| Year |
Citation |
Score |
| 2021 |
Torres R, Fisher M, Birznieks G, Polymeropoulos C, Kay GG, Xiao C, Polymeropoulos MH. Simulated driving performance in healthy adults after night-time administration of 20 mg tasimelteon. Journal of Sleep Research. e13430. PMID 34152055 DOI: 10.1111/jsr.13430 |
0.68 |
|
| 2019 |
Smieszek S, Polymeropoulos C, Birznieks G, Polymeropoulos M. Large whole genome sequencing study identifies novel variants associated with intrinsic circadian period in humans Sleep Medicine. 64: S356. DOI: 10.1016/J.Sleep.2019.11.993 |
0.316 |
|
| 2019 |
Smieszek S, Torres R, Xiao D, Polymeropoulos C, Birznieks G, Polymeropoulos M. M86 Novel Mutation In Ppef2 Reported In A Family Affected With Schizophrenia: Whole Genome Sequencing Study European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.08.186 |
0.303 |
|
| 2015 |
Lockley SW, Dressman MA, Licamele L, Xiao C, Fisher DM, Flynn-Evans EE, Hull JT, Torres R, Lavedan C, Polymeropoulos MH. Tasimelteon for non-24-hour sleep-wake disorder in totally blind people (SET and RESET): two multicentre, randomised, double-masked, placebo-controlled phase 3 trials. Lancet (London, England). 386: 1754-64. PMID 26466871 DOI: 10.1016/S0140-6736(15)60031-9 |
0.701 |
|
| 2015 |
Lockley S, Dressman M, Changfu X, Fisher D, Torres R, Lavedan C, Licamele L, Polymeropoulos M. Le tasimelteon entraîne l’horloge circadienne et procure une amélioration significative aux personnes totalement aveugles, souffrant du libre-cours MéDecine Du Sommeil. 12: 55-56. DOI: 10.1016/J.Msom.2015.01.099 |
0.685 |
|
| 2009 |
Volpi S, Heaton C, Mack K, Hamilton JB, Lannan R, Wolfgang CD, Licamele L, Polymeropoulos MH, Lavedan C. Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. Molecular Psychiatry. 14: 1024-31. PMID 18521091 DOI: 10.1038/Mp.2008.52 |
0.311 |
|
| 2009 |
Lavedan C, Licamele L, Volpi S, Hamilton J, Heaton C, Mack K, Lannan R, Thompson A, Wolfgang CD, Polymeropoulos MH. Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study. Molecular Psychiatry. 14: 804-19. PMID 18521090 DOI: 10.1038/Mp.2008.56 |
0.409 |
|
| 2004 |
Lavedan C, Birznieks G, Dressman M, McCullough K, Paczkowski R, Torres R, Wolfgang C, Polymeropoulos M. Translating the Genome into individualized therapeutics Drug Development Research. 62: 371-382. DOI: 10.1002/Ddr.10390 |
0.71 |
|
| 2002 |
Lavedan C, Buchholtz S, Nussbaum RL, Albin RL, Polymeropoulos MH. A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration. Neuroscience Letters. 322: 57-61. PMID 11958843 DOI: 10.1016/S0304-3940(01)02513-7 |
0.313 |
|
| 2001 |
Teive HA, Raskin S, Iwamoto FM, Germiniani FM, Baran MH, Werneck LC, Allan N, Quagliato E, Leroy E, Ide SE, Polymeropoulos MH. The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease. Arquivos De Neuro-Psiquiatria. 59: 722-4. PMID 11593272 DOI: 10.1590/S0004-282X2001000500013 |
0.725 |
|
| 2001 |
Papapetropoulos S, Paschalis C, Athanassiadou A, Papadimitriou A, Ellul J, Polymeropoulos MH, Papapetropoulos T. Clinical phenotype in patients with alpha-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 70: 662-5. PMID 11309462 DOI: 10.1136/Jnnp.70.5.662 |
0.302 |
|
| 2001 |
Torres R, Leroy E, Hu X, Katrivanou A, Gourzis P, Papachatzopoulou A, Athanassiadou A, Beratis S, Collier D, Polymeropoulos MH. Mutation screening of the Wolfram syndrome gene in psychiatric patients. Molecular Psychiatry. 6: 39-43. PMID 11244483 DOI: 10.1038/Sj.Mp.4000787 |
0.749 |
|
| 2001 |
Touchman JW, Dehejia A, Chiba-Falek O, Cabin DE, Schwartz JR, Orrison BM, Polymeropoulos MH, Nussbaum RL. Human and Mouse α-Synuclein Genes: Comparative Genomic Sequence Analysis and Identification of a Novel Gene Regulatory Element Genome Research. 11: 78-86. PMID 11156617 DOI: 10.1101/Gr.165801 |
0.393 |
|
| 2000 |
Wintermeyer P, Krüger R, Kuhn W, Müller T, Woitalla D, Berg D, Becker G, Leroy E, Polymeropoulos M, Berger K, Przuntek H, Schöls L, Epplen JT, Riess O. Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients. Neuroreport. 11: 2079-2082. PMID 10923647 DOI: 10.1097/00001756-200007140-00004 |
0.403 |
|
| 2000 |
Ruiz-Perez VL, Ide SE, Strom TM, Lorenz B, Wilson D, Woods K, King L, Francomano C, Freisinger P, Spranger S, Marino B, Dallapiccola B, Wright M, Meitinger T, Polymeropoulos MH, et al. Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis. Nature Genetics. 24: 283-6. PMID 10700184 DOI: 10.1038/73508 |
0.755 |
|
| 1999 |
Torres R, Ide SE, Dehejia A, Baras A, Polymeropoulos MH. Genomic structure and localization of the human protein phosphatase 2A BRgamma regulatory subunit. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 6: 323-7. PMID 10574460 DOI: 10.1093/Dnares/6.5.323 |
0.784 |
|
| 1999 |
Hardy C, Khanim F, Torres R, Scott-Brown M, Seller A, Poulton J, Collier D, Kirk J, Polymeropoulos M, Latif F, Barrett T. Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1. American Journal of Human Genetics. 65: 1279-90. PMID 10521293 DOI: 10.1086/302609 |
0.748 |
|
| 1999 |
Athanassiadou A, Voutsinas G, Psiouri L, Leroy E, Polymeropoulos MH, Ilias A, Maniatis GM, Papapetropoulos T. Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synuclein. American Journal of Human Genetics. 65: 555-558. PMID 10417297 DOI: 10.1086/302486 |
0.322 |
|
| 1998 |
Lavedan C, Buchholtz S, Auburger G, Albin RL, Athanassiadou A, Blancato J, Burguera JA, Ferrell RE, Kostic V, Leroy E, Leube B, Mota-Vieira L, Papapetropoulos T, Pericak-Vance MA, Pinkus J, ... ... Polymeropoulos MH, et al. Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 5: 401-2. PMID 10048491 DOI: 10.1093/Dnares/5.6.401 |
0.339 |
|
| 1998 |
Leroy E, Boyer R, Polymeropoulos MH. Intron-exon structure of ubiquitin c-terminal hydrolase-L1. Dna Research. 5: 397-400. PMID 10048490 DOI: 10.1093/Dnares/5.6.397 |
0.338 |
|
| 1998 |
Torres R, Polymeropoulos MH. Genomic organization and localization of the human CRMP-1 gene. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 5: 393-5. PMID 10048489 DOI: 10.1093/Dnares/5.6.393 |
0.789 |
|
| 1998 |
Leroy E, Anastasopoulos D, Konitsiotis S, Lavedan C, Polymeropoulos MH. Deletions in the Parkin gene and genetic heterogeneity in a greek family with early onset Parkinson's disease Human Genetics. 103: 424-427. PMID 9856485 DOI: 10.1007/S004390050845 |
0.404 |
|
| 1998 |
Polymeropoulos MH. Autosomal dominant Parkinson's disease Journal of Neurology. 245: 1-3. PMID 9808333 DOI: 10.1007/Pl00007740 |
0.372 |
|
| 1998 |
Lavedan C, Leroy E, Torres R, Dehejia A, Dutra A, Buchholtz S, Nussbaum RL, Polymeropoulos MH. Genomic organization and expression of the human beta-synuclein gene (SNCB). Genomics. 54: 173-5. PMID 9806846 DOI: 10.1006/Geno.1998.5556 |
0.743 |
|
| 1998 |
Leroy E, Boyer R, Auburger G, Leube B, Ulm G, Mezey E, Harta G, Brownstein MJ, Jonnalagada S, Chernova T, Dehejia A, Lavedan C, Gasser T, Steinbach PJ, Wilkinson KD, ... Polymeropoulos MH, et al. The ubiquitin pathway in Parkinson's disease. Nature. 395: 451-2. PMID 9774100 DOI: 10.1038/26652 |
0.339 |
|
| 1998 |
Polymeropoulos MH. Autosomal dominant parkinson's disease and α‐synuclein Annals of Neurology. 44. PMID 9749575 DOI: 10.1002/Ana.410440710 |
0.37 |
|
| 1998 |
Patel SB, Salen G, Hidaka H, Kwiterovich PO, Stalenhoef AF, Miettinen TA, Grundy SM, Lee MH, Rubenstein JS, Polymeropoulos MH, Brownstein MJ. Mapping a gene involved in regulating dietary cholesterol absorption. The sitosterolemia locus is found at chromosome 2p21. The Journal of Clinical Investigation. 102: 1041-4. PMID 9727073 DOI: 10.1172/Jci3963 |
0.35 |
|
| 1998 |
Knutsen T, Mickley LA, Ried T, Green ED, du Manoir S, Schröck E, Macville M, Ning Y, Robey R, Polymeropoulos M, Torres R, Fojo T. Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL. Genes, Chromosomes & Cancer. 23: 44-54. PMID 9713996 DOI: 10.1002/(Sici)1098-2264(199809)23:1<44::Aid-Gcc7>3.0.Co;2-6 |
0.751 |
|
| 1998 |
Vallada H, Curtis D, Sham P, Kunugi H, Zhao J, Murray R, McGuffin P, Nanko S, Owen M, Gill M, Collier D, Antonarakis S, Housman D, Kazazian H, Nestadt G, ... ... Polymeropoulos M, et al. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 Schizophrenia Research. 32: 115-121. PMID 9713907 DOI: 10.1016/S0920-9964(98)00048-6 |
0.325 |
|
| 1998 |
Lavedan C, Dehejia A, Pike B, Dutra A, Leroy E, Ide SE, Root H, Rubenstein J, Boyer RL, Chandrasekharappa S, Makalowska I, Nussbaum RL, Polymeropoulos MH. Contig map of the Parkinson's disease region on 4q21-q23. Dna Research : An International Journal For Rapid Publication of Reports On Genes and Genomes. 5: 19-23. PMID 9628579 DOI: 10.1093/Dnares/5.1.19 |
0.768 |
|
| 1998 |
Stumpo DJ, Eddy RL, Haley LL, Sait S, Shows TB, Lai WS, Young WS, Speer MC, Dehejia A, Polymeropoulos M, Blackshear PJ. Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects. Genomics. 49: 253-64. PMID 9598313 DOI: 10.1006/Geno.1998.5247 |
0.479 |
|
| 1998 |
Swift RG, Polymeropoulos MH, Torres R, Swift M. Predisposition of Wolfram syndrome heterozygotes to psychiatric illness. Molecular Psychiatry. 3: 86-91. PMID 9491819 |
0.734 |
|
| 1998 |
Annabi B, Hiraiwa H, Mansfield BC, Lei KJ, Ubagai T, Polymeropoulos MH, Moses SW, Parvari R, Hershkovitz E, Mandel H, Fryman M, Chou JY. The gene for glycogen-storage disease type 1b maps to chromosome 11q23. American Journal of Human Genetics. 62: 400-5. PMID 9463334 DOI: 10.1086/301727 |
0.386 |
|
| 1997 |
Becker KG, Lee IJ, Nagle JW, Canning RD, Gado AM, Torres R, Polymeropoulos MH, Massa PT, Biddison WE, Drew PD. C2H2-171: a novel human cDNA representing a developmentally regulated POZ domain/zinc finger protein preferentially expressed in brain. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 15: 891-9. PMID 9568537 DOI: 10.1016/S0736-5748(97)00034-8 |
0.72 |
|
| 1997 |
Johnson MR, Wilkin DJ, Vos HL, Luna RIOD, Dehejia AM, Polymeropoulos MH, Francomano CA. Characterization of the human extracellular matrix protein 1 gene on chromosome 1q21. Matrix Biology. 16: 289-292. PMID 9501329 DOI: 10.1016/S0945-053X(97)90017-2 |
0.459 |
|
| 1997 |
Luo G, Leroy E, Kozak CA, Polymeropoulos MH, Horowits R. Mapping of the Gene (NRAP) Encoding N-RAP in the Mouse and Human Genomes Genomics. 45: 229-232. PMID 9339382 DOI: 10.1006/Geno.1997.4917 |
0.42 |
|
| 1997 |
Nussbaum RL, Polymeropoulos MH. Genetics of Parkinson's disease Human Molecular Genetics. 6: 1687-1691. PMID 9300660 DOI: 10.1093/Hmg/6.10.1687 |
0.346 |
|
| 1997 |
Polymeropoulos MH, Lavedan C, Leroy E, Ide SE, Dehejia A, Dutra A, Pike B, Root H, Rubenstein J, Boyer R, Stenroos ES, Chandrasekharappa S, Athanassiadou A, Papapetropoulos T, Johnson WG, et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science (New York, N.Y.). 276: 2045-7. PMID 9197268 DOI: 10.1126/Science.276.5321.2045 |
0.75 |
|
| 1997 |
Becker KG, Nagle JW, Canning RD, Dehejia AM, Polymeropoulos MH, Gado AM, Biddison WE, Drew PD. Molecular Cloning and Mapping of a Novel Human KRAB Domain-Containing C2H2-Type Zinc Finger to Chromosome 7q36.1 Genomics. 41: 502-504. PMID 9169157 DOI: 10.1006/Geno.1997.4678 |
0.38 |
|
| 1997 |
Higgins JJ, Pho LT, Ide SE, Nee LE, Polymeropoulos MH. Evidence for a new spinocerebellar ataxia locus. Movement Disorders : Official Journal of the Movement Disorder Society. 12: 412-7. PMID 9159738 DOI: 10.1002/Mds.870120322 |
0.739 |
|
| 1997 |
Higgins JJ, Ide SE, Oghalai JS, Polymeropoulos MH. Lack of mutations in the biotin-binding region of the pyruvate carboxylase (PC) gene in a family with partial PC deficiency. Clinical Biochemistry. 30: 79-81. PMID 9056115 DOI: 10.1016/S0009-9120(96)00125-7 |
0.734 |
|
| 1997 |
Gracia E, Ray ME, Polymeropoulos MH, Dehejia A, Meltzer PS, Trent JM. Isolation of chromosome-specific ESTs by microdissection-mediated cDNA capture Genome Research. 7: 100-107. PMID 9049628 DOI: 10.1101/Gr.7.2.100 |
0.428 |
|
| 1997 |
Freedman R, Coon H, Myles-Worsley M, Orr-Urtreger A, Olincy A, Davis A, Polymeropoulos M, Holik J, Hopkins J, Hoff M, Rosenthal J, Waldo MC, Reimherr F, Wender P, Yaw J, et al. Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proceedings of the National Academy of Sciences of the United States of America. 94: 587-92. PMID 9012828 DOI: 10.1073/Pnas.94.2.587 |
0.316 |
|
| 1996 |
Polymeropoulos MH, Ide SE, Becker K, Naylor SL. Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22. Cancer Genetics and Cytogenetics. 92: 46-9. PMID 8956871 DOI: 10.1016/S0165-4608(96)00148-3 |
0.757 |
|
| 1996 |
Polymeropoulos MH, Ide SE, Magyari T, Francomano CA. Brachydactyly type C gene maps to human chromsome 12q24. Genomics. 38: 45-50. PMID 8954778 DOI: 10.1006/Geno.1996.0590 |
0.769 |
|
| 1996 |
Johnson MR, Polymeropoulos MH, Vos HL, Luna RIOd, Francomano CA. A nonsense mutation in the cathepsin K gene observed in a family with pycnodysostosis. Genome Research. 6: 1050-1055. PMID 8938428 DOI: 10.1101/Gr.6.11.1050 |
0.406 |
|
| 1996 |
Polymeropoulos MH, Higgins JJ, Golbe LI, Johnson WG, Ide SE, Di Iorio G, Sanges G, Stenroos ES, Pho LT, Schaffer AA, Lazzarini AM, Nussbaum RL, Duvoisin RC. Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science (New York, N.Y.). 274: 1197-9. PMID 8895469 DOI: 10.1126/Science.274.5290.1197 |
0.742 |
|
| 1996 |
Ide SE, Ortiz de Luna RI, Francomano CA, Polymeropoulos MH. Exclusion of the MSX1 homeobox gene as the gene for the Ellis van Creveld syndrome in the Amish. Human Genetics. 98: 572-5. PMID 8882877 |
0.77 |
|
| 1996 |
Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, ... ... Polymeropoulos MH, et al. A gene map of the human genome. Science (New York, N.Y.). 274: 540-6. PMID 8849440 DOI: 10.1126/Science.274.5287.540 |
0.795 |
|
| 1996 |
McDowell G, Isogai T, Tanigami A, Hazelwood S, Ledbetter D, Polymeropoulos MH, Lichter-Konecki U, Konecki D, Town MM, Van't Hoff WV, Weissenbach J, Gahl WA. Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13. Biochemical and Molecular Medicine. 58: 135-41. PMID 8812732 DOI: 10.1006/Bmme.1996.0041 |
0.464 |
|
| 1996 |
Zinovieva RD, Duncan MK, Johnson TR, Torres R, Polymeropoulos MH, Tomarev SI. Structure and chromosomal localization of the human homeobox gene Prox 1. Genomics. 35: 517-22. PMID 8812486 DOI: 10.1006/Geno.1996.0392 |
0.786 |
|
| 1996 |
Polymeropoulos MH, Ide SE, Wright M, Goodship J, Weissenbach J, Pyeritz RE, Da Silva EO, Ortiz De Luna RI, Francomano CA. The gene for the Ellis-van Creveld syndrome is located on chromosome 4p16. Genomics. 35: 1-5. PMID 8661097 DOI: 10.1006/Geno.1996.0315 |
0.78 |
|
| 1996 |
Lennon G, Auffray C, Polymeropoulos M, Soares MB. The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression. Genomics. 33: 151-2. PMID 8617505 DOI: 10.1006/Geno.1996.0177 |
0.302 |
|
| 1996 |
Lee HY, Murata J, Clair T, Polymeropoulos MH, Torres R, Manrow RE, Liotta LA, Stracke ML. Cloning, chromosomal localization, and tissue expression of autotaxin from human teratocarcinoma cells. Biochemical and Biophysical Research Communications. 218: 714-9. PMID 8579579 DOI: 10.1006/Bbrc.1996.0127 |
0.739 |
|
| 1996 |
Higgins JJ, Nee LE, Vasconcelos O, Ide SE, Lavedan C, Goldfarb LG, Polymeropoulos MH. Mutations in American families with spinocerebellar ataxia (SCA) type 3: SCA3 is allelic to Machado-Joseph disease. Neurology. 46: 208-13. PMID 8559377 DOI: 10.1212/Wnl.46.1.208 |
0.738 |
|
| 1996 |
Polymeropoulos MH, Ide S, Soares MB, Lennon GG. Sequence characterization and genetic mapping of the human VSNL1 gene, a homologue of the rat visinin-like peptide RNVP1. Genomics. 29: 273-5. PMID 8530085 DOI: 10.1006/Geno.1995.1244 |
0.761 |
|
| 1995 |
Pappas GJ, Polymeropoulos MH, Boyle JM, Trent JM. Regional assignment by hybrid mapping of 36 expressed sequence tags (ESTs) on human chromosome 6. Genomics. 25: 124-9. PMID 7774909 DOI: 10.1016/0888-7543(95)80117-5 |
0.44 |
|
| 1995 |
McDowell GA, Gahl WA, Stephenson LA, Schneider JA, Weissenbach J, Polymeropoulos MH, Town MM, Hoff Wv, Farrall M, Mathew CG. Linkage of the gene for cystinosis to markers on the short arm of chromosome 17 Nature Genetics. 10: 246-248. PMID 7663525 DOI: 10.1038/Ng0695-246 |
0.415 |
|
| 1995 |
Polymeropoulos MH, Ortiz De Luna RI, Ide SE, Torres R, Rubenstein J, Francomano CA. The gene for pycnodysostosis maps to human chromosome 1cen-q21. Nature Genetics. 10: 238-9. PMID 7663522 DOI: 10.1038/Ng0695-238 |
0.789 |
|
| 1995 |
Polymeropoulos MH, Torres R, Yanovski JA, Chandrasekharappa SC, Ledbetter DH. The human corticotropin-releasing factor receptor (CRHR) gene maps to chromosome 17q12-q22. Genomics. 28: 123-4. PMID 7590738 DOI: 10.1006/Geno.1995.1118 |
0.754 |
|
| 1995 |
Polymeropoulos MH, Poush J, Rubenstein JR, Francomano CA. Localization of the gene (SYM1) for proximal symphalangism to human chromosome 17q21-q22. Genomics. 27: 225-9. PMID 7557985 DOI: 10.1006/Geno.1995.1035 |
0.431 |
|
| 1994 |
Polymeropoulos MH, Swift RG, Swift M. Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4. Nature Genetics. 8: 95-7. PMID 7987399 DOI: 10.1038/Ng0994-95 |
0.441 |
|
| 1994 |
James MR, Richard CW, Schott J-, Yousry C, Clark K, Bell J, Terwilliger JD, Kazan J, Dubay C, Vignal A, Agrapart M, Imai T, Nakamura Y, Polymeropoulos M, Weissenbach J, et al. A radiation hybrid map of 506 STS markers spanning human chromosome 11. Nature Genetics. 8: 70-76. PMID 7987395 DOI: 10.1038/Ng0994-70 |
0.392 |
|
| 1994 |
Heinzmann C, Kojis TL, Gonzalez P, Rao PV, Zigler JS, Polymeropoulos MH, Klisak I, Sparkes RS, Mohandas T, Bateman JB. Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphisms. Genomics. 23: 403-7. PMID 7835889 DOI: 10.1006/Geno.1994.1516 |
0.446 |
|
| 1994 |
Gerken S, Fish K, Uyar D, Polymeropoulos MH, Bradley P, White R, Overhauser J, Silverman GA. Integration of 28 STSs into the Physical Map of Human Chromosome 18 Genomics. 24: 612-613. PMID 7713522 DOI: 10.1006/Geno.1994.1679 |
0.477 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Ide SE, Merril CR. Dinucleotide repeat polymorphism at the D14S99E locus. Human Molecular Genetics. 2: 490. PMID 8504315 DOI: 10.1093/Hmg/2.4.490 |
0.724 |
|
| 1993 |
Carstea ED, Polymeropoulos MH, Parker CC, Detera-Wadleigh SD, O'Neill RR, Patterson MC, Goldin E, Xiao H, Straub RE, Vanier MT. Linkage of Niemann-Pick disease type C to human chromosome 18. Proceedings of the National Academy of Sciences of the United States of America. 90: 2002-4. PMID 8446622 DOI: 10.1073/Pnas.90.5.2002 |
0.318 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Sikela JM, Adams M, Venter JC, Merril CR. Chromosomal distribution of 320 genes from a brain cDNA library. Nature Genetics. 4: 381-6. PMID 8401586 DOI: 10.1038/Ng0893-381 |
0.467 |
|
| 1993 |
Xiao H, Ide SE, Merril CR, Polymeropoulos MH. Dinucleotide repeat polymorphism at the D11S982E locus. Human Molecular Genetics. 2: 1081. PMID 8364557 DOI: 10.1093/hmg/2.7.1081-a |
0.708 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the D9S147E locus. Human Molecular Genetics. 1: 549. PMID 1307259 DOI: 10.1093/Hmg/1.7.549-A |
0.327 |
|
| 1993 |
Xiao H, Merril CR, Polymeropoulos MH. Dinucleotide repeat polymorphism at the D7S476 locus. Human Molecular Genetics. 1: 549. PMID 1307258 DOI: 10.1093/Hmg/1.7.549 |
0.349 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the D5S356 locus. Human Molecular Genetics. 1: 290. PMID 1303204 DOI: 10.1093/Hmg/1.4.290 |
0.349 |
|
| 1993 |
Xiao H, Merril CR, Polymeropoulos MH. Dinucleotide repeat polymorphism at the D3S1229 locus. Human Molecular Genetics. 1: 290. PMID 1303203 DOI: 10.1093/Hmg/1.4.290-A |
0.349 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the D18S74E locus. Human Molecular Genetics. 1: 779. PMID 1302621 DOI: 10.1093/Hmg/1.9.779-A |
0.327 |
|
| 1993 |
Xiao H, Merril CR, Polymeropoulos MH. Dinucleotide repeat polymorphisms at the D3S1246 and D3S1247 loci. Human Molecular Genetics. 1: 652. PMID 1301177 DOI: 10.1093/Hmg/1.8.652 |
0.356 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human c-myc oncogene locus (MYC). Human Molecular Genetics. 1: 65. PMID 1301140 DOI: 10.1093/Hmg/1.1.65 |
0.334 |
|
| 1993 |
Polymeropoulos MH, Xiao H, Merril CR. Tetranucleotide repeat polymorphism at the human myelin basic protein gene (MBP). Human Molecular Genetics. 1: 658. PMID 1284472 DOI: 10.1093/Hmg/1.8.658 |
0.372 |
|
| 1992 |
Polymeropoulos MH, Xiao H, Merril CR. The human D5 dopamine receptor (DRD5) maps on chromosome 4. Genomics. 11: 777-8. PMID 1774076 DOI: 10.1016/0888-7543(91)90091-R |
0.332 |
|
| 1992 |
Polymeropoulos MH, Xiao H, Glodek A, Gorski M, Adams MD, Moreno RF, Fitzgerald MG, Venter JC, Merril CR. Chromosomal assignment of 46 brain cDNAs. Genomics. 12: 492-6. PMID 1559700 DOI: 10.1016/0888-7543(92)90439-Y |
0.432 |
|
| 1992 |
Khan AS, Wilcox AS, Polymeropoulos MH, Hopkins JA, Stevens TJ, Robinson M, Orpana AK, Sikela JM. Single pass sequencing and physical and genetic mapping of human brain cDNAs. Nature Genetics. 2: 180-5. PMID 1345165 DOI: 10.1038/Ng1192-180 |
0.425 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Trinucleotide repeat polymorphism at the human intestinal fatty acid binding protein gene (FABP2). Nucleic Acids Research. 18: 7198. PMID 2263509 DOI: 10.1093/Nar/18.23.7198-A |
0.346 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human thrombospondin gene (THBS1). Nucleic Acids Research. 18: 7467. PMID 2259648 DOI: 10.1093/Nar/18.24.7467 |
0.421 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human fms-related tyrosine kinase gene (FLT1). Nucleic Acids Research. 19: 2803. PMID 2041764 DOI: 10.1093/Nar/19.10.2803-A |
0.359 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human cysteine-proteinase inhibitor pseudogene (CSTP1). Nucleic Acids Research. 19: 1164. PMID 2020557 DOI: 10.1093/Nar/19.5.1164 |
0.331 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. A simple sequence repeat polymorphism at the human growth hormone locus. Nucleic Acids Research. 19: 689. PMID 2011542 DOI: 10.1093/Nar/19.3.689 |
0.328 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Tetranucleotide repeat polymorphism at the human aromatase cytochrome P-450 gene (CYP19). Nucleic Acids Research. 19: 195. PMID 2011509 DOI: 10.1093/Nar/19.1.195 |
0.4 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human gene for insulin-like growth afctor I (IGFI) Nucleic Acids Research. 19: 5797-5797. PMID 1945863 DOI: 10.1093/Nar/19.20.5797-A |
0.339 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human MHC class I CD8 alpha-chain (Leu-2/T8) gene. Nucleic Acids Research. 19: 1718. PMID 1902951 DOI: 10.1093/Nar/19.7.1718-A |
0.31 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Trinucleotide repeat polymorphism at the human gamma-B-crystallin gene. Nucleic Acids Research. 19: 4571. PMID 1886794 DOI: 10.1093/Nar/19.16.4571 |
0.379 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Trinucleotide repeat polymorphism at the human transcription factor IID gene. Nucleic Acids Research. 19: 4307. PMID 1870994 DOI: 10.1093/Nar/19.15.4307 |
0.385 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human liver-type 6-phosphofructokinase (PFKL) gene. Nucleic Acids Research. 19: 2517. PMID 1828296 DOI: 10.1093/Nar/19.9.2517 |
0.364 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human ankyrin gene (ANK1). Nucleic Acids Research. 19: 969. PMID 1826765 DOI: 10.1093/Nar/19.4.969 |
0.421 |
|
| 1991 |
Weber JL, Polymeropoulos MH, May PE, Kwitek AE, Xiao H, McPherson JD, Wasmuth JJ. Mapping of human chromosome 5 microsatellite DNA polymorphisms. Genomics. 11: 695-700. PMID 1774070 DOI: 10.1016/0888-7543(91)90077-R |
0.414 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human beta 1 subunit of the GABAA receptor gene (GABRB1). Nucleic Acids Research. 19: 6345. PMID 1659691 DOI: 10.1093/Nar/19.22.6345 |
0.344 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human debrisoquine 4-hydroxylase (CYP2D) locus Nucleic Acids Research. 19: 1961-1961. DOI: 10.1093/Nar/19.8.1961-A |
0.371 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human gene of the light and heavy chains of myeloperoxidase glycoprotein (MPO) Nucleic Acids Research. 19: 1961-1961. DOI: 10.1093/Nar/19.8.1961 |
0.36 |
|
| 1991 |
Polymeropoulos M, Xiao H, Rath D, Merril C. Dinucleotide repeat polymorphism at the human interleukin 9 gene Nucleic Acids Research. 19: 688-688. DOI: 10.1093/Nar/19.3.688-A |
0.418 |
|
| 1991 |
Polymeropoulos M, Rath D, Xiao H, Merril C. Dinucleotide repeat polymorphism at the human preproglucagon gene Nucleic Acids Research. 19: 688-688. DOI: 10.1093/Nar/19.3.688 |
0.42 |
|
| 1991 |
Polymeropoulos M, Xiao H, Rath D, Merril C. Tetranucleotide repeat polymorphism at the human dihydrofolate reductase psi-2 pseudogene (DHFRP2) Nucleic Acids Research. 19: 4792-4792. DOI: 10.1093/Nar/19.17.4792-A |
0.351 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Tetranucleotide repeat polymorphism at the human prostatic acid phosphatase (ACPP) gene Nucleic Acids Research. 19: 4792-4792. DOI: 10.1093/Nar/19.17.4792 |
0.335 |
|
| 1991 |
Polymeropoulos M, Rath D, Xiao H, Merril C. Tetranucleotide repeat polymorphism at the human coagulation factor XIII A subunit gene (F13A1) Nucleic Acids Research. 19: 4306-4306. DOI: 10.1093/Nar/19.15.4306-A |
0.398 |
|
| 1991 |
Polymeropoulos M, Xiao H, Rath D, Merril C. Trinucleotide repeat polymorphism at the human met-tRNA-i gene 1 (TRMI) Nucleic Acids Research. 19: 4306-4306. DOI: 10.1093/Nar/19.15.4306 |
0.42 |
|
| 1991 |
Polymeropoulos MH, Rath DS, Xiao H, Merril CR. Dinucleotide repeat polymorphism at the human ATP synthase beta subunit gene (ATPSB) Nucleic Acids Research. 19: 4019-4019. DOI: 10.1093/Nar/19.14.4019-A |
0.346 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human cardiac beta-myosin gene Nucleic Acids Research. 19: 4019-4019. DOI: 10.1093/Nar/19.14.4019 |
0.343 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human CTLA4 gene Nucleic Acids Research. 19: 4018-4018. DOI: 10.1093/Nar/19.14.4018-A |
0.419 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Dinucleotide repeat polymorphism at the human non-histone chromosomal protein HMG14 gene Nucleic Acids Research. 19: 3753-3753. DOI: 10.1093/Nar/19.13.3753-A |
0.428 |
|
| 1991 |
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH) Nucleic Acids Research. 19: 3753-3753. DOI: 10.1093/Nar/19.13.3753 |
0.386 |
|
| 1990 |
Weber JL, Kwitek AE, May PE, Polymeropoulos M. Dinucleotide repeat polymorphism at the D12S43 locus. Nucleic Acids Research. 18: 4637. PMID 2388861 DOI: 10.1093/Nar/18.15.4637-A |
0.349 |
|
| 1990 |
Weber JL, Kwitek AE, May PE, Polymeropoulos MH, Ledbetter S. Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci. Nucleic Acids Research. 18: 4037. PMID 1973839 DOI: 10.1093/Nar/18.13.4037 |
0.321 |
|
| 1990 |
Polymeropoulos M, Rath D, Xiao H, Merril C. Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2) Nucleic Acids Research. 18: 7468-7468. DOI: 10.1093/Nar/18.24.7468-A |
0.397 |
|
| 1990 |
Polymeropoulos M, Xiao H, Rath D, Merril C. Dinucleotide repeat polymorphism at the int-2 proto-oncogene locus (INT2) Nucleic Acids Research. 18: 7468-7468. DOI: 10.1093/Nar/18.24.7468 |
0.34 |
|
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