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Edmund C. Jenkins, Ph.D. - Publications

Affiliations: 
2013 Biology City University of New York, New York, NY, United States 
Area:
General Biology, Human Development, Biochemistry
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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
1973 Sandstrom MM, Jenkins EC. A 17p marker chromosome familial study. Annales De Gã©Nã©Tique. 16: 267-9. PMID 4544091  0.045
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
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
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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