Year |
Citation |
Score |
2015 |
Peterson EA, Jenkins EC, Lofgren KA, Chandiramani N, Liu H, Aranda E, Barnett M, Kenny PA. Amphiregulin Is a Critical Downstream Effector of Estrogen Signaling in ERα-Positive Breast Cancer. Cancer Research. PMID 26527289 DOI: 10.1158/0008-5472.Can-15-0709 |
0.609 |
|
2014 |
Jenkins EC, Debnath S, Varriano S, Gundry S, Fata JE. Na(+) /H(+) exchanger 1 (NHE1) function is necessary for maintaining mammary tissue architecture. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 243: 229-42. PMID 24038847 DOI: 10.1002/Dvdy.24032 |
0.642 |
|
2012 |
Fata JE, Debnath S, Jenkins EC, Fournier MV. Nongenomic Mechanisms of PTEN Regulation. International Journal of Cell Biology. 2012: 379685. PMID 22536248 DOI: 10.1155/2012/379685 |
0.633 |
|
2012 |
Jenkins EC, Debnath S, Gundry S, Gundry S, Uyar U, Fata JE. Intracellular pH regulation by Na⁺/H⁺ exchanger-1 (NHE1) is required for growth factor-induced mammary branching morphogenesis. Developmental Biology. 365: 71-81. PMID 22366186 DOI: 10.1016/J.Ydbio.2012.02.010 |
0.633 |
|
2010 |
Jenkins EC, Gundry S, Fata JE. NHE1: A Novel Determinant in Branching Morphogenesis Developmental Biology. 344: 446. DOI: 10.1016/J.Ydbio.2010.05.138 |
0.58 |
|
Low-probability matches (unlikely to be authored by this person) |
2019 |
Gomez ML, Shah N, Kenny TC, Jenkins EC, Germain D. SOD1 is essential for oncogene-driven mammary tumor formation but dispensable for normal development and proliferation. Oncogene. PMID 31222103 DOI: 10.1038/s41388-019-0839-x |
0.294 |
|
2022 |
Jenkins EC, Chattopadhyay M, Gomez M, Torre D, Ma'ayan A, Torres-Martin M, Sia D, Germain D. Age alters the oncogenic trajectory toward luminal mammary tumors that activate unfolded proteins responses. Aging Cell. e13665. PMID 36111352 DOI: 10.1111/acel.13665 |
0.264 |
|
2020 |
Jenkins EC, Brown SO, Germain D. The Multi-Faced Role of PAPP-A in Post-Partum Breast Cancer: IGF-Signaling is Only the Beginning. Journal of Mammary Gland Biology and Neoplasia. PMID 32901383 DOI: 10.1007/s10911-020-09456-1 |
0.231 |
|
2010 |
Huo LR, Ju W, Yan M, Zou JH, Yan W, He B, Zhao XL, Jenkins EC, Brown WT, Zhong N. Identification of differentially expressed transcripts and translatants targeted by knock-down of endogenous PCBP1. Biochimica Et Biophysica Acta. 1804: 1954-64. PMID 20624489 DOI: 10.1016/j.bbapap.2010.07.002 |
0.223 |
|
2013 |
Luo X, Shi Q, Gu Y, Pan J, Hua M, Liu M, Dong Z, Zhang M, Wang L, Gu Y, Zhong J, Zhao X, Jenkins EC, Brown WT, Zhong N. LncRNA pathway involved in premature preterm rupture of membrane (PPROM): an epigenomic approach to study the pathogenesis of reproductive disorders. Plos One. 8: e79897. PMID 24312190 DOI: 10.1371/journal.pone.0079897 |
0.208 |
|
2015 |
Luo X, Pan J, Wang L, Wang P, Zhang M, Liu M, Dong Z, Meng Q, Tao X, Zhao X, Zhong J, Ju W, Gu Y, Jenkins EC, Brown WT, et al. Epigenetic regulation of lncRNA connects ubiquitin-proteasome system with infection-inflammation in preterm births and preterm premature rupture of membranes. Bmc Pregnancy and Childbirth. 15: 35. PMID 25884766 DOI: 10.1186/s12884-015-0460-0 |
0.205 |
|
2021 |
Jenkins EC, Chattopadhyay M, Germain D. Are the estrogen receptor and SIRT3 axes of the mitochondrial UPR key regulators of breast cancer sub-type determination according to age? Aging and Cancer. 2: 75-81. PMID 34927079 DOI: 10.1002/aac2.12035 |
0.203 |
|
2021 |
Jenkins EC, O'Connell MJ, Manfredi G, Germain D. Doxycycline promotes proteasome fitness in the central nervous system. Scientific Reports. 11: 17003. PMID 34417525 DOI: 10.1038/s41598-021-96540-z |
0.175 |
|
2011 |
Wang P, Ju W, Wu D, Wang L, Yan M, Zou J, He B, Jenkins EC, Brown WT, Zhong N. A two-dimensional protein fragmentation-proteomic study of neuronal ceroid lipofuscinoses: identification and characterization of differentially expressed proteins. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences. 879: 304-16. PMID 21242110 DOI: 10.1016/j.jchromb.2010.12.011 |
0.158 |
|
2012 |
Wang L, Yang W, Ju W, Wang P, Zhao X, Jenkins EC, Brown WT, Zhong N. A proteomic study of Hutchinson-Gilford progeria syndrome: Application of 2D-chromotography in a premature aging disease. Biochemical and Biophysical Research Communications. 417: 1119-26. PMID 22210539 DOI: 10.1016/j.bbrc.2011.12.056 |
0.141 |
|
2020 |
Jenkins EC, Shah N, Gomez M, Casalena G, Zhao D, Kenny TC, Guariglia SR, Manfredi G, Germain D. Proteasome mapping reveals sexual dimorphism in tissue-specific sensitivity to protein aggregations. Embo Reports. e48978. PMID 32090465 DOI: 10.15252/Embr.201948978 |
0.136 |
|
1996 |
Dobkin CS, Nolin SL, Cohen I, Sudhalter V, Bialer MG, Ding XH, Jenkins EC, Zhong N, Brown WT. Tissue differences in fragile X mosaics: Mosaicism in blood cells may differ greatly from skin American Journal of Medical Genetics. 64: 296-301. PMID 8844069 DOI: 10.1002/(SICI)1096-8628(19960809)64:2<296::AID-AJMG13>3.0.CO;2-A |
0.134 |
|
2010 |
Kerkel K, Schupf N, Hatta K, Pang D, Salas M, Kratz A, Minden M, Murty V, Zigman WB, Mayeux RP, Jenkins EC, Torkamani A, Schork NJ, Silverman W, Croy BA, et al. Altered DNA methylation in leukocytes with trisomy 21. Plos Genetics. 6: e1001212. PMID 21124956 DOI: 10.1371/Journal.Pgen.1001212 |
0.13 |
|
2015 |
Pan J, Mor G, Ju W, Zhong J, Luo X, Aldo PB, Zhong M, Yu Y, Jenkins EC, Brown WT, Zhong N. Viral Infection-Induced Differential Expression of LncRNAs Associated with Collagen in Mouse Placentas and Amniotic Sacs. American Journal of Reproductive Immunology (New York, N.Y. : 1989). 74: 237-257. PMID 26073538 DOI: 10.1111/aji.12406 |
0.129 |
|
1976 |
Evans LA, Kevin M, Jenkins EC. Sister chromatid exchange and methylazoxymethanol acetate Mutation Research. 38. |
0.127 |
|
2011 |
Shen C, Zhao XL, Ju W, Zou XB, Huo LR, Yan W, Zou JH, Yan GD, Jenkins EC, Brown WT, Zhong N. A proteomic investigation of B lymphocytes in an autistic family: a pilot study of exposure to natural rubber latex (NRL) may lead to autism. Journal of Molecular Neuroscience : Mn. 43: 443-52. PMID 20957522 DOI: 10.1007/s12031-010-9463-5 |
0.126 |
|
1975 |
Jenkins EC, Curcuru Giordano FM, Krishna SG. A case report of 46,XX,t(4;13)(q31;q14) Birth Defects, Orig.Art.Ser.. 11: 332. |
0.118 |
|
2022 |
Chattopadhyay M, Jenkins EC, Lechuga-Vieco AV, Nie K, Fiel MI, Rialdi A, Guccione E, Enriquez JA, Sia D, Lujambio A, Germain D. The portrait of liver cancer is shaped by mitochondrial genetics. Cell Reports. 38: 110254. PMID 35045282 DOI: 10.1016/j.celrep.2021.110254 |
0.116 |
|
1994 |
Faso L, Trowbridge RS, Quan W, Yao XL, Jenkins EC, Maciulis A, Bunch TD, Wisniewski HM. Characterization of a strain of cerebral endothelial cells derived from goat brain which retain their differentiated traits after long-term passage. In Vitro Cellular & Developmental Biology. Animal. 30: 226-35. PMID 8069445 DOI: 10.1007/BF02632044 |
0.115 |
|
1994 |
Yao XL, Jenkins EC, Wisniewski HM. Effect of aluminum chloride on mitogenesis, mitosis, and cell cycle in human short-term whole blood cultures: lower concentrations enhance mitosis. Journal of Cellular Biochemistry. 54: 473-7. PMID 8014196 DOI: 10.1002/Jcb.240540414 |
0.114 |
|
2009 |
Mazur-Kolecka B, Cohen IL, Jenkins EC, Flory M, Merz G, Ted Brown W, Frackowiak J. Sera from children with autism alter proliferation of human neuronal progenitor cells exposed to oxidation. Neurotoxicity Research. 16: 87-95. PMID 19526302 DOI: 10.1007/s12640-009-9052-y |
0.111 |
|
2020 |
Jenkins EC, Casalena G, Gomez M, Zhao D, Kenny TC, Shah N, Manfredi G, Germain D. Raloxifene is a female-specific proteostasis therapeutic in the spinal cord. Endocrinology. PMID 33269387 DOI: 10.1210/endocr/bqaa221 |
0.11 |
|
1995 |
Jenkins EC, Houck GE, Ding XH, Li SY, Stark-Houck SL, Salerno J, Genovese M, Glicksman A, Nolin SL, Zhong N, Sklower Brooks SL, Dobkin CS, Brown WT. An update on fragile X prenatal diagnosis: End of the cytogenetic testing era Developmental Brain Dysfunction. 8: 293-301. |
0.109 |
|
1996 |
Brown WT, Houck GE, Ding X, Zhong N, Nolin S, Glicksman A, Dobkin C, Jenkins EC. Reverse mutations in the fragile X syndrome American Journal of Medical Genetics. 64: 287-292. PMID 8844067 DOI: 10.1002/(SICI)1096-8628(19960809)64:2<287::AID-AJMG11>3.0.CO;2-B |
0.108 |
|
1994 |
Sherman SL, Maddalena A, Howard-Peebles PN, Brown WT, Nolin S, Jenkins E, Schwartz C, Tarrelton J, Shapiro LR, Smits AP. Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses. American Journal of Medical Genetics. 51: 503-6. PMID 7943029 DOI: 10.1002/Ajmg.1320510442 |
0.106 |
|
1988 |
Devine-Gage EA, Jenkins EC, Brown WT, Robakis NK, Wisniewski HM. The genetics of Familial Alzheimer's Disease Age. 11: 98-102. DOI: 10.1007/Bf02431747 |
0.106 |
|
2014 |
Wang H, Cao Q, Ge J, Liu C, Ma Y, Meng Y, Wang Y, Zhao X, Liu R, Li C, Wang Y, Zhong J, Ju W, Jenkins EC, Brown WT, et al. LncRNA-regulated infection and inflammation pathways associated with pregnancy loss: genome wide differential expression of lncRNAs in early spontaneous abortion. American Journal of Reproductive Immunology (New York, N.Y. : 1989). 72: 359-75. PMID 24916667 DOI: 10.1111/aji.12275 |
0.106 |
|
2005 |
Ramakrishna N, Meeker C, Li S, Jenkins EC, Currie JR, Flory M, Lee B, Liu MS, Miller DL. Polymerase chain reaction method to identify Down syndrome model segmentally trisomic mice. Analytical Biochemistry. 340: 213-9. PMID 15840493 DOI: 10.1016/j.ab.2005.02.002 |
0.103 |
|
2009 |
Velinov M, Novelli A, Gu H, Fenko M, Dolzhanskaya N, Bernardini L, Capalbo A, Dallapiccola B, Jenkins EC, Brown WT. De-novo 2.15 Mb terminal Xq duplication involving MECP2 but not L1CAM gene in a male patient with mental retardation. Clinical Dysmorphology. 18: 9-12. PMID 19090026 DOI: 10.1097/MCD.0b013e3283157cad |
0.102 |
|
1986 |
Jenkins EC, Brown WT, Brooks J, Duncan CJ, Sanz MM, Silverman WP, Lele KP, Masia A, Katz E, Lubin RA. Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanation. Experimental Cell Biology. 54: 40-8. PMID 3956839 DOI: 10.1159/000163342 |
0.101 |
|
2004 |
Velinov M, Gu H, Genovese M, Duncan C, Warburton P, Brooks SS, Jenkins EC. Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses Annales De Genetique. 47: 199-205. PMID 15183754 DOI: 10.1016/j.anngen.2004.02.005 |
0.101 |
|
2006 |
Jenkins EC, Jenkins EC, Genovese M, Wen GY. The effect of colcemid and aluminum on the ultrastructure of human metaphase chromosomes. Scanning. 28: 228-32. PMID 16898670 |
0.1 |
|
2007 |
Mazur-Kolecka B, Cohen IL, Jenkins EC, Kaczmarski W, Flory M, Frackowiak J. Altered development of neuronal progenitor cells after stimulation with autistic blood sera. Brain Research. 1168: 11-20. PMID 17706942 DOI: 10.1016/j.brainres.2007.06.084 |
0.099 |
|
1985 |
Devine EA, Nolin SL, Houck GE, Jenkins EC, Brown WT. Chromosomal localization of several families of repetitive sequences by in situ hybridization American Journal of Human Genetics. 37: 114-123. PMID 3976654 |
0.098 |
|
2005 |
Velinov M, Kupferman J, Gu H, Macera MJ, Babu A, Jenkins EC, Kupchik G. Polycystic kidneys and del (4)(q21.1q21.3): Further delineation of a distinct phenotype European Journal of Medical Genetics. 48: 51-55. PMID 15953406 DOI: 10.1016/j.ejmg.2005.01.008 |
0.096 |
|
2012 |
Jenkins EC, Tassone F, Ye L, Hoogeveen AT, Brown WT, Hagerman RJ, Hagerman PJ. Reduced telomere length in individuals with FMR1 premutations and full mutations. American Journal of Medical Genetics. Part A. 158: 1060-5. PMID 22489017 DOI: 10.1002/Ajmg.A.35275 |
0.095 |
|
1992 |
Hsu LYF, Kaffe S, Jenkins EC, Alonso L, Benn PA, David K, Hirschhorn K, Lieber E, Shanske A, Shapiro LR, Schutta E, Warburton D. Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies Prenatal Diagnosis. 12: 555-573. PMID 1508847 |
0.095 |
|
1998 |
Brooks SS, Genovese M, Gu H, Duncan CJ, Shanske A, Jenkins EC. Normal adaptive function with learning disability in duplication 8p including band p22 American Journal of Medical Genetics. 78: 114-117. PMID 9674899 DOI: 10.1002/(SICI)1096-8628(19980630)78:2<114::AID-AJMG3>3.0.CO;2-O |
0.095 |
|
2003 |
Cohen IL, Liu X, Schutz C, White BN, Jenkins EC, Brown WT, Holden JJ. Association of autism severity with a monoamine oxidase A functional polymorphism. Clinical Genetics. 64: 190-7. PMID 12919132 DOI: 10.1034/J.1399-0004.2003.00115.X |
0.095 |
|
1991 |
Fisch GS, Silverman W, Jenkins EC. Genetic and other factors that contribute to variability in cytogenetic expression in fragile X males American Journal of Medical Genetics. 38: 404-407. PMID 2018081 DOI: 10.1002/ajmg.1320380250 |
0.094 |
|
1991 |
Jacky PB, Ahuja YR, Anyane-Yeboa K, Breg WR, Carpenter NJ, Froster-Iskenius UG, Fryns JP, Glover TW, Gustavson KH, Hoegerman SF, Holmgren G, Howard-Peebles PN, Jenkins EC, Krawczun MS, Neri G, et al. Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes American Journal of Medical Genetics. 38: 400-403. PMID 2018080 DOI: 10.1002/ajmg.1320380249 |
0.092 |
|
2021 |
Jenkins EC, Chattopadhyay M, Germain D. Folding Mitochondrial-Mediated Cytosolic Proteostasis Into the Mitochondrial Unfolded Protein Response. Frontiers in Cell and Developmental Biology. 9: 715923. PMID 34631705 DOI: 10.3389/fcell.2021.715923 |
0.091 |
|
1986 |
Sklower SL, Jenkins EC, Anderson ML, Chan CB, Brown WT. Variability of thymidylate synthase activity in whole blood cultures treated with FUdR American Journal of Medical Genetics. 23: 483-490. PMID 2937302 |
0.091 |
|
2012 |
Jenkins EC, Ye L, Velinov M, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Mild cognitive impairment identified in older individuals with Down syndrome by reduced telomere signal numbers and shorter telomeres measured in microns. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 598-604. PMID 22592955 DOI: 10.1002/Ajmg.B.32066 |
0.091 |
|
2011 |
Barua M, Jenkins EC, Chen W, Kuizon S, Pullarkat RK, Junaid MA. Glyoxalase I polymorphism rs2736654 causing the Ala111Glu substitution modulates enzyme activity--implications for autism. Autism Research : Official Journal of the International Society For Autism Research. 4: 262-70. PMID 21491613 DOI: 10.1002/aur.197 |
0.09 |
|
1992 |
Erster SH, Ted Brown W, Goonewardena P, Dobkin CS, Jenkins EC, Pergolizzi RG. Polymerase chain reaction analysis of fragile X mutations Human Genetics. 90: 55-61. PMID 1427787 DOI: 10.1007/BF00210744 |
0.09 |
|
2009 |
Zhang YX, Zhang YP, Gu Y, Guan FJ, Li SL, Xie JS, Shen Y, Wu BL, Ju W, Jenkins EC, Brown WT, Zhong N. Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH. Clinical Genetics. 75: 133-40. PMID 19215247 DOI: 10.1111/j.1399-0004.2008.01131.x |
0.09 |
|
1992 |
Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome. American Journal of Medical Genetics. 43: 136-41. PMID 1605182 DOI: 10.1002/ajmg.1320430121 |
0.089 |
|
1994 |
Jenkins EC, Morys I, Henderson J, Genovese M, Carter M, Li SY, Houck GE, Ding X, Stark-Houck SL, Dobkin CS, Brown WT. Fragile X induction systems in CVS cultures: Effect on cytogenetic, PCR, and genomic Southern blot DNA analyses of the FMR-1 gene American Journal of Medical Genetics. 51: 436-442. PMID 7943013 DOI: 10.1002/ajmg.1320510426 |
0.088 |
|
2020 |
Zions M, Meehan EF, Kress ME, Thevalingam D, Jenkins EC, Kaila K, Puskarjov M, McCloskey DP. Nest Carbon Dioxide Masks GABA-Dependent Seizure Susceptibility in the Naked Mole-Rat. Current Biology : Cb. PMID 32359429 DOI: 10.1016/J.Cub.2020.03.071 |
0.088 |
|
2008 |
Velinov M, Beldia G, Gu H, Tsiouris JA, Jenkins EC, Brown WT. Psychotic manifestations in a patient with mental retardation and a 6.2 megabase deletion at the distal short arm of chromosome 12. Cns Spectrums. 13: 515-9. PMID 18567976 |
0.087 |
|
1987 |
Devine-Gage EA, Brown WT, Jenkins EC, Dutkowski R, Sammons D. Assignment of proteins to human chromosome 21 using two-dimensional gel electrophoresis and somatic cell genetics: An approach to the study of down syndrome Journal of Neurogenetics. 4: 215-226. PMID 2956403 DOI: 10.3109/01677068709102342 |
0.087 |
|
1985 |
Rudelli RD, Brown WT, Wisniewski K, Jenkins EC, Laure-Kamionowska M, Connell F, Wisniewski HM. Adult fragile X syndrome. Clinico-neuropathologic findings. Acta Neuropathologica. 67: 289-95. PMID 4050344 DOI: 10.1007/Bf00687814 |
0.087 |
|
2010 |
Kuizon S, DiMaiuta K, Walus M, Jenkins EC, Kuizon M, Kida E, Golabek AA, Espinoza DO, Pullarkat RK, Junaid MA. A critical tryptophan and Ca2+ in activation and catalysis of TPPI, the enzyme deficient in classic late-infantile neuronal ceroid lipofuscinosis. Plos One. 5: e11929. PMID 20689811 DOI: 10.1371/journal.pone.0011929 |
0.086 |
|
1991 |
Brooks SS, Cohen I, Ferrando C, Jenkins EC, Brown WT, Dobkin C. Cytogenetically negative, linkage positive 'fragile X' syndrome American Journal of Medical Genetics. 38: 370-373. PMID 1673313 DOI: 10.1002/ajmg.1320380242 |
0.085 |
|
1997 |
Jenkins EC, Schupf N, Genovese M, Ye LL, Kapell D, Canto B, Harris M, Devenny D, Lee JH, Brown WT. Increased low-level chromosome 21 mosaicism in older individuals with Down syndrome American Journal of Medical Genetics. 68: 147-151. PMID 9028448 DOI: 10.1002/(Sici)1096-8628(19970120)68:2<147::Aid-Ajmg5>3.0.Co;2-M |
0.085 |
|
2011 |
Cohen IL, Liu X, Lewis ME, Chudley A, Forster-Gibson C, Gonzalez M, Jenkins EC, Brown WT, Holden JJ. Autism severity is associated with child and maternal MAOA genotypes. Clinical Genetics. 79: 355-62. PMID 20573161 DOI: 10.1111/j.1399-0004.2010.01471.x |
0.085 |
|
1983 |
Jenkins EC, Duncan CJ, Wright CE, Giordano FM, Wilbur L, Wisniewski K, Sklower SL, French JH, Jones C, Brown WT. Atypical Down syndrome and partial trisomy 21. Clinical Genetics. 24: 97-102. PMID 6225574 |
0.084 |
|
1991 |
Jenkins EC, Sanz MM, Ray JH, Stark-Houck SL, Brown WT. Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villi American Journal of Medical Genetics. 38: 434-436. PMID 1826811 DOI: 10.1002/ajmg.1320380258 |
0.084 |
|
1997 |
Ceratto N, Dobkin C, Carter M, Jenkins E, Yao XL, Cassiman JJ, Aly MS, Bosco P, Leube R, Langbein L, Feo S, Romano V. Human type I cytokeratin genes are a compact cluster. Cytogenetics and Cell Genetics. 77: 169-74. PMID 9284906 DOI: 10.1159/000134566 |
0.084 |
|
1993 |
Brown WT, Houck GE, Jeziorowska A, Levinson FN, Ding X, Dobkin C, Zhong N, Henderson J, Brooks SS, Jenkins EC. Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test Jama: the Journal of the American Medical Association. 270: 1569-1575. PMID 8371467 DOI: 10.1001/jama.1993.03510130075034 |
0.084 |
|
1991 |
Jenkins LS, Gruenert DC, Jenkins EC, Schonberg SA. Transformation and establishment of fragile X cell lines from amniocytes American Journal of Medical Genetics. 38: 416-417. PMID 1850193 DOI: 10.1002/ajmg.1320380253 |
0.084 |
|
2001 |
Velinov M, Gu H, Shah K, Genovese M, Duncan C, Kupchik G, Jenkins EC. PCR-based methylation testing for Prader-Willi or Angelman syndromes using archived fixed-cell suspensions Genetic Testing. 5: 153-155. PMID 11551105 |
0.084 |
|
1979 |
Dutkowski RT, Kevin MJ, Jenkins EC. The effect of oral contraceptives on sister chromatid exchange and micronuclei formation Canadian Journal of Genetics and Cytology. 21: 560. |
0.083 |
|
1990 |
Jenkins EC, Duncan CJ, Sanz MM, Genovese M, Gu H, Schwartz-Richstein C, Lele KP, Salandi ML, Krawczun MS. Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures. Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology. 58: 236-40. PMID 2147548 DOI: 10.1159/000163591 |
0.083 |
|
2008 |
Jenkins EC, Tassone F, Ye L, Gu H, Xi M, Velinov M, Brown WT, Hagerman RJ, Hagerman PJ. Reduced telomere length in older men with premutation alleles of the fragile X mental retardation 1 gene. American Journal of Medical Genetics. Part A. 146: 1543-6. PMID 18478592 DOI: 10.1002/Ajmg.A.32342 |
0.083 |
|
2013 |
Gavin M, Wen GY, Messing J, Adelman S, Logush A, Jenkins EC, Brown WT, Velinov M. Substrate Reduction Therapy in Four Patients with Milder CLN1 Mutations and Juvenile-Onset Batten Disease Using Cysteamine Bitartrate. Jimd Reports. 11: 87-92. PMID 23588842 DOI: 10.1007/8904_2013_226 |
0.083 |
|
1992 |
Krawczun MS, Duncan CJ, Stark-Houck SL, Jenkins EC. Fra(X) prenatal diagnosis: Are endoreduplicated and polyploid cells useful diagnostic criteria? American Journal of Medical Genetics. 43: 149-154. PMID 1605184 DOI: 10.1002/ajmg.1320430123 |
0.083 |
|
1992 |
Jenkins EC, Brown WT, Schonberg S, Krawczun MS, Goldberg J, Golbus MS. Prenatal detection of fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in females American Journal of Medical Genetics. 43: 128-135. PMID 1605181 DOI: 10.1002/ajmg.1320430120 |
0.083 |
|
1988 |
Nolin SL, Jenkins EC, Brown WT, Dobkin CS. In situ nick translation of the fragile X region American Journal of Medical Genetics. 30: 443-450. PMID 3052067 |
0.082 |
|
1998 |
Ziemnicka-Kotula D, Xu J, Gu H, Potempska A, Kim KS, Jenkins EC, Trenkner E, Kotula L. Identification of a candidate human spectrin Src homology 3 domain- binding protein suggests a general mechanism of association of tyrosine kinases with the spectrin-based membrane skeleton Journal of Biological Chemistry. 273: 13681-13692. PMID 9593709 DOI: 10.1074/jbc.273.22.13681 |
0.082 |
|
2005 |
Zhong N, Ju W, Moroziewicz D, Wronska A, Li M, Wisniewski K, Brooks SS, Jenkins E, Brown WT. Prenatal diagnostic testing for infantile and late-infantile neuronal ceroid lipofusinoses (NCL) using allele specific primer extension (ASPE). Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences. 37: 20-5. PMID 15719035 |
0.081 |
|
2008 |
Jenkins EC, Ye L, Gu H, Ni SA, Duncan CJ, Velinov M, Pang D, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Increased "absence" of telomeres may indicate Alzheimer's disease/dementia status in older individuals with Down syndrome. Neuroscience Letters. 440: 340-3. PMID 18571319 DOI: 10.1016/J.Neulet.2008.05.098 |
0.081 |
|
1999 |
Dobkin C, Ding XH, Li SY, Houck G, Nolin SL, Glicksman A, Zhong N, Jenkins EC, Brown WT. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection American Journal of Medical Genetics. 83: 338-341. PMID 10208176 DOI: 10.1002/(SICI)1096-8628(19990402)83:4<338::AID-AJMG23>3.0.CO;2-3 |
0.081 |
|
1991 |
Krawczun MS, Jenkins EC, Duncan CJ, Stark-Houck SL, Kunaporn S, Schwatz-Richstein C, Gu H, Brown WT. Distribution of autosomal fragile sites in specimens cultured for prenatal fragile X diagnosis. American Journal of Medical Genetics. 38: 456-63. PMID 2018087 DOI: 10.1002/ajmg.1320380264 |
0.081 |
|
1977 |
Evans LA, Kevin MJ, Jenkins EC. Human sister chromatid exchange caused by methylazoxymethanol acetate. Mutation Research. 56: 51-8. PMID 593294 DOI: 10.1016/0027-5107(77)90241-X |
0.08 |
|
1976 |
Evans LA, Kevin M, Jenkins EC. PHA response, sister chromatid exchange and methylazoxymethanol acetate (MAMac) Excerpta Med. Amsterdam, I.C.S.. |
0.08 |
|
1986 |
Fisch GS, Cohen IL, Wolf EG, Brown WT, Jenkins EC, Gross A. Autism and the fragile X syndrome American Journal of Psychiatry. 143: 71-73. PMID 3455802 |
0.079 |
|
1989 |
Krawczun MS, Jenkins EC, Masia A, Kunaporn S, Stark SL, Duncan CJ, Sklower SL, Rudelli RD. Chromosomal abnormalities in amniotic fluid cell cultures: a comparison of apparent pseudomosaicism in Chang and RPMI-1640 media. Clinical Genetics. 35: 139-45. PMID 2721022 |
0.079 |
|
1985 |
Krawczun MS, Jenkins EC, Brown WT. Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations Human Genetics. 69: 209-211. PMID 4038969 DOI: 10.1007/BF00293026 |
0.079 |
|
2018 |
Quadros EV, Sequeira JM, Brown WT, Mevs C, Marchi E, Flory M, Jenkins EC, Velinov MT, Cohen IL. Folate receptor autoantibodies are prevalent in children diagnosed with autism spectrum disorder, their normal siblings and parents. Autism Research : Official Journal of the International Society For Autism Research. PMID 29394471 DOI: 10.1002/aur.1934 |
0.078 |
|
1992 |
Brown WT, Jenkins EC, Goonewardena P, Miezejeski C, Atkin J, Devys D. Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairment. American Journal of Medical Genetics. 43: 96-102. PMID 1605241 DOI: 10.1002/ajmg.1320430114 |
0.078 |
|
2008 |
Isaacs CE, Wen GY, Xu W, Jia JH, Rohan L, Corbo C, Di Maggio V, Jenkins EC, Hillier S. Epigallocatechin gallate inactivates clinical isolates of herpes simplex virus. Antimicrobial Agents and Chemotherapy. 52: 962-70. PMID 18195068 DOI: 10.1128/Aac.00825-07 |
0.078 |
|
1991 |
Jenkins EC, Krawczun MS, Stark-Houck SL, Duncan CJ, Kunaporn S, Gu H, Schwartz-Richstein C, Howard-Peebles PN, Gross A, Sherman SL. Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures. American Journal of Medical Genetics. 38: 447-52. PMID 1826813 DOI: 10.1002/ajmg.1320380262 |
0.077 |
|
1988 |
Jenkins EC, Brown WT, Krawczun MS, Duncan CJ, Lele KP, Cantu ES, Schonberg S, Golbus MS, Sekhon GS, Stark S. Recent experience in prenatal fra(X) detection. American Journal of Medical Genetics. 30: 329-36. PMID 2972205 |
0.077 |
|
1986 |
Robakis NK, Devine-Gage EA, Jenkins EC, Kascsak RJ, Brown WT, Krawczun MS, Silverman WP. Localization of a human gene homologous to the PrP gene on the p arm of chromosome 20 and detection of PrP-related antigens in normal human brain. Biochemical and Biophysical Research Communications. 140: 758-65. PMID 2877664 DOI: 10.1016/0006-291X(86)90796-5 |
0.077 |
|
2015 |
Jenkins EC, Ye L, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Telomere longitudinal shortening as a biomarker for dementia status of adults with Down syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26593971 DOI: 10.1002/Ajmg.B.32389 |
0.076 |
|
1988 |
Krawczun MS, Jenkins EC, Brown WT, Silverman WP. Fragile X expression in short-term whole blood cultures is affected by cell density American Journal of Medical Genetics. 30: 435-442. PMID 2972206 |
0.076 |
|
1986 |
Jenkins EC, Kastin BR, Krawczun MS, Lele KP, Silverman WP, Brown WT. Fragile X chromosome frequency is consistent temporally and within replicate cultures. American Journal of Medical Genetics. 23: 475-81. PMID 3953660 |
0.076 |
|
2017 |
Jenkins EC, Marchi EJ, Velinov MT, Ye L, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Longitudinal telomere shortening and early Alzheimer's disease progression in adults with down syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28856789 DOI: 10.1002/Ajmg.B.32575 |
0.076 |
|
2002 |
Jenkins EC, Wen GY, Jenkins EC, Genovese M, Brown WT. Human chromatid ultrastructure: new observations with scanning and transmission electron microscopy. Scanning. 24: 55-8. PMID 12004804 |
0.076 |
|
1987 |
Brown WT, Jenkins EC, Gross AC, Chan CB, Wisniewski K, Cohen IL, Miezejeski CM. Genetics and expression of the fragile X syndrome Upsala Journal of Medical Sciences, Supplement. 44: 137-154. PMID 2895523 |
0.076 |
|
1991 |
Cohen IL, Sudhalter V, Pfadt A, Jenkins EC, Brown WT, Vietze PM. Why are autism and the fragile-X syndrome associated? Conceptual and methodological issues American Journal of Human Genetics. 48: 195-202. PMID 1990832 |
0.075 |
|
1984 |
Jenkins EC, Brown WT, Brooks J, Duncan CJ, Rudelli RD, Wisniewski HM. Experience with prenatal fragile X detection American Journal of Medical Genetics. 17: 215-239. PMID 6711597 |
0.075 |
|
1976 |
Jenkins EC, Wilbur L, Giordano FM. Chromosomal abnormality and 1, 9, and 16qh variation in a mentally retarded population Excerpta Med.,Amsterdam,I.C.S.. |
0.074 |
|
1999 |
Jenkins EC, Wen GY, Kim KS, Zhong N, Sapienza VJ, Hong H, Chen J, Li SY, Houck GE, Ding X, Nolin SL, Dobkin CS, Brown WT. Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies. American Journal of Medical Genetics. 83: 342-6. PMID 10208177 DOI: 10.1002/(SICI)1096-8628(19990402)83:4<342::AID-AJMG24>3.0.CO;2-H |
0.074 |
|
1999 |
Allingham-Hawkins DJ, Babul-Hirji R, Chitayat D, Holden JJ, Yang KT, Lee C, Hudson R, Gorwill H, Nolin SL, Glicksman A, Jenkins EC, Brown WT, Howard-Peebles PN, Becchi C, Cummings E, et al. Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data. American Journal of Medical Genetics. 83: 322-5. PMID 10208170 DOI: 10.1002/(Sici)1096-8628(19990402)83:4<322::Aid-Ajmg17>3.0.Co;2-B |
0.074 |
|
2012 |
Jenkins EC, Ye L, Silverman WP. Does the cryogenic freezing process cause shorter telomeres? Cryobiology. 65: 72-3. PMID 22465657 DOI: 10.1016/j.cryobiol.2012.03.005 |
0.073 |
|
1991 |
Jenkins EC, Brooks SE, Stark-Houck SL, Duncan CJ, Brooks SL, Brown WT. SV40-transformed fragile (X) amniocytes. American Journal of Medical Genetics. 38: 464-6. PMID 1850194 DOI: 10.1002/ajmg.1320380265 |
0.073 |
|
2011 |
Guariglia SR, Jenkins EC, Chadman KK, Wen GY. Chlorination byproducts induce gender specific autistic-like behaviors in CD-1 mice. Neurotoxicology. 32: 545-53. PMID 21740927 DOI: 10.1016/J.Neuro.2011.06.008 |
0.073 |
|
1992 |
Jenkins EC, Duncan CJ, Gu H, Genovese M, Krawczun MS. Dialyzed fetal bovine serum increases cytogenetic fragile X expression American Journal of Medical Genetics. 43: 155-160. PMID 1534967 DOI: 10.1002/ajmg.1320430124 |
0.071 |
|
1992 |
Nolin SL, Snider DA, Jenkins EC, Dobkin CS, Patchell K, Krawczun M, Strong G, Colwell M, Victor A, Payyapilli T, Turczyn M, Little A, Nagaraja U, Doyle N, Kenefick B, et al. New York State screening program for fragile X syndrome: A progress report American Journal of Medical Genetics. 43: 328-332. PMID 1605206 DOI: 10.1002/ajmg.1320430150 |
0.071 |
|
1986 |
Jenkins EC, Brown WT, Wilson MG, Lin MS, Alfi OS, Wassman ER, Brooks J, Duncan CJ, Masia A, Krawczun MS. The prenatal detection of the fragile X chromosone: Review of recent experience American Journal of Medical Genetics. 23: 297-311. PMID 2937295 |
0.071 |
|
1987 |
Brown WT, Wu Y, Gross AC, Chan CB, Dobkin CS, Jenkins EC. RFLP for linkage analysis of fragile X syndrome Lancet. 1: 280. PMID 2880102 DOI: 10.1016/S0140-6736(87)90103-6 |
0.071 |
|
1981 |
Jenkins EC, Evans LA. In vitro human lymphocyte PHA response- the heterogeneous effect of methylazoxymethanol acetate. Experimental Cell Biology. 49: 118-24. PMID 7202796 |
0.07 |
|
1986 |
Jenkins EC, Duncan CJ, Krawczun MS, Berns LM, Sanz MM, Brown WT. Frequency of tri- or multiradial configurations in fragile X identification American Journal of Medical Genetics. 23: 531-535. PMID 2937304 |
0.07 |
|
1976 |
Jenkins EC, Chaganti RSK, Wilbur L, German J. Ambiguous genitalia and mental retardation associated with a translocation 46,XY,t(9;10) and a deletion in 9q Birth Defects: Original Article Series. 12: 169-173. PMID 953219 |
0.07 |
|
2000 |
Velinov M, Gu H, Genovese M, Duncan C, Brown WT, Jenkins E. The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA Molecular Genetics and Metabolism. 69: 81-83. PMID 10655162 DOI: 10.1006/mgme.1999.2941 |
0.069 |
|
1974 |
Jenkins EC, Janerich AD, Giordano FM. Short term human leucocyte culture micromethod versus the macromethod Cytologia. 39: 353-356. PMID 4434765 |
0.069 |
|
1992 |
Hinton VJ, Dobkin CS, Halperin JM, Jenkins EC, Brown WT, Ding XH, Cohen IL, Rousseau F, Miezejeski CM. Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndrome. American Journal of Medical Genetics. 43: 87-95. PMID 1605240 DOI: 10.1002/Ajmg.1320430113 |
0.069 |
|
1996 |
Brown WT, Nolin S, Houck G, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E. Prenatal diagnosis and carrier screening for fragile X by PCR American Journal of Medical Genetics. 64: 191-195. PMID 8826474 DOI: 10.1002/(SICI)1096-8628(19960712)64:1<191::AID-AJMG34>3.0.CO;2-G |
0.069 |
|
2017 |
Jenkins EC, Ye L, Marchi E, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. An improved method for detecting telomere size differences in T-lymphocyte interphases from older people with Down syndrome with and without mild cognitive impairment. Biology Methods & Protocols. 2: bpx005. PMID 32161788 DOI: 10.1093/Biomethods/Bpx005 |
0.069 |
|
1975 |
Jenkins EC, Curcuru Giordano FM, Krishna SG, Cantarella J. De novo occurrence of 46,XX,t(4;13) (q31;q14) in a mentally retarded girl Annales De Genetique. 18: 117-120. PMID 1081364 |
0.069 |
|
1977 |
Kardon NB, Salwen HR, Krauss MA, Davis JG, Jenkins EC. De novo trisomy 9pter→q13 Human Genetics. 38: 249. DOI: 10.1007/BF00527412 |
0.068 |
|
2014 |
Mazur-Kolecka B, Cohen IL, Gonzalez M, Jenkins EC, Kaczmarski W, Brown WT, Flory M, Frackowiak J. Autoantibodies against neuronal progenitors in sera from children with autism. Brain & Development. 36: 322-9. PMID 23838310 DOI: 10.1016/j.braindev.2013.04.015 |
0.068 |
|
1988 |
Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT. Constitutive fragile sites in fra(X) individuals. American Journal of Medical Genetics. 30: 429-34. PMID 3052066 |
0.068 |
|
1991 |
Brown WT, Gross A, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Detection of fragile X non-penetrant males by DNA marker analysis American Journal of Medical Genetics. 38: 292-297. PMID 1673300 DOI: 10.1002/ajmg.1320380226 |
0.067 |
|
1995 |
Wen GY, Mato A, Wisniewski HM, Malik MN, Jenkins EC, Sheikh AM, Kim KS. Light and electron microscopic immunocytochemical localization of two major proteins in garlic bulb. Journal of Cellular Biochemistry. 58: 481-9. PMID 7593270 DOI: 10.1002/Jcb.240580411 |
0.067 |
|
2006 |
Jenkins EC, Velinov MT, Ye L, Gu H, Li S, Jenkins EC, Brooks SS, Pang D, Devenny DA, Zigman WB, Schupf N, Silverman WP. Telomere shortening in T lymphocytes of older individuals with Down syndrome and dementia. Neurobiology of Aging. 27: 941-5. PMID 16046031 DOI: 10.1016/J.Neurobiolaging.2005.05.021 |
0.067 |
|
1984 |
Devine EA, Nolin SL, Houck GE, Jenkins EC, Miller DL, Brown WT. Isolation and regional localization by in situ hybridization of a unique gene segment to chromosome 21 Biochemical and Biophysical Research Communications. 121: 380-385. PMID 6732814 DOI: 10.1016/0006-291X(84)90733-2 |
0.066 |
|
1978 |
Jenkins EC, Salwen HR, Krauss MA. On trisomy 9pter→9q1 Birth Defects: Original Article Series. 14: 416. |
0.065 |
|
1972 |
Weed RG, Curcuru FM, Jenkins EC. The cryogenic preservation of human whole blood inoculum for short-term leucocyte chromosome microculture Cryobiology. 9: 273-276. PMID 4636203 DOI: 10.1016/0011-2240(72)90047-8 |
0.065 |
|
1989 |
Jenkins EC, Devine-Gage EA, Yao XL, Houck GE, Brown WT, Robakis NK, Wisniewski KE, Silverman WP, Reisberg B, Wisniewski HM. Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individuals. Progress in Clinical and Biological Research. 317: 269-75. PMID 2690102 DOI: 10.1097/00002093-198802030-00134 |
0.065 |
|
2002 |
Velinov M, Gu H, Yeboa K, Warburton D, Tubo T, Dhuper S, Lanter S, Delprino D, Kupchik G, Jenkins EC. Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation. American Journal of Medical Genetics. 107: 330-3. PMID 11840491 DOI: 10.1002/ajmg.10140 |
0.065 |
|
1983 |
Dutkowski RT, Kevin MJ, Jenkins EC. The effect of oral contraceptives on sister chromatid exchange, blast transformation, mitotic index and micronuclei formation Experimental Cell Biology. 51: 115-120. PMID 6840387 |
0.064 |
|
1999 |
Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. Ultrastructure of the fragile X chromosome: new observations on the fragile site. American Journal of Medical Genetics. 83: 331-3. PMID 10208174 DOI: 10.1002/(Sici)1096-8628(19990402)83:4<331::Aid-Ajmg21>3.0.Co;2-U |
0.064 |
|
1997 |
Wen GY, Jenkins EC, Yao XL, Yoon D, Brown WT, Wisniewski HM. Transmission electron microscopy of chromosomes by longitudinal section preparation: application to fragile X chromosome analysis. American Journal of Medical Genetics. 68: 445-9. PMID 9021019 DOI: 10.1002/(Sici)1096-8628(19970211)68:4<445::Aid-Ajmg14>3.0.Co;2-S |
0.064 |
|
1988 |
Fisch GS, Cohen IL, Jenkins EC, Brown WT. Screening developmentally disabled male populations for fragile X: The effect of sample size American Journal of Medical Genetics. 30: 655-663. PMID 3052070 |
0.064 |
|
1988 |
Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X American Journal of Medical Genetics. 30: 551-566. PMID 2902796 |
0.064 |
|
2010 |
Jenkins EC, Ye L, Gu H, Ni SA, Velinov M, Pang D, Krinsky-McHale SJ, Zigman WB, Schupf N, Silverman WP. Shorter telomeres may indicate dementia status in older individuals with Down syndrome. Neurobiology of Aging. 31: 765-71. PMID 18635289 DOI: 10.1016/J.Neurobiolaging.2008.06.001 |
0.064 |
|
1986 |
Miezejeski CM, Jenkins EC, Hill AL, Wisniewski K, French JH, Brown WT. A profile of cognitive deficit in females from fragile X families. Neuropsychologia. 24: 405-9. PMID 3736823 DOI: 10.1016/0028-3932(86)90026-6 |
0.063 |
|
1984 |
Sklower SL, Jenkins EC, Nolin SL, Duncan CJ, Warburton D, Yeboa KA, Merkrebs A, Schwartz R, Wisniewski K, Stimson C, Ted Brown W. Distal duplication 14q: Report of three cases and further delineation of the syndrome Human Genetics. 68: 159-164. PMID 6500567 DOI: 10.1007/BF00279307 |
0.063 |
|
1987 |
Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS. Further evidence for genetic heterogeneity in the fragile X syndrome Human Genetics. 75: 311-321. PMID 2883105 DOI: 10.1007/BF00284100 |
0.063 |
|
1992 |
Jeziorowska A, Houck GE, Yao XL, Sklower-Brooks SL, Wisniewski KE, Jenkins EC, Wisniewski HM. Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH). Clinical Genetics. 42: 124-8. PMID 1395083 |
0.062 |
|
1991 |
Brown WT, Gross AC, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8 American Journal of Medical Genetics. 38: 343-346. PMID 1673308 DOI: 10.1002/ajmg.1320380235 |
0.061 |
|
1994 |
Yao XL, Jenkins EC. Translocation 4p;21q identified by FISH in a case previously described as 'presumptive monosomy 21' [1] American Journal of Medical Genetics. 52: 491-492. PMID 7747765 |
0.061 |
|
1974 |
Sandstrom MM, Jenkins EC. Cytological elucidation of a 17p marker chromosome Caryologia. 27: 307-313. DOI: 10.1080/00087114.1974.10796583 |
0.061 |
|
1993 |
Jeziorowska A, Ciesla W, Houck GE, Yao XL, Harris MS, Truszczak B, Skorski M, Jakubowski L, Jenkins EC, Kaluzewski B. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3). American Journal of Medical Genetics. 46: 83-7. PMID 7684191 DOI: 10.1002/ajmg.1320460114 |
0.06 |
|
1985 |
Wisniewski KE, French JH, Fernando S, Brown WT, Jenkins EC, Friedman E, Hill AL, Miezejeski CM. Fragile X syndrome: associated neurological abnormalities and developmental disabilities. Annals of Neurology. 18: 665-9. PMID 4083849 DOI: 10.1002/ana.410180607 |
0.06 |
|
1980 |
Kardon NB, Berger AL, Elice M, Davis JG, Jenkins EC. A liveborn case of 49,XXXY, + 18. Journal of Medical Genetics. 17: 389-90. PMID 7194375 |
0.06 |
|
2006 |
Mazur‐Kolecka B, Cohen I, Jenkins E, Kaczmarski W, Flory M, Frackowiak J. [P87]: A new cell culture model to study alterations of early neuronal development in autism International Journal of Developmental Neuroscience. 24: 533-533. DOI: 10.1016/j.ijdevneu.2006.09.150 |
0.06 |
|
1988 |
Jenkins EC, Devine-Gage EA, Robakis NK, Yao XL, Brown WT, Houck GE, Wolfe G, Ramakrishna N, Silverman WP, Wisniewski HM. Fine mapping of an Alzheimer disease-associated gene encoding beta-amyloid protein. Biochemical and Biophysical Research Communications. 151: 1-8. PMID 3279948 DOI: 10.1016/0006-291X(88)90551-7 |
0.06 |
|
1986 |
Krawczun MS, Lele KP, Jenkins EC, Brown WT. Fragile X expression increased by low cell-culture density. American Journal of Medical Genetics. 23: 467-73. PMID 2937301 |
0.059 |
|
2017 |
Park E, Cohen I, Gonzalez M, Castellano MR, Flory M, Jenkins EC, Brown WT, Schuller-Levis G. Is Taurine a Biomarker in Autistic Spectrum Disorder? Advances in Experimental Medicine and Biology. 975: 3-16. PMID 28849439 DOI: 10.1007/978-94-024-1079-2_1 |
0.059 |
|
1990 |
Krawczun MS, Jenkins EC, Lele KP, Sersen EA, Wisniewski HM. Study of spindle microtubule reassembly in cells from Alzheimer and Down syndrome patients following exposure to colcemid. Alzheimer Disease and Associated Disorders. 4: 203-16. PMID 2148262 DOI: 10.1097/00002093-199040400-00002 |
0.058 |
|
1994 |
Jenkins EC, Genovese M, Duncan CJ, Gu H, Stark-Houck S, Li - SY, Henderson J, Morys I, Brown WT. Occurrence of aneuploidy for the X chromosome in over 1,300 unrelated specimens screened for the fragile X chromosome [4] American Journal of Medical Genetics. 51: 452-453. PMID 7943017 DOI: 10.1002/ajmg.1320510430 |
0.058 |
|
2011 |
Liu X, Solehdin F, Cohen IL, Gonzalez MG, Jenkins EC, Lewis ME, Holden JJ. Population- and family-based studies associate the MTHFR gene with idiopathic autism in simplex families. Journal of Autism and Developmental Disorders. 41: 938-44. PMID 21069446 DOI: 10.1007/s10803-010-1120-x |
0.057 |
|
1983 |
Silverman W, Lubin R, Jenkins EC, Brown WT. The strength of association between fragile (X) chromosome presence and mental retardation Clinical Genetics. 23: 436-440. PMID 6684008 |
0.057 |
|
2015 |
Wang L, Meng Q, Tang X, Yin T, Zhang J, Yang S, Wang X, Wu H, Shi Q, Jenkins EC, Zhong N, Gu Y. Maternal mosaicism of sex chromosome causes discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing. Taiwanese Journal of Obstetrics & Gynecology. 54: 527-31. PMID 26522104 DOI: 10.1016/j.tjog.2014.10.009 |
0.056 |
|
2015 |
Schupf N, Lee A, Park N, Dang LH, Pang D, Yale A, Oh DK, Krinsky-McHale SJ, Jenkins EC, Luchsinger JA, Zigman WB, Silverman W, Tycko B, Kisselev S, Clark L, et al. Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome. Neurobiology of Aging. PMID 26166206 DOI: 10.1016/J.Neurobiolaging.2015.06.020 |
0.055 |
|
1986 |
Brown WT, Jenkins EC, Cohen IL, Fisch GS, Wolf-Schein EG, Gross A, Waterhouse L, Fein D, Mason-Brothers A, Ritvo E. Fragile X and autism: a multicenter survey. American Journal of Medical Genetics. 23: 341-52. PMID 3513570 |
0.055 |
|
1984 |
Brown WT, Jenkins EC, Friedman E, Brooks J, Cohen IL, Duncan C, Hill AL, Malik MN, Morris V, Wolf E. Folic acid therapy in the fragile X syndrome. American Journal of Medical Genetics. 17: 289-97. PMID 6711601 DOI: 10.1002/ajmg.1320170121 |
0.055 |
|
1991 |
Nolin SL, Snider DA, Jenkins EC, Brown WT, Krawczun M, Stetka D, Houck G, Dobkin CS, Strong G, Smith-Dobransky G, Victor A, Hughes K, Kimpton D, Little A, Nagaraja U, et al. Fragile X screening program in New York state American Journal of Medical Genetics. 38: 251-255. PMID 2018068 DOI: 10.1002/ajmg.1320380218 |
0.055 |
|
1977 |
Kardon NB, Krauss M, Davis JG, Jenkins EC, Island S. Chromosomal mosaicism in amniotic fluid cell cultures The Journal of Pediatrics. 90: 501-502. PMID 839359 DOI: 10.1016/S0022-3476(77)80745-2 |
0.055 |
|
1977 |
Wilbur L, Curcuru-Giordano FM, Krishna SG, Kardon NB, Jenkins EC. A case of 46,XY,t(1;13) (q24;q32) with mental retardation Human Genetics. 37: 239-242. PMID 885541 DOI: 10.1007/BF00393588 |
0.054 |
|
2008 |
Zigman WB, Devenny DA, Krinsky-McHale SJ, Jenkins EC, Urv TK, Wegiel J, Schupf N, Silverman W. Alzheimer's Disease in Adults with Down Syndrome. International Review of Research in Mental Retardation. 36: 103-145. PMID 19633729 DOI: 10.1016/S0074-7750(08)00004-9 |
0.053 |
|
2003 |
Wen GY, Fisher MB, Genovese M, Goldberg EM, Jenkins EC. Brush-like fibers on the human chromosome periphery. Scanning. 25: 316-20. PMID 14696981 |
0.051 |
|
1985 |
Brown WT, Gross AC, Chan CB, Jenkins EC. Genetic linkage heterogeneity in the fragile X syndrome Human Genetics. 71: 11-18. PMID 2993154 DOI: 10.1007/BF00295659 |
0.051 |
|
2005 |
Zigman WB, Jenkins EC, Tycko B, Schupf N, Silverman W. Mortality is associated with apolipoprotein E epsilon4 in nondemented adults with Down syndrome. Neuroscience Letters. 390: 93-7. PMID 16122874 DOI: 10.1016/J.Neulet.2005.08.002 |
0.05 |
|
1976 |
Weed RG, Jenkins EC. Dimethyl sulphoxide (DMSO) and glycerol in the cryogenic preservation of peripheral blood for phytohemagglutinin (PHA) induced short term microcultures Cryobiology. 13: 655. |
0.05 |
|
1991 |
Brown WT, Jenkins E, Neri G, Lubs H, Shapiro LR, Davies KE, Sherman S, Hagerman R, Laird C. Conference report: Fourth International Workshop on the fragile X and X-linked mental retardation. American Journal of Medical Genetics. 38: 158-72. PMID 1673296 DOI: 10.1002/ajmg.1320380202 |
0.049 |
|
1975 |
Evans LA, Jenkins EC. Methylazoxymethanol and PHA responses in human short term leukocyte cultures Mutation Research. 31: 319-320. |
0.049 |
|
1988 |
Wolf-Schein EG, Jenkins EC, Sklower S, Cohen IL, Wisniewski KE, Brown WT. On the association of fragile X with autism. Journal of Autism and Developmental Disorders. 18: 457-8. PMID 3170461 DOI: 10.1007/Bf02212200 |
0.048 |
|
1989 |
Cohen IL, Brown WT, Jenkins EC, Krawczun MS, French JH, Raguthu S, Wolf-Schein EG, Sudhalter V, Fisch G, Wisniewski K. Fragile X syndrome in females with autism American Journal of Medical Genetics. 34: 302-303. PMID 2817015 |
0.048 |
|
1989 |
Reisberg B, Ferris SH, Franssen E, Jenkins EC, Wisniewski KE. Clinical features of a neuropathologically verified familial Alzheimer's cohort with onset in the fourth decade: comparison with senile onset Alzheimer's disease and etiopathogenic implications. Progress in Clinical and Biological Research. 317: 43-54. PMID 2690108 |
0.047 |
|
1986 |
Brown WT, Gross AC, Chan CB, Jenkins EC. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity American Journal of Medical Genetics. 23: 643-664. PMID 3006490 |
0.047 |
|
1982 |
Evans LA, Duncan CJ, Jenkins EC. The type of chromosomal damage caused by methylazoxymethanol acetate. A comparison between chromosome breakage and SCE. Cytologia. 47: 683-7. PMID 7166056 |
0.047 |
|
1997 |
Miezejeski CM, Heaney G, Belser R, Brown WT, Jenkins EC, Sersen EA. Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation American Journal of Medical Genetics - Neuropsychiatric Genetics. 74: 167-171. PMID 9129717 DOI: 10.1002/(SICI)1096-8628(19970418)74:2<167::AID-AJMG10>3.0.CO;2-G |
0.047 |
|
1991 |
Brown WT, Goonewardena P, Gross AC, Dobkin C, Jenkins EC. Molecular markers of fragile X: application to males at risk in fragile X families Progress in Clinical and Biological Research. 368: 73-77. PMID 1946507 |
0.046 |
|
1992 |
Jenkins EC. In memoriam: Michael S. Krawczun, Ph.D., D.A.B.M.G. [1952-1991] American Journal of Medical Genetics. 43: 3-4. DOI: 10.1002/ajmg.1320430103 |
0.046 |
|
1982 |
Brown WT, Jenkins EC, Friedman E, Brooks J, Wisniewski K, Raguthu S, French J. Autism is associated with the fragile-X syndrome Journal of Autism and Developmental Disorders. 12: 303-308. PMID 7153204 DOI: 10.1007/BF01531375 |
0.046 |
|
1982 |
Brown WT, Friedman E, Jenkins EC, Brooks J, Wisniewski K, Raguthu S, French JH. ASSOCIATION OF FRAGILE X SYNDROME WITH AUTISM The Lancet. 319: 100. PMID 6119460 DOI: 10.1016/S0140-6736(82)90231-8 |
0.046 |
|
1991 |
Cohen IL, Vietze PM, Sudhalter V, Jenkins EC, Brown WT. Effects of age and communication level on eye contact in fragile X males and non-fragile X autistic males American Journal of Medical Genetics. 38: 498-502. PMID 2018093 DOI: 10.1002/ajmg.1320380271 |
0.046 |
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1973 |
Sandstrom MM, Jenkins EC. A 17p marker chromosome familial study. Annales De Gã©Nã©Tique. 16: 267-9. PMID 4544091 |
0.045 |
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1988 |
Brown WT, Gross A, Chan C, Jenkins EC, Mandel JL, Oberlé I, Arveiler B, Novelli G, Thibodeau S, Hagerman R, Summers K, Turner G, White BN, Mulligan L, Forster-Gibson C, et al. Multilocus analysis of the fragile X syndrome Human Genetics. 78: 201-205. PMID 3162224 DOI: 10.1007/Bf00291662 |
0.044 |
|
1988 |
Fisch GS, Cohen IL, Gross AC, Jenkins V, Jenkins EC, Brown WT. Folic acid treatment of fragile X males: A further study American Journal of Medical Genetics. 30: 393-399. PMID 3052065 |
0.044 |
|
1999 |
Holden JJ, Percy M, Allingham-Hawkins D, Brown WT, Chiurazzi P, Fisch G, Gane L, Gunter C, Hagerman R, Jenkins EC, Kooy RF, Lubs HA, Murray A, Neri G, Schwartz C, et al. Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997. American Journal of Medical Genetics. 83: 221-36. PMID 10208154 DOI: 10.1002/(Sici)1096-8628(19990402)83:4<221::Aid-Ajmg1>3.0.Co;2-K |
0.044 |
|
2001 |
Jenkins E, Upton W. Internally Generated Intangible Assets: Framing the Discussion Australian Accounting Review. 11: 4-11. DOI: 10.1111/j.1835-2561.2001.tb00183.x |
0.043 |
|
1999 |
Zhong N, Ju W, Brown WT, Ye L, Jenkins EC, Schupf N. Distribution of apolipoprotein E genotypes in fragile X syndrome and batten disease [7] American Journal of Medical Genetics. 84: 309-310. PMID 10331615 DOI: 10.1002/(SICI)1096-8628(19990528)84:3<309::AID-AJMG30>3.0.CO;2-Z |
0.043 |
|
1983 |
Wisneiwski K, Dambska M, Jenkins EC. Monosomy 21 syndromes: further delineation including clinical, neuropathological, cytogenetic and biochemical studies Clinical Genetics. 23: 102-110. PMID 6839521 |
0.043 |
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1998 |
Jenkins EC, Ye L, Gu H, Wisniewski HM. Mitotic index and Alzheimer's disease. Neuroreport. 9: 3857-61. PMID 9875718 DOI: 10.1097/00001756-199812010-00017 |
0.043 |
|
1992 |
Mandel JL, Hagerman R, Froster U, Brown WT, Jenkins EC, Jacobs P, Turner G, Lubs H, Neri G. Fifth International Workshop on the Fragile X and X-Linked Mental Retardation American Journal of Medical Genetics. 43: 5-27. PMID 1605233 DOI: 10.1002/ajmg.1320430104 |
0.043 |
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1985 |
Brown WT, Devine EA, Nolin SL, Houck GE, Jenkins EC. Localization of chromosome 21 probes by in situ hybridization. Annals of the New York Academy of Sciences. 450: 69-83. PMID 3160293 DOI: 10.1111/j.1749-6632.1985.tb21484.x |
0.042 |
|
1991 |
Jenkins EC, Krawczun MS, Brooks SE, Brooks SL, Sherman SL, Brown WT. Laboratory aspects of prenatal fra(X) detection Progress in Clinical and Biological Research. 368: 27-42. PMID 1835094 |
0.042 |
|
1970 |
Jenkins EC. Phenothiazines and chromosome damage Cytologia. 35: 552-560. PMID 5533360 |
0.042 |
|
1971 |
Jenkins EC, Weed RG. An analysis of several slide preparation techniques for human peripheral blood cultures Acta Geneticae Medicae Et Gemellologiae. 20: 85-95. PMID 5568115 |
0.041 |
|
1999 |
Wen GY, Jenkins EC, Goldberg EM, Genovese M, Brown WT, Wisniewski HM. First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends. American Journal of Medical Genetics. 83: 334-7. PMID 10208175 DOI: 10.1002/(Sici)1096-8628(19990402)83:4<334::Aid-Ajmg22>3.0.Co;2-I |
0.041 |
|
2001 |
Jenkins EC, Wen GY, Genovese M, Brown WT. New observations of human chromosome scanning electron microscopy and transmission electron microscopy Scanning. 23: 143-144. |
0.041 |
|
1984 |
Miezejeski CM, Jenkins EC, Hill AL, Wisniewski K, Brown WT. Verbal vs. nonverbal ability, fragile X syndrome, and heterozygous carriers. American Journal of Human Genetics. 36: 227-9. PMID 6695921 |
0.04 |
|
1972 |
Jenkins EC. Wire-loop application of liquid emulsion to slides for autoradiography in light microscopy Biotechnic and Histochemistry. 47: 23-26. DOI: 10.3109/10520297209116530 |
0.04 |
|
1999 |
Madahar CJ, Jenkins E, Coomaralingam R, Roy J, Yanza A. Congenital cardiac myopathy in a baby with an apparently balanced translocation t(7;8)(p21.2;g24.1) Genetics in Medicine. 1: 69-69. DOI: 10.1097/00125817-199901000-00109 |
0.04 |
|
2007 |
Zigman WB, Schupf N, Jenkins EC, Urv TK, Tycko B, Silverman W. Cholesterol level, statin use and Alzheimer's disease in adults with Down syndrome. Neuroscience Letters. 416: 279-84. PMID 17353095 DOI: 10.1016/J.Neulet.2007.02.023 |
0.039 |
|
1986 |
Brown WT, Cohen IL, Fisch GS, Wolf-Schein EG, Jenkins VA, Malik MN, Jenkins EC. High dose folic acid treatment of fragile (X) males American Journal of Medical Genetics. 23: 263-271. PMID 3513568 |
0.039 |
|
1988 |
Cohen IL, Fisch GS, Sudhalter V, Wolf-Schein G, Hanson D, Hagerman R, Jenkins EC, Brown WT. Social gaze, social avoidance, and repetitive behavior in fragile X males: A controlled study American Journal On Mental Retardation. 92: 436-446. PMID 2965890 |
0.039 |
|
1986 |
Sanz MM, Jenkins EC, Brown WT, Davisson MT, Kevin MJ, Roderick TH, Silverman WP, Wisniewski HM. Mouse chromosome fragility. American Journal of Medical Genetics. 23: 491-509. PMID 2937303 DOI: 10.1002/Ajmg.1320230141 |
0.038 |
|
1973 |
Jenkins EC, Sandstrom MM. C-mitosis without colchicine in human leucocyte cultures. Cytologia. 38: 159-63. PMID 4581602 |
0.037 |
|
2007 |
Jenkins EC, Ye L, Gu H, Ni SA, Velinov M, Pang D, Devenny DA, Zigman WB, Schupf N, Silverman WP. P-039: Telomere shortening and/or “absence” may indicate dementia/AD status in older individuals with down syndrome Alzheimer's & Dementia. 3: S109-S110. DOI: 10.1016/J.Jalz.2007.04.255 |
0.037 |
|
1999 |
Velinov M, Zhong N, Brown WT, Jenkins E. PCR-based molecular diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite treatment. Potential for quantitative estimation Genetics in Medicine. 1: 75-75. DOI: 10.1097/00125817-199901000-00135 |
0.036 |
|
1992 |
Brown WT, Jenkins EC. The fragile X syndrome Molecular Genetic Medicine. 2: 39-66. PMID 1458226 DOI: 10.1016/B978-0-12-462002-5.50007-8 |
0.036 |
|
1986 |
Brown WT, Jenkins EC, Krawczun MS, Wisniewski K, Rudelli R, Cohen IL, Fisch G, Wolf-Schein E, Miezejeski C, Dobkin C. The fragile X syndrome Annals of the New York Academy of Sciences. 477: 129-150. PMID 3545014 DOI: 10.1111/j.1749-6632.1986.tb40329.x |
0.036 |
|
1981 |
Brown WT, Mezzacappa PM, Jenkins EC. Screening for fragile X syndrome by testicular size measurement Lancet. 2: 1055. PMID 6118515 |
0.036 |
|
2008 |
Krinsky-McHale SJ, Devenny DA, Gu H, Jenkins EC, Kittler P, Murty VV, Schupf N, Scotto L, Tycko B, Urv TK, Ye L, Zigman WB, Silverman W. Successful aging in a 70-year-old man with down syndrome: a case study. Intellectual and Developmental Disabilities. 46: 215-28. PMID 18578579 DOI: 10.1352/2008.46:215-228 |
0.035 |
|
1989 |
Cohen IL, Vietze PM, Sudhalter V, Jenkins EC, Brown WT. Parent-child dyadic gaze pattern in fragile X males and in non-fragile X males with autistic disorder Journal of Child Psychology and Psychiatry and Allied Disciplines. 30: 845-856. PMID 2592468 DOI: 10.1111/j.1469-7610.1989.tb00286.x |
0.034 |
|
1974 |
Curcuru Giordano FM, Weed RG, Jenkins EC. Banding analysis of the chromosomes of Marmosa mitis (murine opossum) Canadian Journal of Genetics and Cytology. 16: 31-38. PMID 4135053 |
0.033 |
|
2005 |
Krinsky-McHale SJ, Kittler P, Brown WT, Jenkins EC, Devenny DA. Repetition priming in adults with Williams syndrome: age-related dissociation between implicit and explicit memory. American Journal of Mental Retardation : Ajmr. 110: 482-96. PMID 16212450 DOI: 10.1352/0895-8017(2005)110[482:RPIAWW]2.0.CO;2 |
0.033 |
|
2004 |
Jenkins EC, Velinov M, Li S, Ye L, Jenkins EC, Gu H, Zigman WB, Schupf N, Brooks SS, Pang D, Silverman WP. P3-010 Telomere shortening and dementia in older individuals with down syndrome Neurobiology of Aging. 25: S354. DOI: 10.1016/S0197-4580(04)81165-5 |
0.033 |
|
2012 |
Krinsky-McHale SJ, Jenkins EC, Zigman WB, Silverman W. Ophthalmic disorders in adults with down syndrome. Current Gerontology and Geriatrics Research. 2012: 974253. PMID 22570648 DOI: 10.1155/2012/974253 |
0.032 |
|
1988 |
Schwartz CE, Phelan MC, Brightharp C, Pancoast I, Howard-Peebles PN, Thibodeau S, Brown WT, Jenkins EC. Fragile X syndrome: Linkage analysis in black and white populations American Journal of Medical Genetics. 30: 531-542. PMID 3177470 |
0.031 |
|
1974 |
Jenkins EC, Weed RG, Sandstrom MM. An additional case of partial trisomy 18. Annales De Gã©Nã©Tique. 17: 45-8. PMID 4546345 |
0.031 |
|
2004 |
Devenny DA, Krinsky-McHale SJ, Kittler PM, Flory M, Jenkins E, Brown WT. Age-associated memory changes in adults with williams syndrome. Developmental Neuropsychology. 26: 691-706. PMID 15525565 DOI: 10.1207/s15326942dn2603_3 |
0.031 |
|
1979 |
Weed RG, Jenkins EC. Slow versus fast postthaw dilution for the recovery of lymphocytes in whole blood frozen in either dimethyl sulfoxide or glycerol Experimental Cell Biology. 47: 351-359. PMID 527752 |
0.031 |
|
2000 |
Zhong NA, Wisniewski KE, Ju W, Moroziewicz DN, Jurkiewicz A, McLendon L, Jenkins EC, Brown WT. Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses. Genetic Testing. 4: 243-8. PMID 11142754 DOI: 10.1089/10906570050501452 |
0.03 |
|
1982 |
Brown WT, Jenkins EC. Fragile X: its detectability Hospital Practice (Office Ed.). 17. PMID 6809565 |
0.028 |
|
2004 |
Jenkins EC, Ye L, Li S, Zigman WB, Schupf N, Sersen EA, Zhong N, Miezejeski CM, Brooks SS, Silverman WP. Mitotic index in Down's syndrome with and without dementia. American Journal of Medical Genetics. Part A. 125: 315-7. PMID 14994244 DOI: 10.1002/Ajmg.A.20453 |
0.028 |
|
1992 |
Miezejeski C, Heaney G, Sersen E, Krawczun M, Jenkins E, Brown W. Brainstem auditory evoked responses in males with fragile X syndrome: Laterality and sedation effects Archives of Clinical Neuropsychology. 7: 349-350. DOI: 10.1093/arclin/7.4.349a |
0.025 |
|
1972 |
Jenkins EC. Waldenstrom's macroglobulinaemia and phytohaemagglutinin response. Lancet (London, England). 2: 437. PMID 4115263 DOI: 10.1016/S0140-6736(72)91843-0 |
0.023 |
|
1977 |
Jenkins EC, Weed RG. Slow and fast postthaw dilution in the cryoprotection of lymphocytes in whole blood Cryobiology. 14: 696-697. DOI: 10.1016/0011-2240(77)90067-0 |
0.022 |
|
1985 |
Brown WT, Kieras FJ, Houck GE, Dutkowski R, Jenkins EC. A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome Advances in Experimental Medicine and Biology. 190: 229-244. PMID 3909767 DOI: 10.1007/978-1-4684-7853-2_10 |
0.021 |
|
2003 |
Velinov M, Jenkins EC. PCR-based strategies for the diagnosis of Prader-Willi/Angelman syndromes. Methods in Molecular Biology (Clifton, N.J.). 217: 209-16. PMID 12491935 |
0.019 |
|
1976 |
Davis JG, Jenkins EC, Klinger HP, Weed RG. A child with presumptive monosomy 21 (45,XY,-21) in a family in which some members are Gq-. Cytogenetics and Cell Genetics. 17: 65-77. PMID 975937 |
0.018 |
|
2017 |
Krinsky-McHale SJ, Jenkins EC, Lee JH, Schupf N, Zigman WB, Silverman W. [P3-434]: INDIVIDUAL DIFFERENCES IN LIFELONG ABILITIES MUST BE CONSIDERED FOR STAGING OF EARLY AD Alzheimer's & Dementia. 13: P1134-P1135. DOI: 10.1016/J.Jalz.2017.06.1652 |
0.015 |
|
1971 |
Jenkins EC. A screening technique for the Lesch-Nyhan syndrome The Journal of Pediatrics. 79: 663-666. PMID 5094259 DOI: 10.1016/S0022-3476(71)80317-7 |
0.015 |
|
2007 |
Zigman WB, Schupf N, Jenkins EC, Urv TK, Tycko B, Silverman W. O2-04-01: Risk for Alzheimer's disease in down syndrome is related to cholesterol level and statin use Alzheimer's & Dementia. 3: S192-S192. DOI: 10.1016/J.Jalz.2007.04.296 |
0.014 |
|
1975 |
Jervis GA, Jenkins EC. Case report 31 Syndrome Identification. 3: 18-21. |
0.013 |
|
1988 |
BROWN WT, DEVINE-GAGE EA, JENKINS EC. GENETICS OF FAMILIAL ALZHEIMER DISEASE Alzheimer Disease & Associated Disorders. 2: 273. DOI: 10.1097/00002093-198802030-00122 |
0.012 |
|
2015 |
Farmer TD, Jenkins EC, O'Brien TP, McCoy GA, Havlik AE, Nass ER, Nicholson WE, Printz RL, Shiota M. Comparison of the physiological relevance of systemic vs. portal insulin delivery to evaluate whole body glucose flux during an insulin clamp. American Journal of Physiology. Endocrinology and Metabolism. 308: E206-22. PMID 25516552 DOI: 10.1152/ajpendo.00406.2014 |
0.01 |
|
1989 |
Wisniewski HM, Jenkins EC. In memoriam George A. Jervis, M.D., (August 15, 1903-June 5, 1986). Journal of Neuropathology and Experimental Neurology. 48: 109-10. PMID 2642298 |
0.01 |
|
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