| Year |
Citation |
Score |
| 2008 |
Dick DM, Aliev F, Wang JC, Saccone S, Hinrichs A, Bertelsen S, Budde J, Saccone N, Foroud T, Nurnberger J, Xuei X, Conneally PM, Schuckit M, Almasy L, Crowe R, et al. A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9. Biological Psychiatry. 63: 1047-53. PMID 18163977 DOI: 10.1016/J.Biopsych.2007.11.005 |
0.311 |
|
| 2006 |
Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gómez-Tortosa E, García CA, Suchowersky O, Klimek ML, ... ... Conneally PM, et al. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. Bmc Medical Genetics. 7: 71. PMID 16914060 DOI: 10.1186/1471-2350-7-71 |
0.438 |
|
| 2006 |
Pankratz N, Byder L, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T, Nichols WC. Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 45-9. PMID 16116614 DOI: 10.1002/Mds.20663 |
0.373 |
|
| 2005 |
Koller DL, Ichikawa S, Johnson ML, Lai D, Xuei X, Edenberg HJ, Conneally PM, Hui SL, Johnston CC, Peacock M, Foroud T, Econs MJ. Contribution of the LRP5 gene to normal variation in peak BMD in women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 75-80. PMID 15619672 DOI: 10.1359/Jbmr.041019 |
0.629 |
|
| 2004 |
Nichols WC, Uniacke SK, Pankratz N, Reed T, Simon DK, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 649-55. PMID 15197702 DOI: 10.1002/Mds.20097 |
0.331 |
|
| 2004 |
Wexler NS, Lorimer J, Porter J, Gomez F, Moskowitz C, Shackell E, Marder K, Penchaszadeh G, Roberts SA, Gayán J, Brocklebank D, Cherny SS, Cardon LR, Gray J, Dlouhy SR, ... ... Conneally PM, et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proceedings of the National Academy of Sciences of the United States of America. 101: 3498-503. PMID 14993615 DOI: 10.1073/Pnas.0308679101 |
0.396 |
|
| 2004 |
Econs MJ, Koller DL, Hui SL, Fishburn T, Conneally PM, Johnston CC, Peacock M, Foroud TM. Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women. American Journal of Human Genetics. 74: 223-8. PMID 14730478 DOI: 10.1086/381401 |
0.643 |
|
| 2004 |
Bierut LJ, Rice JP, Goate A, Hinrichs AL, Saccone NL, Foroud T, Edenberg HJ, Cloninger CR, Begleiter H, Conneally PM, Crowe RR, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, et al. A genomic scan for habitual smoking in families of alcoholics: common and specific genetic factors in substance dependence. American Journal of Medical Genetics. Part A. 124: 19-27. PMID 14679582 DOI: 10.1002/Ajmg.A.20329 |
0.362 |
|
| 2003 |
Liu Y, Xu F, Recker RR, Deng HW, Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Interpretation of Genetic Linkage Findings (multiple letters) Journal of Bone and Mineral Research. 18: 2077-2080. PMID 14606522 DOI: 10.1359/Jbmr.2003.18.11.2077 |
0.558 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Human Molecular Genetics. 12: 2599-608. PMID 12925570 DOI: 10.1093/Hmg/Ddg270 |
0.416 |
|
| 2003 |
Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1057-65. PMID 12817759 DOI: 10.1359/Jbmr.2003.18.6.1057 |
0.597 |
|
| 2003 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Significant linkage of Parkinson disease to chromosome 2q36-37. American Journal of Human Genetics. 72: 1053-7. PMID 12638082 DOI: 10.1086/374383 |
0.378 |
|
| 2002 |
Close Kirkwood S, Siemers E, Viken RJ, Hodes ME, Conneally PM, Christian JC, Foroud T. Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales. Journal of Psychiatric Research. 36: 377-82. PMID 12393306 DOI: 10.1016/S0022-3956(02)00054-7 |
0.378 |
|
| 2002 |
Kirkwood SC, Siemers E, Viken R, Hodes ME, Conneally PM, Christian JC, Foroud T. Longitudinal personality changes among presymptomatic Huntington disease gene carriers. Neuropsychiatry, Neuropsychology, and Behavioral Neurology. 15: 192-7. PMID 12218712 |
0.724 |
|
| 2002 |
Carn G, Koller DL, Peacock M, Hui SL, Evans WE, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13. The Journal of Clinical Endocrinology and Metabolism. 87: 3819-24. PMID 12161516 DOI: 10.1210/Jcem.87.8.8740 |
0.67 |
|
| 2002 |
Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. American Journal of Human Genetics. 71: 124-35. PMID 12058349 DOI: 10.1086/341282 |
0.394 |
|
| 2002 |
Li YJ, Scott WK, Hedges DJ, Zhang F, Gaskell PC, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Allen FA, Goetz CG, ... ... Conneally PM, et al. Age at onset in two common neurodegenerative diseases is genetically controlled. American Journal of Human Genetics. 70: 985-93. PMID 11875758 DOI: 10.1086/339815 |
0.4 |
|
| 2001 |
Koller DL, Liu G, Econs MJ, Hui SL, Morin PA, Joslyn G, Rodriguez LA, Conneally PM, Christian JC, Johnston CC, Foroud T, Peacock M. Genome screen for quantitative trait loci underlying normal variation in femoral structure. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 16: 985-91. PMID 11393795 DOI: 10.1359/Jbmr.2001.16.6.985 |
0.638 |
|
| 2001 |
Kirkwood SC, Su JL, Conneally PM, Foroud T. Progression of symptoms in the early and middle stages of Huntington disease Archives of Neurology. 58: 273-278. PMID 11176966 DOI: 10.1001/Archneur.58.2.273 |
0.685 |
|
| 2000 |
Kirkwood SC, Siemers E, Hodes ME, Conneally PM, Christian JC, Foroud T. Subtle changes among presymptomatic carriers of the Huntington's disease gene. Journal of Neurology, Neurosurgery, and Psychiatry. 69: 773-9. PMID 11080230 DOI: 10.1136/Jnnp.69.6.773 |
0.727 |
|
| 2000 |
Koller DL, Econs MJ, Morin PA, Christian JC, Hui SL, Parry P, Curran ME, Rodriguez LA, Conneally PM, Joslyn G, Peacock M, Johnston CC, Foroud T. Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. The Journal of Clinical Endocrinology and Metabolism. 85: 3116-20. PMID 10999795 DOI: 10.1210/Jcem.85.9.6778 |
0.615 |
|
| 2000 |
Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li TK, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping. Alcoholism, Clinical and Experimental Research. 24: 933-45. PMID 10923994 |
0.621 |
|
| 2000 |
Kirkwood SC, Siemers E, Bond C, Conneally PM, Christian JC, Foroud T. Confirmation of subtle motor changes among presymptomatic carriers of the Huntington disease gene. Archives of Neurology. 57: 1040-4. PMID 10891987 DOI: 10.1001/Archneur.57.7.1040 |
0.714 |
|
| 2000 |
Martin ER, Lai EH, Gilbert JR, Rogala AR, Afshari AJ, Riley J, Finch KL, Stevens JF, Livak KJ, Slotterbeck BD, Slifer SH, Warren LL, Conneally PM, Schmechel DE, Purvis I, et al. SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer disease. American Journal of Human Genetics. 67: 383-94. PMID 10869235 DOI: 10.1086/303003 |
0.396 |
|
| 2000 |
Takacs I, Koller DL, Peacock M, Christian JC, Evans WE, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. Bone. 27: 169-73. PMID 10865225 DOI: 10.1016/S8756-3282(00)00296-9 |
0.571 |
|
| 2000 |
Scott WK, Grubber JM, Conneally PM, Small GW, Hulette CM, Rosenberg CK, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity. American Journal of Human Genetics. 66: 922-32. PMID 10712207 DOI: 10.1086/302828 |
0.343 |
|
| 2000 |
Bierut LJ, Rice JP, Edenberg HJ, Goate A, Foroud T, Cloninger CR, Begleiter H, Conneally PM, Crowe RR, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, Schuckit MA, Reich T. Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking. American Journal of Medical Genetics. 90: 299-302. PMID 10710227 DOI: 10.1002/(Sici)1096-8628(20000214)90:4<299::Aid-Ajmg7>3.0.Co;2-Y |
0.318 |
|
| 2000 |
Martin ER, Gilbert JR, Lai EH, Riley J, Rogala AR, Slotterbeck BD, Sipe CA, Grubber JM, Warren LL, Conneally PM, Saunders AM, Schmechel DE, Purvis I, Pericak-Vance MA, Roses AD, et al. Analysis of association at single nucleotide polymorphisms in the APOE region. Genomics. 63: 7-12. PMID 10662539 DOI: 10.1006/Geno.1999.6057 |
0.358 |
|
| 2000 |
Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li T, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism Susceptibility Loci: Confirmation Studies in a Replicate Sample and Further Mapping Alcoholism: Clinical and Experimental Research. 24: 933-945. DOI: 10.1111/J.1530-0277.2000.Tb04634.X |
0.651 |
|
| 2000 |
Scott WK, Grubber JM, Conneally P, Small GW, Gilbert JR, Haines JL, Pericak-Vance MA. Fine-mapping of the chromosome 12 Alzheimer disease locus using family-based association tests of microsatellite markers Neurobiology of Aging. 21: 129. DOI: 10.1016/S0197-4580(00)82380-5 |
0.403 |
|
| 1999 |
Takacs I, Koller DL, Peacock M, Christian JC, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. The Journal of Clinical Endocrinology and Metabolism. 84: 4467-71. PMID 10599704 DOI: 10.1210/Jcem.84.12.6179 |
0.629 |
|
| 1999 |
Kirkwood SC, Siemers E, Stout JC, Hodes ME, Conneally PM, Christian JC, Foroud T. Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Archives of Neurology. 56: 563-8. PMID 10328251 DOI: 10.1001/Archneur.56.5.563 |
0.736 |
|
| 1999 |
Rogaeva EA, Premkumar S, Grubber J, Serneels L, Scott WK, Kawarai T, Song Y, Hill DL, Abou-Donia SM, Martin ER, Vance JJ, Yu G, Orlacchio A, Pei Y, Nishimura M, ... ... Conneally PM, et al. An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease. Nature Genetics. 22: 19-22. PMID 10319855 DOI: 10.1038/8729 |
0.348 |
|
| 1998 |
Scott WK, Yamaoka LH, Bass MP, Gaskell PC, Conneally PM, Small GW, Farrer LA, Auerbach SA, Saunders AM, Roses AD, Haines JL, Pericak-Vance MA. No genetic association between the LRP receptor and sporadic or late-onset familial Alzheimer disease. Neurogenetics. 1: 179-83. PMID 10737120 DOI: 10.1007/S100480050026 |
0.4 |
|
| 1998 |
Foroud T, Bucholz KK, Edenberg HJ, Goate A, Neuman RJ, Porjesz B, Koller DL, Rice J, Reich T, Bierut LJ, Cloninger CR, Nurnberger JI, Li TK, Conneally PM, Tischfield JA, et al. Linkage of an alcoholism-related severity phenotype to chromosome 16. Alcoholism, Clinical and Experimental Research. 22: 2035-42. PMID 9884148 DOI: 10.1097/00000374-199812000-00020 |
0.591 |
|
| 1998 |
Koller DL, Rodriguez LA, Christian JC, Slemenda CW, Econs MJ, Hui SL, Morin P, Conneally PM, Joslyn G, Curran ME, Peacock M, Johnston CC, Foroud T. Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 13: 1903-8. PMID 9844108 DOI: 10.1359/Jbmr.1998.13.12.1903 |
0.635 |
|
| 1998 |
Edenberg HJ, Reynolds J, Koller DL, Begleiter H, Bucholz KK, Conneally PM, Crowe R, Goate A, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, Reich T, Rice JP, Schuckit M, et al. A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence. Alcoholism, Clinical and Experimental Research. 22: 1080-5. PMID 9726278 |
0.576 |
|
| 1998 |
Reich T, Edenberg HJ, Goate A, Williams JT, Rice JP, Van Eerdewegh P, Foroud T, Hesselbrock V, Schuckit MA, Bucholz K, Porjesz B, Li TK, Conneally PM, Nurnberger JI, Tischfield JA, et al. Genome-wide search for genes affecting the risk for alcohol dependence. American Journal of Medical Genetics. 81: 207-15. PMID 9603606 DOI: 10.1002/(Sici)1096-8628(19980508)81:3<207::Aid-Ajmg1>3.0.Co;2-T |
0.378 |
|
| 1998 |
Edenberg HJ, Foroud T, Koller DL, Goate A, Rice J, Van Eerdewegh P, Reich T, Cloninger CR, Nurnberger JI, Kowalczuk M, Wu B, Li TK, Conneally PM, Tischfield JA, Wu W, et al. A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism. Alcoholism, Clinical and Experimental Research. 22: 505-12. PMID 9581660 |
0.561 |
|
| 1998 |
Pericak-Vance MA, Bass ML, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Saunders AM, Roses AD, Haines JL. Complete genomic screen in late-onset familial Alzheimer's disease. Neurobiology of Aging. 19: S39-42. PMID 9562466 DOI: 10.1016/S0197-4580(98)00037-2 |
0.317 |
|
| 1998 |
Edenberg HJ, Reynolds J, Koller DL, Begleiter H, Bucholz KK, Conneally PM, Crowe R, Goate A, Hesselbrock V, Li T, Numberger JI, Porjesz B, Reich T, Rice JP, Schuckit M, et al. A Family-Based Analysis of Whether the Functional Promoter Alleles of the Serotonin Transporter Gene HTT Affect the Risk for Alcohol Dependence Alcoholism: Clinical and Experimental Research. 22: 1080-1085. DOI: 10.1111/J.1530-0277.1998.Tb03704.X |
0.371 |
|
| 1998 |
Foroud T, Bucholz KK, Edenberg HJ, Goate A, Neuman RJ, Porjesz B, Koller DL, Ric J, Reich T, Bierut LJ, Cloninger CR, Nurnberger JI, Li T, Conneally PM, Tischfield JA, et al. Linkage of an Alcoholism-Related Severity Phenotype to Chromosome 16 Alcoholism: Clinical and Experimental Research. 22: 2035-2042. DOI: 10.1097/00000374-199812000-00020 |
0.395 |
|
| 1997 |
Pericak-Vance MA, Bass MP, Yamaoka LH, Gaskell PC, Scott WK, Terwedow HA, Menold MM, Conneally PM, Small GW, Vance JM, Saunders AM, Roses AD, Haines JL. Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12. Jama. 278: 1237-41. PMID 9333264 DOI: 10.1001/Jama.1997.03550150041033 |
0.453 |
|
| 1997 |
Loyd JE, Slovis B, Phillips JA, Butler MG, Foroud TM, Conneally PM, Newman JH. The presence of genetic anticipation suggests that the molecular basis of familial primary pulmonary hypertension may be trinucleotide repeat expansion. Chest. 111: 82S-83S. PMID 9184540 DOI: 10.1378/Chest.111.6_Supplement.82S |
0.306 |
|
| 1997 |
Edenberg HJ, Foroud T, Conneally PM, Sorbel JJ, Carr K, Crose C, Willig C, Zhao J, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Rice JP, Goate A, et al. Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 3, 5, 15, 16, 17, and 22. American Journal of Medical Genetics. 74: 238-46. PMID 9184305 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<238::Aid-Ajmg2>3.0.Co;2-M |
0.419 |
|
| 1997 |
Nurnberger JI, DePaulo JR, Gershon ES, Reich T, Blehar MC, Edenberg HJ, Foroud T, Miller M, Bowman E, Mayeda A, Rau NL, Smiley C, Conneally PM, McMahon F, Meyers D, et al. Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report American Journal of Medical Genetics - Neuropsychiatric Genetics. 74: 227-237. PMID 9184304 DOI: 10.1002/(Sici)1096-8628(19970531)74:3<227::Aid-Ajmg1>3.0.Co;2-N |
0.372 |
|
| 1997 |
Small GW, Noble EP, Matsuyama SS, Jarvik LF, Komo S, Kaplan A, Ritchie T, Pritchard ML, Saunders AM, Conneally PM, Roses AD, Haines JL, Pericak-Vance MA. D2 dopamine receptor A1 allele in Alzheimer disease and aging. Archives of Neurology. 54: 281-5. PMID 9074397 DOI: 10.1001/Archneur.1997.00550150041014 |
0.32 |
|
| 1997 |
Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nature Genetics. 15: 277-80. PMID 9054941 DOI: 10.1038/Ng0397-277 |
0.63 |
|
| 1996 |
Haines JL, Pritchard ML, Saunders AM, Schildkraut JM, Growdon JH, Gaskell PC, Farrer LA, Auerbach SA, Gusella JF, Locke PA, Rosi BL, Yamaoka L, Small GW, Conneally PM, Roses AD, et al. No association between alpha 1-antichymotrypsin and familial Alzheimer's disease. Annals of the New York Academy of Sciences. 802: 35-41. PMID 8993482 DOI: 10.1111/J.1749-6632.1996.Tb32596.X |
0.34 |
|
| 1996 |
Quaid KA, Dinwiddie H, Conneally PM, Nurnberger JI. Issues in genetic testing for susceptibility to alcoholism: lessons from Alzheimer's disease and Huntington's disease. Alcoholism, Clinical and Experimental Research. 20: 1430-7. PMID 8947321 DOI: 10.1111/J.1530-0277.1996.Tb01145.X |
0.391 |
|
| 1996 |
Siemers E, Foroud T, Bill DJ, Sorbel J, Norton JA, Hodes ME, Niebler G, Conneally PM, Christian JC. Motor changes in presymptomatic Huntington disease gene carriers. Archives of Neurology. 53: 487-92. PMID 8660148 DOI: 10.1001/Archneur.1996.00550060029011 |
0.383 |
|
| 1995 |
Allamand V, Broux O, Bourg N, Richard I, Tischfield JA, Hodes ME, Conneally PM, Fardeau M, Jackson CE, Beckmann JS. Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locus. Human Molecular Genetics. 4: 459-63. PMID 7795603 DOI: 10.1093/Hmg/4.3.459 |
0.328 |
|
| 1995 |
Foroud T, Siemers E, Kleindorfer D, Bill DJ, Hodes ME, Norton JA, Conneally PM, Christian JC. Cognitive scores in carriers of Huntington's disease gene compared to noncarriers. Annals of Neurology. 37: 657-64. PMID 7755361 DOI: 10.1002/Ana.410370516 |
0.431 |
|
| 1993 |
Velinov M, Sarfarazi M, Young K, Hodes ME, Conneally PM, Jackson CE, Tsipouras P. Limb-girdle muscular dystrophy is closely linked to the fibrillin locus on chromosome 15. Connective Tissue Research. 29: 13-21. PMID 8339542 DOI: 10.3109/03008209309061962 |
0.337 |
|
| 1993 |
Locke PA, MacDonald ME, Srinidhi J, Gilliam TC, Tanzi RE, Conneally PM, Wexler NS, Haines JL, Gusella JF. A genetic linkage map of the chromosome 4 short arm. Somatic Cell and Molecular Genetics. 19: 95-101. PMID 8096345 DOI: 10.1007/Bf01233958 |
0.395 |
|
| 1993 |
Lebo RV, Chance PF, Dyck PJ, Redila-Flores MT, Lynch ED, Golbus MS, Bird TD, King MC, Anderson LA, Hall J, Wiegant J, Jiang Z, Dazin PF, Punnett HH, Schonberg SA, ... ... Conneally PM, et al. Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fcγ receptor gene region Human Genetics. 91: 301. DOI: 10.1007/BF00218282 |
0.304 |
|
| 1992 |
Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. Nature Genetics. 1: 68-71. PMID 1363810 DOI: 10.1038/Ng0492-68 |
0.308 |
|
| 1992 |
Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene. Nature Genetics. 1: 64-7. PMID 1363809 DOI: 10.1038/Ng0492-64 |
0.404 |
|
| 1991 |
Conneally PM. Locating disease genes through linkage. Special problems in working with tuberous sclerosis. Annals of the New York Academy of Sciences. 615: 252-5. PMID 2039149 DOI: 10.1111/J.1749-6632.1991.Tb37766.X |
0.352 |
|
| 1991 |
Haines JL, Amos J, Attwood J, Bech-Hansen NT, Burley M, Conneally PM, Connor JM, Fahsold R, Flodman P, Fryer A. Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative dataset. Annals of the New York Academy of Sciences. 615: 256-64. PMID 1674844 DOI: 10.1111/J.1749-6632.1991.Tb37767.X |
0.301 |
|
| 1989 |
St George-Hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally PM, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: progress and problems. Neurobiology of Aging. 10: 417-25. PMID 2682321 DOI: 10.1016/0197-4580(89)90082-1 |
0.361 |
|
| 1989 |
Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB. Huntington disease: no evidence for locus heterogeneity. Genomics. 5: 304-8. PMID 2571579 DOI: 10.1016/0888-7543(89)90062-1 |
0.373 |
|
| 1989 |
Rouleau GA, Haines JL, Bazanowski A, Colella-Crowley A, Trofatter JA, Wexler NS, Conneally PM, Gusella JF. A genetic linkage map of the long arm of human chromosome 22. Genomics. 4: 1-6. PMID 2563348 DOI: 10.1016/0888-7543(89)90306-6 |
0.429 |
|
| 1988 |
Tanzi RE, Haines JL, Watkins PC, Stewart GD, Wallace MR, Hallewell R, Wong C, Wexler NS, Conneally PM, Gusella JF. Genetic linkage map of human chromosome 21. Genomics. 3: 129-36. PMID 2906323 DOI: 10.1016/0888-7543(88)90143-7 |
0.457 |
|
| 1988 |
Ozelius L, Hsu YPP, Bruns G, Powell JF, Chen S, Weyler W, Utterback M, Zucker D, Haines J, Trofatter JA, Conneally PM, Gusella JF, Breakefield XO. Human monoamine oxidase gene (MAOA): Chromosome position (Xp21-p11) and DNA polymorphism Genomics. 3: 53-58. PMID 2906043 DOI: 10.1016/0888-7543(88)90159-0 |
0.384 |
|
| 1988 |
Haines JL, Ozelius L, St George-Hyslop P, Wexler NS, Gusella JF, Conneally PM. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes. Genetic Epidemiology. 5: 375-80. PMID 2905314 DOI: 10.1002/Gepi.1370050602 |
0.397 |
|
| 1988 |
Kambouris M, Dlouhy SR, Trofatter JA, Conneally PM, Hodes ME. Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28. American Journal of Medical Genetics. 29: 239-46. PMID 2894172 DOI: 10.1002/Ajmg.1320290138 |
0.377 |
|
| 1987 |
St George-Hyslop P, Polinsky R, Haines J, Nee L, Tanzi R, Conneally P, Growdon J, Myers R, Pollen D, Drachman D. Search for the familial Alzheimer's disease gene. Journal of Neural Transmission. Supplementum. 24: 13-21. PMID 2890708 |
0.355 |
|
| 1987 |
Rouleau GA, Wertelecki W, Haines JL, Hobbs WJ, Trofatter JA, Seizinger BR, Martuza RL, Superneau DW, Conneally PM, Gusella JF. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. Nature. 329: 246-8. PMID 2888021 DOI: 10.1038/329246A0 |
0.44 |
|
| 1987 |
Tanzi RE, St George-Hyslop PH, Haines JL, Polinsky RJ, Nee L, Foncin JF, Neve RL, McClatchey AI, Conneally PM, Gusella JF. The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene. Nature. 329: 156-7. PMID 2888020 DOI: 10.1038/329156A0 |
0.418 |
|
| 1987 |
Gilliam TC, Tanzi RE, Haines JL, Bonner TI, Faryniarz AG, Hobbs WJ, MacDonald ME, Cheng SV, Folstein SE, Conneally PM. Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere. Cell. 50: 565-71. PMID 2886227 DOI: 10.1016/0092-8674(87)90029-8 |
0.472 |
|
| 1986 |
Baehner RL, Kunkel LM, Monaco AP, Haines JL, Conneally PM, Palmer C, Heerema N, Orkin SH. DNA linkage analysis of X chromosome-linked chronic granulomatous disease Proceedings of the National Academy of Sciences of the United States of America. 83: 3398-3401. PMID 3010296 DOI: 10.1073/Pnas.83.10.3398 |
0.322 |
|
| 1986 |
Gusella JF, Gilliam TC, Tanzi RE, MacDonald ME, Cheng SV, Wallace M, Haines J, Conneally PM, Wexler NS. Molecular genetics of Huntington's disease. Cold Spring Harbor Symposia On Quantitative Biology. 51: 359-64. PMID 2884064 DOI: 10.1101/Sqb.1986.051.01.043 |
0.32 |
|
| 1986 |
Wallace MR, Conneally PM, Long GL, Benson MD. Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family. American Journal of Medical Genetics. 25: 335-41. PMID 2877582 DOI: 10.1002/Ajmg.1320250220 |
0.376 |
|
| 1985 |
Conneally PM. Genetic diseases: Probe for muscular dystrophy Nature. 316: 763-764. PMID 4033778 DOI: 10.1038/316763A0 |
0.352 |
|
| 1985 |
Frydman M, Bonne-Tamir B, Farrer LA, Conneally PM, Magazanik A, Ashbel S, Goldwitch Z. Assignment of the gene for Wilson disease to chromosome 13: Linkage to the esterase D locus Proceedings of the National Academy of Sciences of the United States of America. 82: 1819-1921. PMID 3856863 DOI: 10.1073/pnas.82.6.1819 |
0.364 |
|
| 1985 |
Wexler NS, Conneally PM, Housman D, Gusella JF. A DNA Polymorphism for Huntington's Disease Marks the Future Archives of Neurology. 42: 20-24. PMID 3155610 DOI: 10.1001/Archneur.1985.04060010026009 |
0.382 |
|
| 1984 |
Conneally PM, Wallace MR, Gusella JF, Wexler NS. Huntington disease: Estimation of heterozygote status using linked genetic markers Genetic Epidemiology. 1: 81-88. PMID 6242401 DOI: 10.1002/Gepi.1370010110 |
0.416 |
|
| 1983 |
Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE, Watkins PC, Ottina K, Wallace MR, Sakaguchi AY, Young AB, Shoulson I, Bonilla E, Martin JB. A polymorphic DNA marker genetically linked to Huntington's disease Nature. 306: 234-238. PMID 6316146 DOI: 10.1038/306234A0 |
0.441 |
|
| 1981 |
Al-Nassar KE, Palmer CG, Conneally PM, Yu PL. The genetic structure of the kuwaiti population II: The distribution of Q-band chromosomal heteromorphisms Human Genetics. 57: 423-427. PMID 7286984 DOI: 10.1007/Bf00281697 |
0.341 |
|
| 1981 |
Al-Nassar KE, Conneally PM, Palmer CG, Yu Pl. The genetic structure of the Kuwaiti population - I. Distribution of 17 markers with genetic distance analysis Human Genetics. 57: 192-198. PMID 7228033 DOI: 10.1007/Bf00282021 |
0.342 |
|
| 1980 |
Conneally PM, Rivas ML. Linkage analysis in man Advances in Human Genetics. 10: 209-266. PMID 6994459 DOI: 10.1007/978-1-4615-8288-5_3 |
0.41 |
|
| 1978 |
Escobar V, Conneally PM, Lopez C. The dentition of the Queckchi Indians. Anthropological aspects. American Journal of Physical Anthropology. 47: 443-51. PMID 931025 DOI: 10.1002/Ajpa.1330470316 |
0.315 |
|
| 1976 |
Escobar V, Melnick M, Conneally PM. The inheritance of bilateral rotation of maxillary central incisors American Journal of Physical Anthropology. 45: 109-115. DOI: 10.1002/Ajpa.1330450114 |
0.369 |
|
| 1971 |
Bixler D, Fogh-Andersen P, Conneally PM. Incidence of cleft lip and palate in the offspring of cleft parents. Clinical Genetics. 2: 155-9. PMID 5111759 DOI: 10.1111/J.1399-0004.1971.Tb00271.X |
0.321 |
|
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