000 Weeks DE, Conley YP, Mah TS, Paul TO, Morse L, Ngo-Chang J, Dailey JP, Ferrell RE, Gorin MB. A full genome scan for age-related maculopathy. Human Molecular Genetics. 9: 1329-49. PMID 10814715  0.8
2000 Conley YP, Erturk D, Keverline A, Mah TS, Keravala A, Barnes LR, Bruchis A, Hess JF, FitzGerald PG, Weeks DE, Ferrell RE, Gorin MB. A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. American Journal of Human Genetics. 66: 1426-31. PMID 10729115 DOI: 10.1086/302871  0.8
1996 Johnson K, Mintz-Hittner HA, Conley YP, Ferrell RE. X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease protein Clinical Genetics. 50: 113-115. PMID 8946107  0.8
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