| Year |
Citation |
Score |
| 2022 |
Orlova E, Dudding T, Chernus JM, Alotaibi RN, Haworth S, Crout RJ, Lee MK, Mukhopadhyay N, Feingold E, Levy SM, McNeil DW, Foxman B, Weyant RJ, Timpson NJ, Marazita ML, et al. Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study. Genes. 14. PMID 36672800 DOI: 10.3390/genes14010059 |
0.312 |
|
| 2022 |
Mukhopadhyay N, Feingold E, Moreno-Uribe L, Wehby G, Valencia-Ramirez LC, Restrepo Muñeton CP, Padilla C, Deleyiannis F, Christensen K, Poletta FA, Orioli IM, Hecht JT, Buxó CJ, Butali A, Adeyemo WL, et al. Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes. Genetic Epidemiology. PMID 35191549 DOI: 10.1002/gepi.22447 |
0.331 |
|
| 2021 |
Liu C, Lee MK, Naqvi S, Hoskens H, Liu D, White JD, Indencleef K, Matthews H, Eller RJ, Li J, Mohammed J, Swigut T, Richmond S, Manyama M, Hallgrímsson B, ... Feingold E, et al. Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Plos Genetics. 17: e1009695. PMID 34411106 DOI: 10.1371/journal.pgen.1009695 |
0.312 |
|
| 2020 |
Aslam MM, Jalil F, John P, Fan KH, Bhatti A, Feingold E, Demirci FY, Kamboh MI. A sequencing study of CTLA4 in Pakistani rheumatoid arthritis cases. Plos One. 15: e0239426. PMID 32946523 DOI: 10.1371/Journal.Pone.0239426 |
0.342 |
|
| 2020 |
Aslam MM, John P, Fan KH, Bhatti A, Aziz W, Ahmed B, Feingold E, Demirci FY, Kamboh MI. Investigating the GWAS-Implicated Loci for Rheumatoid Arthritis in the Pakistani Population. Disease Markers. 2020: 1910215. PMID 32831971 DOI: 10.1155/2020/1910215 |
0.345 |
|
| 2020 |
Cheema AN, Pirim D, Wang X, Ali J, Bhatti A, John P, Feingold E, Demirci FY, Kamboh MI. Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population. Disease Markers. 2020: 9738567. PMID 32685059 DOI: 10.1155/2020/9738567 |
0.369 |
|
| 2020 |
Fan KH, Feingold E, Rosenthal SL, Demirci FY, Ganguli M, Lopez OL, Kamboh MI. Whole-Exome Sequencing Analysis of Alzheimer's Disease in Non-APOE*4 Carriers. Journal of Alzheimer's Disease : Jad. PMID 32651314 DOI: 10.3233/Jad-200037 |
0.412 |
|
| 2020 |
Bishop MR, Diaz Perez KK, Sun M, Ho S, Chopra P, Mukhopadhyay N, Hetmanski JB, Taub MA, Moreno-Uribe LM, Valencia-Ramirez LC, Restrepo Muñeton CP, Wehby G, Hecht JT, Deleyiannis F, Weinberg SM, ... ... Feingold E, et al. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios. American Journal of Human Genetics. PMID 32574564 DOI: 10.1016/J.Ajhg.2020.05.018 |
0.354 |
|
| 2019 |
Mukhopadhyay N, Bishop M, Mortillo M, Chopra P, Hetmanski JB, Taub MA, Moreno LM, Valencia-Ramirez LC, Restrepo C, Wehby GL, Hecht JT, Deleyiannis F, Butali A, Weinberg SM, Beaty TH, ... ... Feingold E, et al. Whole genome sequencing of orofacial cleft trios from the Gabriella Miller Kids First Pediatric Research Consortium identifies a new locus on chromosome 21. Human Genetics. PMID 31848685 DOI: 10.1007/S00439-019-02099-1 |
0.433 |
|
| 2019 |
Chernus JM, Allen EG, Zeng Z, Hoffman ER, Hassold TJ, Feingold E, Sherman SL. A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Plos Genetics. 15: e1008414. PMID 31830031 DOI: 10.1371/Journal.Pgen.1008414 |
0.413 |
|
| 2019 |
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, de Jong MA, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, et al. Novel genetic loci affecting facial shape variation in humans. Elife. 8. PMID 31763980 DOI: 10.7554/Elife.49898 |
0.388 |
|
| 2019 |
Orlova E, Carlson JC, Lee MK, Feingold E, McNeil DW, Crout RJ, Weyant RJ, Marazita ML, Shaffer JR. Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Bmc Oral Health. 19: 215. PMID 31533690 DOI: 10.1186/S12903-019-0904-4 |
0.371 |
|
| 2019 |
Aslam MM, John P, Fan KH, Bhatti A, Jahangir S, Feingold E, Demirci FY, Kamboh MI. Exploration of shared genetic susceptibility loci between type 1 diabetes and rheumatoid arthritis in the Pakistani population. Bmc Research Notes. 12: 544. PMID 31455420 DOI: 10.1186/S13104-019-4590-8 |
0.344 |
|
| 2019 |
Brown AL, de Smith AJ, Gant VU, Yang W, Scheurer ME, Walsh KM, Chernus JM, Kallsen NA, Peyton SA, Davies GE, Ehli EA, Winick N, Heerema NA, Carroll AJ, Borowitz MJ, ... ... Feingold E, et al. Inherited genetic susceptibility of acute lymphoblastic leukemia in Down syndrome. Blood. PMID 31350265 DOI: 10.1182/Blood.2018890764 |
0.401 |
|
| 2019 |
Carlson JC, Anand D, Butali A, Buxo CJ, Christensen K, Deleyiannis F, Hecht JT, Moreno LM, Orioli IM, Padilla C, Shaffer JR, Vieira AR, Wehby GL, Weinberg SM, Murray JC, ... ... Feingold E, et al. A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals. Genetic Epidemiology. PMID 31172578 DOI: 10.1002/Gepi.22214 |
0.398 |
|
| 2019 |
Kamboh MI, Fan KH, Yan Q, Beer JC, Snitz BE, Wang X, Chang CH, Demirci FY, Feingold E, Ganguli M. Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Neurobiology of Aging. PMID 30954325 DOI: 10.1016/J.Neurobiolaging.2019.02.024 |
0.357 |
|
| 2019 |
Pirim D, Radwan ZH, Wang X, Niemsiri V, Hokanson JE, Hamman RF, Feingold E, Bunker CH, Demirci FY, Kamboh MI. Apolipoprotein E-C1-C4-C2 gene cluster region and inter-individual variation in plasma lipoprotein levels: a comprehensive genetic association study in two ethnic groups. Plos One. 14: e0214060. PMID 30913229 DOI: 10.1371/Journal.Pone.0214060 |
0.404 |
|
| 2019 |
Xiong Z, Dankova G, Howe LJ, Lee MK, Hysi PG, Jong MAd, Zhu G, Adhikari K, Li D, Li Y, Pan B, Feingold E, Marazita ML, Shaffer JR, McAloney K, et al. Author response: Novel genetic loci affecting facial shape variation in humans Elife. DOI: 10.7554/Elife.49898.Sa2 |
0.32 |
|
| 2018 |
Shaffer JR, LeClair J, Carlson JC, Feingold E, Buxó CJ, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Murray JC, et al. Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts. American Journal of Medical Genetics. Part A. PMID 30582786 DOI: 10.1002/Ajmg.A.61002 |
0.385 |
|
| 2018 |
Indencleef K, Roosenboom J, Hoskens H, White JD, Shriver MD, Richmond S, Peeters H, Feingold E, Marazita ML, Shaffer JR, Weinberg SM, Hens G, Claes P. Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation. Frontiers in Genetics. 9: 502. PMID 30410503 DOI: 10.3389/Fgene.2018.00502 |
0.416 |
|
| 2018 |
Roosenboom J, Indencleef K, Lee MK, Hoskens H, White JD, Liu D, Hecht JT, Wehby GL, Moreno LM, Hodges-Simeon C, Feingold E, Marazita ML, Richmond S, Shriver MD, Claes P, et al. SNPs Associated With Testosterone Levels Influence Human Facial Morphology. Frontiers in Genetics. 9: 497. PMID 30405702 DOI: 10.3389/Fgene.2018.00497 |
0.394 |
|
| 2018 |
Yan Q, Nho K, Del-Aguila JL, Wang X, Risacher SL, Fan KH, Snitz BE, Aizenstein HJ, Mathis CA, Lopez OL, Demirci FY, Feingold E, Klunk WE, Saykin AJ, et al. Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging. Molecular Psychiatry. PMID 30361487 DOI: 10.1038/S41380-018-0246-7 |
0.347 |
|
| 2018 |
Carlson JC, Nidey NL, Butali A, Buxo CJ, Christensen K, Deleyiannis FW, Hecht JT, Field LL, Moreno-Uribe LM, Orioli IM, Poletta FA, Padilla C, Vieira AR, Weinberg SM, Wehby GL, ... Feingold E, et al. Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts. Genetic Epidemiology. PMID 30277614 DOI: 10.1002/Gepi.22158 |
0.398 |
|
| 2018 |
Howe LJ, Lee MK, Sharp GC, Davey Smith G, St Pourcain B, Shaffer JR, Ludwig KU, Mangold E, Marazita ML, Feingold E, Zhurov A, Stergiakouli E, Sandy J, Richmond S, Weinberg SM, et al. Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. Plos Genetics. 14: e1007501. PMID 30067744 DOI: 10.1371/Journal.Pgen.1007501 |
0.421 |
|
| 2018 |
Özbek U, Lin HM, Lin Y, Weeks DE, Chen W, Shaffer JR, Purcell SM, Feingold E. Statistics for X-chromosome associations. Genetic Epidemiology. PMID 29900581 DOI: 10.1002/Gepi.22132 |
0.358 |
|
| 2018 |
Govil M, Mukhopadhyay N, Weeks DE, Feingold E, Shaffer JR, Levy SM, Vieira AR, Slayton RL, McNeil DW, Weyant RJ, Crout RJ, Marazita ML. Novel caries loci in children and adults implicated by genome-wide analysis of families. Bmc Oral Health. 18: 98. PMID 29859070 DOI: 10.1186/S12903-018-0559-6 |
0.336 |
|
| 2018 |
Chernus J, Roosenboom J, Ford M, Lee MK, Emanuele B, Anderton J, Hecht JT, Padilla C, Deleyiannis FWB, Buxo CJ, Feingold E, Leslie EJ, Shaffer JR, Weinberg SM, Marazita ML. GWAS reveals loci associated with velopharyngeal dysfunction. Scientific Reports. 8: 8470. PMID 29855589 DOI: 10.1038/S41598-018-26880-W |
0.422 |
|
| 2018 |
Roosenboom J, Lee MK, Hecht JT, Heike CL, Wehby GL, Christensen K, Feingold E, Marazita ML, Maga AM, Shaffer JR, Weinberg SM. Mapping genetic variants for cranial vault shape in humans. Plos One. 13: e0196148. PMID 29698431 DOI: 10.1371/Journal.Pone.0196148 |
0.436 |
|
| 2018 |
Claes P, Roosenboom J, White JD, Swigut T, Sero D, Li J, Lee MK, Zaidi A, Mattern BC, Liebowitz C, Pearson L, González T, Leslie EJ, Carlson JC, Orlova E, ... ... Feingold E, et al. Genome-wide mapping of global-to-local genetic effects on human facial shape. Nature Genetics. PMID 29459680 DOI: 10.1038/S41588-018-0057-4 |
0.375 |
|
| 2017 |
Dilek P, Radwan ZH, Wang X, Waqar F, Niemsiri V, Hokanson JE, Hamman RF, Bunker CH, Barmada MM, Feingold E, Demirci FY, Kamboh MI. A comprehensive association study of apolipoprotein E-C1-C4-C2 gene cluster variation with plasma lipoprotein traits. Atherosclerosis. 263: e83. PMID 29366240 DOI: 10.1016/J.Atherosclerosis.2017.06.270 |
0.339 |
|
| 2017 |
Shaffer JR, Li J, Lee MK, Roosenboom J, Orlova E, Adhikari K, Gallo C, Poletti G, Schuler-Faccini L, Bortolini MC, Canizales-Quinteros S, Rothhammer F, Bedoya G, González-José R, ... ... Feingold E, et al. Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment. American Journal of Human Genetics. 101: 913-924. PMID 29198719 DOI: 10.1016/J.Ajhg.2017.10.001 |
0.441 |
|
| 2017 |
Carlson JC, Standley J, Petrin A, Shaffer JR, Butali A, Buxó CJ, Castilla E, Christensen K, Deleyiannis FW, Hecht JT, Field LL, Garidkhuu A, Moreno Uribe LM, Nagato N, Orioli IM, ... ... Feingold E, et al. Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes. Genetic Epidemiology. PMID 29124805 DOI: 10.1002/Gepi.22090 |
0.432 |
|
| 2017 |
Bhaumik P, Ghosh P, Ghosh S, Feingold E, Ozbek U, Sarkar B, Dey SK. Combined association of Presenilin-1 and Apolipoprotein E polymorphisms with maternal meiosis II error in Down syndrome births. Genetics and Molecular Biology. 0. PMID 28767121 DOI: 10.1590/1678-4685-Gmb-2016-0138 |
0.381 |
|
| 2017 |
Carlson JC, Taub MA, Feingold E, Beaty TH, Murray JC, Marazita ML, Leslie EJ. Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. Birth Defects Research. 109: 1030-1038. PMID 28762674 DOI: 10.1002/Bdr2.23605 |
0.355 |
|
| 2017 |
Lee MK, Shaffer JR, Leslie EJ, Orlova E, Carlson JC, Feingold E, Marazita ML, Weinberg SM. Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Plos One. 12: e0176566. PMID 28441456 DOI: 10.1371/Journal.Pone.0176566 |
0.447 |
|
| 2017 |
Leslie EJ, Carlson JC, Shaffer JR, Buxó CJ, Castilla EE, Christensen K, Deleyiannis FWB, Field LL, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, Feingold E, et al. Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate. American Journal of Medical Genetics. Part A. PMID 28425186 DOI: 10.1002/Ajmg.A.38210 |
0.398 |
|
| 2017 |
Lewis DD, Shaffer JR, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML. Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries. International Journal of Dentistry. 2017: 8465125. PMID 28348596 DOI: 10.1155/2017/8465125 |
0.326 |
|
| 2017 |
Demirci FY, Wang X, Morris DL, Feingold E, Bernatsky S, Pineau C, Clarke A, Ramsey-Goldman R, Manzi S, Vyse TJ, Ilyas Kamboh M. Multiple signals at the extended 8p23 locus are associated with susceptibility to systemic lupus erythematosus. Journal of Medical Genetics. PMID 28289186 DOI: 10.1136/Jmedgenet-2016-104247 |
0.339 |
|
| 2017 |
Eckert S, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR. Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental caries. Journal of Human Genetics. PMID 28100911 DOI: 10.1038/Jhg.2016.161 |
0.434 |
|
| 2017 |
Leslie EJ, Carlson JC, Shaffer JR, Butali A, Buxó CJ, Castilla EE, Christensen K, Deleyiannis FW, Leigh Field L, Hecht JT, Moreno L, Orioli IM, Padilla C, Vieira AR, Wehby GL, ... Feingold E, et al. Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Human Genetics. PMID 28054174 DOI: 10.1007/S00439-016-1754-7 |
0.446 |
|
| 2016 |
Begum F, Chowdhury R, Cheung V, Sherman S, Feingold E. Genome-Wide Association Study of Meiotic Recombination Phenotypes. G3 (Bethesda, Md.). PMID 27733454 DOI: 10.1534/G3.116.035766 |
0.435 |
|
| 2016 |
Shaffer JR, Orlova E, Lee MK, Leslie EJ, Raffensperger ZD, Heike CL, Cunningham ML, Hecht JT, Kau CH, Nidey NL, Moreno LM, Wehby GL, Murray JC, Laurie CA, Laurie CC, ... ... Feingold E, et al. Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Plos Genetics. 12: e1006149. PMID 27560520 DOI: 10.1371/Journal.Pgen.1006149 |
0.443 |
|
| 2016 |
Uzun A, Sahin Y, Schuster JS, Zheng X, Ryckman K, Feingold E, Padbury J. Structural and Genomic Variation in Preterm Birth. Pediatric Research. PMID 27466897 DOI: 10.1038/Pr.2016.152 |
0.346 |
|
| 2016 |
Leslie EJ, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, Vieira AR, et al. A multi-ethnic genome-wide association study identifies novel loci for nonsyndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q31. Human Molecular Genetics. PMID 27033726 DOI: 10.1093/Hmg/Ddw104 |
0.418 |
|
| 2016 |
Leslie EJ, Liu H, Carlson JC, Shaffer JR, Feingold E, Wehby G, Laurie CA, Jain D, Laurie CC, Doheny KF, McHenry T, Resick J, Sanchez C, Jacobs J, Emanuele B, et al. A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. American Journal of Human Genetics. PMID 27018472 DOI: 10.1016/J.Ajhg.2016.02.014 |
0.418 |
|
| 2016 |
Begum F, Sharker MH, Sherman SL, Tseng GC, Feingold E. Regionally Smoothed Meta-Analysis Methods for GWAS Datasets. Genetic Epidemiology. 40: 154-60. PMID 26707090 DOI: 10.1002/Gepi.21949 |
0.411 |
|
| 2015 |
Zeng Z, Weeks DE, Chen W, Mukhopadhyay N, Feingold E. A Pipeline for Classifying Relationships Using Dense SNP/SNV Data and Putative Pedigree Information. Genetic Epidemiology. PMID 26709242 DOI: 10.1002/Gepi.21948 |
0.374 |
|
| 2015 |
Özbek U, Feingold E, Weeks DE. Efficient Identification of Null-Allele Single Nucleotide Polymorphism Markers. Human Heredity. 80: 79-89. PMID 26613255 DOI: 10.1159/000441279 |
0.397 |
|
| 2015 |
Demirci FY, Wang X, Kelly JA, Morris DL, Barmada MM, Feingold E, Kao AH, Sivils KL, Bernatsky S, Pineau C, Clarke A, Ramsey-Goldman R, Vyse TJ, Gaffney PM, Manzi S, et al. Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26316170 DOI: 10.1002/Art.39403 |
0.38 |
|
| 2015 |
Ramachandran D, Zeng Z, Locke AE, Mulle JG, Bean LJ, Rosser TC, Dooley KJ, Cua CL, Capone GT, Reeves RH, Maslen CL, Cutler DJ, Feingold E, Sherman SL, Zwick ME. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. G3 (Bethesda, Md.). 5: 1961-71. PMID 26194203 DOI: 10.1534/G3.115.019943 |
0.404 |
|
| 2015 |
Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. Genome-wide copy-number variation study of psychosis in Alzheimer's disease. Translational Psychiatry. 5: e574. PMID 26035058 DOI: 10.1038/Tp.2015.64 |
0.33 |
|
| 2015 |
Wolf ZT, Brand HA, Shaffer JR, Leslie EJ, Arzi B, Willet CE, Cox TC, McHenry T, Narayan N, Feingold E, Wang X, Sliskovic S, Karmi N, Safra N, Sanchez C, et al. Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palate. Plos Genetics. 11: e1005059. PMID 25798845 DOI: 10.1371/Journal.Pgen.1005059 |
0.405 |
|
| 2015 |
Wang X, Lopez O, Sweet RA, Becker JT, DeKosky ST, Barmada MM, Feingold E, Demirci FY, Kamboh MI. Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. Journal of Alzheimer's Disease : Jad. 45: 651-8. PMID 25649651 DOI: 10.3233/Jad-142442 |
0.395 |
|
| 2015 |
Shaffer JR, Carlson JC, Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, et al. Effects of enamel matrix genes on dental caries are moderated by fluoride exposures. Human Genetics. 134: 159-67. PMID 25373699 DOI: 10.1007/S00439-014-1504-7 |
0.409 |
|
| 2014 |
Zheng X, Demirci FY, Barmada MM, Richardson GA, Lopez OL, Sweet RA, Kamboh MI, Feingold E. A rare duplication on chromosome 16p11.2 is identified in patients with psychosis in Alzheimer's disease. Plos One. 9: e111462. PMID 25379732 DOI: 10.1371/Journal.Pone.0111462 |
0.321 |
|
| 2014 |
Oliver TR, Middlebrooks CD, Tinker SW, Allen EG, Bean LJ, Begum F, Feingold E, Chowdhury R, Cheung V, Sherman SL. An examination of the relationship between hotspots and recombination associated with chromosome 21 nondisjunction. Plos One. 9: e99560. PMID 24926858 DOI: 10.1371/Journal.Pone.0099560 |
0.373 |
|
| 2014 |
Stanley BO, Feingold E, Cooper M, Vanyukov MM, Maher BS, Slayton RL, Willing MC, Reis SE, McNeil DW, Crout RJ, Weyant RJ, Levy SM, Vieira AR, Marazita ML, Shaffer JR. Genetic Association of MPPED2 and ACTN2 with Dental Caries. Journal of Dental Research. 93: 626-632. PMID 24810274 DOI: 10.1177/0022034514534688 |
0.425 |
|
| 2014 |
Zeng Z, Feingold E, Wang X, Weeks DE, Lee M, Cuenco DT, Broffitt B, Weyant RJ, Crout R, McNeil DW, Levy SM, Marazita ML, Shaffer JR. Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries. Caries Research. 48: 330-8. PMID 24556642 DOI: 10.1159/000356299 |
0.397 |
|
| 2014 |
Shaffer JR, Polk DE, Wang X, Feingold E, Weeks DE, Lee MK, Cuenco KT, Weyant RJ, Crout RJ, McNeil DW, Marazita ML. Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. G3 (Bethesda, Md.). 4: 307-14. PMID 24347629 DOI: 10.1534/G3.113.008755 |
0.448 |
|
| 2014 |
Middlebrooks CD, Mukhopadhyay N, Tinker SW, Allen EG, Bean LJ, Begum F, Chowdhury R, Cheung V, Doheny K, Adams M, Feingold E, Sherman SL. Evidence for dysregulation of genome-wide recombination in oocytes with nondisjoined chromosomes 21. Human Molecular Genetics. 23: 408-17. PMID 24014426 DOI: 10.1093/Hmg/Ddt433 |
0.309 |
|
| 2013 |
Zheng X, Feingold E, Ryckman KK, Shaffer JR, Boyd HA, Feenstra B, Melbye M, Marazita ML, Murray JC, Cuenco KT. Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. Frontiers in Genetics. 4: 196. PMID 24194744 DOI: 10.3389/Fgene.2013.00196 |
0.368 |
|
| 2013 |
Wang Q, Jia P, Cuenco KT, Feingold E, Marazita ML, Wang L, Zhao Z. Multi-dimensional prioritization of dental caries candidate genes and its enriched dense network modules. Plos One. 8: e76666. PMID 24146904 DOI: 10.1371/Journal.Pone.0076666 |
0.32 |
|
| 2013 |
Wang Q, Jia P, Cuenco KT, Zeng Z, Feingold E, Marazita ML, Wang L, Zhao Z. Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies. Plos One. 8: e72653. PMID 23967329 DOI: 10.1371/Journal.Pone.0072653 |
0.386 |
|
| 2013 |
Zeng Z, Shaffer JR, Wang X, Feingold E, Weeks DE, Lee M, Cuenco KT, Wendell SK, Weyant RJ, Crout R, McNeil DW, Marazita ML. Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition. Journal of Dental Research. 92: 432-7. PMID 23470693 DOI: 10.1177/0022034513481976 |
0.348 |
|
| 2013 |
Shaffer JR, Feingold E, Wang X, Lee M, Tcuenco K, Weeks DE, Weyant RJ, Crout R, McNeil DW, Marazita ML. GWAS of dental caries patterns in the permanent dentition. Journal of Dental Research. 92: 38-44. PMID 23064961 DOI: 10.1177/0022034512463579 |
0.421 |
|
| 2012 |
Wang X, Shaffer JR, Zeng Z, Begum F, Vieira AR, Noel J, Anjomshoaa I, Cuenco KT, Lee MK, Beck J, Boerwinkle E, Cornelis MC, Hu FB, Crosslin DR, Laurie CC, ... ... Feingold E, et al. Genome-wide association scan of dental caries in the permanent dentition. Bmc Oral Health. 12: 57. PMID 23259602 DOI: 10.1186/1472-6831-12-57 |
0.421 |
|
| 2012 |
Polk DE, Wang X, Feingold E, Shaffer JR, Weeks DE, Weyant RJ, Crout RJ, McNeil DW, Marazita ML. Effects of smoking and genotype on the PSR index of periodontal disease in adults aged 18-49. International Journal of Environmental Research and Public Health. 9: 2839-50. PMID 23066400 DOI: 10.3390/Ijerph9082839 |
0.347 |
|
| 2012 |
Ackerman C, Locke AE, Feingold E, Reshey B, Espana K, Thusberg J, Mooney S, Bean LJ, Dooley KJ, Cua CL, Reeves RH, Sherman SL, Maslen CL. An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects. American Journal of Human Genetics. 91: 646-59. PMID 23040494 DOI: 10.1016/J.Ajhg.2012.08.017 |
0.371 |
|
| 2012 |
Ghosh P, Bhaumik P, Ghosh S, Ozbek U, Feingold E, Maslen C, Sarkar B, Pramanik V, Biswas P, Bandyopadhyay B, Dey SK. Polymorphic haplotypes of CRELD1 differentially predispose Down syndrome and euploids individuals to atrioventricular septal defect. American Journal of Medical Genetics. Part A. 158: 2843-8. PMID 22987595 DOI: 10.1002/Ajmg.A.35626 |
0.329 |
|
| 2012 |
Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, ... ... Feingold E, et al. Genome-wide association study of Alzheimer's disease. Translational Psychiatry. 2: e117. PMID 22832961 DOI: 10.1038/Tp.2012.45 |
0.428 |
|
| 2012 |
Zheng X, Shaffer JR, McHugh CP, Laurie CC, Feenstra B, Melbye M, Murray JC, Marazita ML, Feingold E. Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies. Genetic Epidemiology. 36: 253-62. PMID 22714937 DOI: 10.1002/Gepi.21618 |
0.349 |
|
| 2012 |
Shaffer JR, Feingold E, Marazita ML. Genome-wide association studies: prospects and challenges for oral health. Journal of Dental Research. 91: 637-41. PMID 22562461 DOI: 10.1177/0022034512446968 |
0.357 |
|
| 2012 |
Laurie CC, Laurie CA, Rice K, Doheny KF, Zelnick LR, McHugh CP, Ling H, Hetrick KN, Pugh EW, Amos C, Wei Q, Wang LE, Lee JE, Barnes KC, Hansel NN, ... ... Feingold E, et al. Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nature Genetics. 44: 642-50. PMID 22561516 DOI: 10.1038/Ng.2271 |
0.33 |
|
| 2012 |
Shaffer JR, Feingold E, Wang X, Tcuenco KT, Weeks DE, DeSensi RS, Polk DE, Wendell S, Weyant RJ, Crout R, McNeil DW, Marazita ML. Heritable patterns of tooth decay in the permanent dentition: principal components and factor analyses. Bmc Oral Health. 12: 7. PMID 22405185 DOI: 10.1186/1472-6831-12-7 |
0.319 |
|
| 2012 |
Begum F, Ghosh D, Tseng GC, Feingold E. Comprehensive literature review and statistical considerations for GWAS meta-analysis. Nucleic Acids Research. 40: 3777-84. PMID 22241776 DOI: 10.1093/Nar/Gkr1255 |
0.325 |
|
| 2012 |
Oliver TR, Tinker SW, Allen EG, Hollis N, Locke AE, Bean LJ, Chowdhury R, Begum F, Marazita M, Cheung V, Feingold E, Sherman SL. Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21. Human Genetics. 131: 1039-46. PMID 22160426 DOI: 10.1007/S00439-011-1121-7 |
0.348 |
|
| 2012 |
Kamboh MI, Barmada MM, Demirci FY, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Sweet RA, Feingold E, DeKosky ST, Lopez OL. Genome-wide association analysis of age-at-onset in Alzheimer's disease. Molecular Psychiatry. 17: 1340-6. PMID 22005931 DOI: 10.1038/Mp.2011.135 |
0.43 |
|
| 2012 |
Ryckman KK, Feenstra B, Shaffer JR, Bream EN, Geller F, Feingold E, Weeks DE, Gadow E, Cosentino V, Saleme C, Simhan HN, Merrill D, Fong CT, Busch T, Berends SK, et al. Replication of a genome-wide association study of birth weight in preterm neonates. The Journal of Pediatrics. 160: 19-24.e4. PMID 21885063 DOI: 10.1016/J.Jpeds.2011.07.038 |
0.338 |
|
| 2011 |
Ghosh S, Hong CS, Feingold E, Ghosh P, Ghosh P, Bhaumik P, Dey SK. Epidemiology of Down syndrome: new insight into the multidimensional interactions among genetic and environmental risk factors in the oocyte. American Journal of Epidemiology. 174: 1009-16. PMID 21957181 DOI: 10.1093/Aje/Kwr240 |
0.329 |
|
| 2011 |
Shaffer JR, Wang X, Feingold E, Lee M, Begum F, Weeks DE, Cuenco KT, Barmada MM, Wendell SK, Crosslin DR, Laurie CC, Doheny KF, Pugh EW, Zhang Q, Feenstra B, et al. Genome-wide association scan for childhood caries implicates novel genes. Journal of Dental Research. 90: 1457-62. PMID 21940522 DOI: 10.1177/0022034511422910 |
0.428 |
|
| 2011 |
Yang J, Manolio TA, Pasquale LR, Boerwinkle E, Caporaso N, Cunningham JM, de Andrade M, Feenstra B, Feingold E, Hayes MG, Hill WG, Landi MT, Alonso A, Lettre G, Lin P, et al. Genome partitioning of genetic variation for complex traits using common SNPs. Nature Genetics. 43: 519-25. PMID 21552263 DOI: 10.1038/Ng.823 |
0.417 |
|
| 2011 |
Zheng X, Morrison AC, Feingold E, Turner ST, Ferrell RE. Association between NEDD4L gene and sodium lithium countertransport. American Journal of Hypertension. 24: 145-8. PMID 21088674 DOI: 10.1038/Ajh.2010.222 |
0.377 |
|
| 2010 |
Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, Freeman SB, Torfs CP, Cua CL, Epstein MP, Wu MC, Lin X, Capone G, Sherman SL, Bean LJ. Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genetic Epidemiology. 34: 613-23. PMID 20718043 DOI: 10.1002/Gepi.20518 |
0.407 |
|
| 2010 |
Diergaarde B, Brand R, Lamb J, Cheong SY, Stello K, Barmada MM, Feingold E, Whitcomb DC. Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis. Pancreatology : Official Journal of the International Association of Pancreatology (Iap) ... [Et Al.]. 10: 194-200. PMID 20484958 DOI: 10.1159/000236023 |
0.355 |
|
| 2010 |
Cheung VG, Sherman SL, Feingold E. Genetics. Genetic control of hotspots. Science (New York, N.Y.). 327: 791-2. PMID 20150474 DOI: 10.1126/Science.1187155 |
0.318 |
|
| 2010 |
Cornelis MC, Agrawal A, Cole JW, Hansel NN, Barnes KC, Beaty TH, Bennett SN, Bierut LJ, Boerwinkle E, Doheny KF, Feenstra B, Feingold E, Fornage M, Haiman CA, Harris EL, et al. The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions. Genetic Epidemiology. 34: 364-72. PMID 20091798 DOI: 10.1002/Gepi.20492 |
0.419 |
|
| 2010 |
D'Angelo GM, Kamboh MI, Feingold E. A Likelihood-Based Approach for Missing Genotype Data. Human Heredity. 69: 171-83. PMID 20068333 DOI: 10.1159/000273732 |
0.394 |
|
| 2010 |
Ghosh S, Feingold E, Chakraborty S, Dey SK. Telomere length is associated with types of chromosome 21 nondisjunction: a new insight into the maternal age effect on Down syndrome birth. Human Genetics. 127: 403-9. PMID 20063167 DOI: 10.1007/S00439-009-0785-8 |
0.335 |
|
| 2010 |
Kuo CL, Feingold E. What's the best statistic for a simple test of genetic association in a case-control study? Genetic Epidemiology. 34: 246-53. PMID 20025064 DOI: 10.1002/Gepi.20455 |
0.371 |
|
| 2010 |
Mukhopadhyay I, Feingold E, Weeks DE, Thalamuthu A. Association tests using kernel-based measures of multi-locus genotype similarity between individuals. Genetic Epidemiology. 34: 213-21. PMID 19697357 DOI: 10.1002/Gepi.20451 |
0.41 |
|
| 2010 |
Boyd H, Feenstra B, Geller F, Feingold E, Ryckman K, Shaffer J, Laurie C, Zhang Q, Doheny K, Pugh E, Manolio T, Marazita M, Melbye M, Murray J, Consortium G. 292 A Genome-Wide Association Study of Spontaneous Preterm Delivery Pediatric Research. 68: 150-150. DOI: 10.1203/00006450-201011001-00292 |
0.426 |
|
| 2009 |
Chowdhury R, Bois PR, Feingold E, Sherman SL, Cheung VG. Genetic analysis of variation in human meiotic recombination. Plos Genetics. 5: e1000648. PMID 19763160 DOI: 10.1371/Journal.Pgen.1000648 |
0.416 |
|
| 2009 |
Oliver TR, Bhise A, Feingold E, Tinker S, Masse N, Sherman SL. Investigation of factors associated with paternal nondisjunction of chromosome 21. American Journal of Medical Genetics. Part A. 149: 1685-90. PMID 19606484 DOI: 10.1002/Ajmg.A.32942 |
0.309 |
|
| 2009 |
Ghosh S, Feingold E, Dey SK. Etiology of Down syndrome: Evidence for consistent association among altered meiotic recombination, nondisjunction, and maternal age across populations. American Journal of Medical Genetics. Part A. 149: 1415-20. PMID 19533770 DOI: 10.1002/Ajmg.A.32932 |
0.362 |
|
| 2009 |
Wang X, Kammerer CM, Anderson S, Lu J, Feingold E. A comparison of principal component analysis and factor analysis strategies for uncovering pleiotropic factors. Genetic Epidemiology. 33: 325-31. PMID 19048641 DOI: 10.1002/Gepi.20384 |
0.358 |
|
| 2008 |
Lin Y, Tseng GC, Cheong SY, Bean LJ, Sherman SL, Feingold E. Smarter clustering methods for SNP genotype calling. Bioinformatics (Oxford, England). 24: 2665-71. PMID 18826959 DOI: 10.1093/Bioinformatics/Btn509 |
0.31 |
|
| 2008 |
Oliver TR, Feingold E, Yu K, Cheung V, Tinker S, Yadav-Shah M, Masse N, Sherman SL. New insights into human nondisjunction of chromosome 21 in oocytes. Plos Genetics. 4: e1000033. PMID 18369452 DOI: 10.1371/Journal.Pgen.1000033 |
0.344 |
|
| 2008 |
Bhattacharjee S, Kuo CL, Mukhopadhyay N, Brock GN, Weeks DE, Feingold E. Robust score statistics for QTL linkage analysis. American Journal of Human Genetics. 82: 567-82. PMID 18304491 DOI: 10.1016/J.Ajhg.2007.11.012 |
0.321 |
|
| 2007 |
Reshmi SC, Roychoudhury S, Yu Z, Feingold E, Potter D, Saunders WS, Gollin SM. Inverted duplication pattern in anaphase bridges confirms the breakage-fusion-bridge (BFB) cycle model for 11q13 amplification. Cytogenetic and Genome Research. 116: 46-52. PMID 17268177 DOI: 10.1159/000097425 |
0.302 |
|
| 2007 |
Sundar PD, Feingold E, Minster RL, DeKosky ST, Kamboh MI. Gender-specific association of ATP-binding cassette transporter 1 (ABCA1) polymorphisms with the risk of late-onset Alzheimer's disease. Neurobiology of Aging. 28: 856-62. PMID 16725228 DOI: 10.1016/J.Neurobiolaging.2006.04.005 |
0.39 |
|
| 2006 |
O'Neill SM, Peters JA, Vogel VG, Feingold E, Rubinstein WS. Referral to cancer genetic counseling: are there stages of readiness? American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 142: 221-31. PMID 17068804 DOI: 10.1002/Ajmg.C.30109 |
0.317 |
|
| 2006 |
Mukhopadhyay I, Feingold E, Wang T, Elston RC, Weeks DE. Treatment of uninformative families in mean allele sharing tests for linkage. Statistical Applications in Genetics and Molecular Biology. 5: Article13. PMID 17049024 DOI: 10.2202/1544-6115.1206 |
0.303 |
|
| 2006 |
Jung J, Weeks DE, Feingold E. Gene-dropping vs. empirical variance estimation for allele-sharing linkage statistics. Genetic Epidemiology. 30: 652-65. PMID 16917920 DOI: 10.1002/Gepi.20177 |
0.344 |
|
| 2006 |
Sherman SL, Lamb NE, Feingold E. Relationship of recombination patterns and maternal age among non-disjoined chromosomes 21. Biochemical Society Transactions. 34: 578-80. PMID 16856865 DOI: 10.1042/Bst0340578 |
0.316 |
|
| 2006 |
Kamboh MI, Minster RL, Feingold E, DeKosky ST. Genetic association of ubiquilin with Alzheimer's disease and related quantitative measures. Molecular Psychiatry. 11: 273-9. PMID 16302009 DOI: 10.1038/Sj.Mp.4001775 |
0.431 |
|
| 2006 |
Kofler J, Fan K, Yan Q, Sweet RA, Feingold E, Lopez OL, Ilyas Kamboh M. P4-239: ASSOCIATION OF ALZHEIMER'S DISEASE GENETIC RISK VARIANTS WITH PATHOLOGY ENDOPHENOTYPES Alzheimer's & Dementia. 14: P1534-P1534. DOI: 10.1016/J.Jalz.2018.07.060 |
0.356 |
|
| 2005 |
Moffett SP, Feingold E, Barmada MM, Damcott CM, Marshall JA, Hamman RF, Ferrell RE. The C161-->T polymorphism in peroxisome proliferator-activated receptor gamma, but not P12A, is associated with insulin resistance in Hispanic and non-Hispanic white women: evidence for another functional variant in peroxisome proliferator-activated receptor gamma. Metabolism: Clinical and Experimental. 54: 1552-6. PMID 16253648 DOI: 10.1016/J.Metabol.2005.05.025 |
0.323 |
|
| 2005 |
Lamb NE, Yu K, Shaffer J, Feingold E, Sherman SL. Association between maternal age and meiotic recombination for trisomy 21 American Journal of Human Genetics. 76: 91-99. PMID 15551222 DOI: 10.1086/427266 |
0.325 |
|
| 2004 |
Broman KW, Feingold E. SNPs made routine. Nature Methods. 1: 104-5. PMID 15782170 DOI: 10.1038/Nmeth1104-104 |
0.364 |
|
| 2004 |
Kerstann KF, Feingold E, Freeman SB, Bean LJ, Pyatt R, Tinker S, Jewel AH, Capone G, Sherman SL. Linkage disequilibrium mapping in trisomic populations: analytical approaches and an application to congenital heart defects in Down syndrome. Genetic Epidemiology. 27: 240-51. PMID 15389927 DOI: 10.1002/Gepi.20019 |
0.347 |
|
| 2004 |
Mukhopadhyay I, Feingold E, Weeks DE, Visscher PM, Wray NR, Sieberts SK, Broman KW, Gudbjartsson DF, Abecasis G, Cox N, Daly MJ, Kruglyak L, Laird N, Markianos K, Patterson N, et al. No "bias" toward the null hypothesis in most conventional multipoint nonparametric linkage analyses [1] (multiple letters) American Journal of Human Genetics. 75: 716-727. PMID 15338457 DOI: 10.1086/424754 |
0.328 |
|
| 2004 |
Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in uncoupling protein 3 is associated with dietary intake and body composition in females. Metabolism: Clinical and Experimental. 53: 458-64. PMID 15045692 DOI: 10.1016/J.Metabol.2003.11.019 |
0.34 |
|
| 2004 |
Xu Z, Kerstann KF, Sherman SL, Chakravarti A, Feingold E. A trisomic transmission disequilibrium test. Genetic Epidemiology. 26: 125-31. PMID 14748012 DOI: 10.1002/Gepi.10302 |
0.364 |
|
| 2004 |
Song KK, Weeks DE, Sobel E, Feingold E. Efficient Simulation of P Values for Linkage Analysis Genetic Epidemiology. 26: 88-96. PMID 14748008 DOI: 10.1002/Gepi.10296 |
0.311 |
|
| 2003 |
Lin Y, Reynolds P, Feingold E. An empirical bayesian method for differential expression studies using one-channel microarray data. Statistical Applications in Genetics and Molecular Biology. 2: Article8. PMID 16646786 DOI: 10.2202/1544-6115.1024 |
0.305 |
|
| 2003 |
T Cuenco K, Szatkiewicz JP, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for selected sibling pairs. American Journal of Human Genetics. 73: 863-73. PMID 12970847 DOI: 10.1086/378589 |
0.319 |
|
| 2003 |
Damcott CM, Feingold E, Moffett SP, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels. Human Genetics. 112: 610-6. PMID 12634920 DOI: 10.1007/S00439-003-0937-1 |
0.362 |
|
| 2003 |
Zhang Y, Syed R, Uygar C, Pallos D, Gorry MC, Firatli E, Cortelli JR, VanDyke TE, Hart PS, Feingold E, Hart TC. Evaluation of human leukocyte N-formylpeptide receptor (FPR1) SNPs in aggressive periodontitis patients Genes and Immunity. 4: 22-29. PMID 12595898 DOI: 10.1038/Sj.Gene.6363900 |
0.327 |
|
| 2002 |
Feingold E. Regression-based quantitative-trait-locus mapping in the 21st century American Journal of Human Genetics. 71: 217-222. PMID 12154779 DOI: 10.1086/341964 |
0.32 |
|
| 2002 |
Yu K, Feingold E. Methods for analyzing the spatial distribution of chiasmata during meiosis based on recombination data Biometrics. 58: 369-377. PMID 12071410 DOI: 10.1111/J.0006-341X.2002.00369.X |
0.308 |
|
| 2002 |
Song KK, Feingold E, Weeks DE. Statistics for nonparametric linkage analysis of X-linked traits in general pedigrees American Journal of Human Genetics. 70: 181-191. PMID 11719901 DOI: 10.1086/338308 |
0.345 |
|
| 2001 |
Feingold E. Methods for linkage analysis of quantitative trait loci in humans Theoretical Population Biology. 60: 167-180. PMID 11855951 DOI: 10.1006/Tpbi.2001.1545 |
0.379 |
|
| 2001 |
Yu K, Feingold E. Estimating the frequency distribution of crossovers during meiosis from recombination data Biometrics. 57: 427-434. PMID 11414566 DOI: 10.1111/J.0006-341X.2001.00427.X |
0.315 |
|
| 2001 |
Sengul H, Weeks DE, Feingold E. A survey of affected-sibship statistics for nonparametric linkage analysis American Journal of Human Genetics. 69: 179-190. PMID 11404816 DOI: 10.1086/321264 |
0.328 |
|
| 2000 |
Kahsar-Miller M, Azziz R, Feingold E, Witchel SF. A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome Fertility and Sterility. 74: 1237-1240. PMID 11119758 DOI: 10.1016/S0015-0282(00)01620-4 |
0.309 |
|
| 2000 |
Feingold E, Song KK, Weeks DE. Comparison of allele-sharing statistics for general pedigrees Genetic Epidemiology. 19. PMID 11055376 DOI: 10.1002/1098-2272(2000)19:1+<::Aid-Gepi14>3.0.Co;2-4 |
0.331 |
|
| 2000 |
Estop AM, Cieply K, Munne S, Surti U, Wakim A, Feingold E. Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies Human Genetics. 106: 517-524. PMID 10914681 DOI: 10.1007/S004390000275 |
0.301 |
|
| 2000 |
Forrest WF, Feingold E. Composite statistics for QTL mapping with moderately discordant sibling pairs American Journal of Human Genetics. 66: 1642-1660. PMID 10762549 DOI: 10.1086/302897 |
0.325 |
|
| 2000 |
Brown AS, Feingold E, Broman KW, Sherman SL. Genome-wide variation in recombination in female meiosis: a risk factor for non-disjunction of chromosome 21. Human Molecular Genetics. 9: 515-23. PMID 10699174 DOI: 10.1093/Hmg/9.4.515 |
0.346 |
|
| 1999 |
Barmada MM, Aston CE, Feingold E. A simple allele sharing statistic for multiple locus systems Genetic Epidemiology. 17. PMID 10597482 DOI: 10.1002/Gepi.1370170780 |
0.308 |
|
| 1999 |
Estop AM, Cieply KM, Munne S, Feingold E. Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) Human Genetics. 104: 412-417. PMID 10394934 DOI: 10.1007/S004390050977 |
0.308 |
|
| 1997 |
Durham LK, Feingold E. Genome scanning for segments shared identical by descent among distant relatives in isolated populations American Journal of Human Genetics. 61: 830-842. PMID 9382093 DOI: 10.1086/514891 |
0.322 |
|
| 1997 |
Lamb NE, Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, et al. Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21 Human Molecular Genetics. 6: 1391-1399. PMID 9285774 DOI: 10.1093/Hmg/6.9.1391 |
0.346 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2013 |
Shaffer JR, Polk DE, Feingold E, Wang X, Cuenco KT, Weeks DE, DeSensi RS, Weyant RJ, Crout R, McNeil DW, Marazita ML. Demographic, socioeconomic, and behavioral factors affecting patterns of tooth decay in the permanent dentition: principal components and factor analyses. Community Dentistry and Oral Epidemiology. 41: 364-73. PMID 23106439 DOI: 10.1111/Cdoe.12016 |
0.298 |
|
| 2004 |
Damcott CM, Moffett SP, Feingold E, Barmada MM, Marshall JA, Hamman RF, Ferrell RE. Genetic variation in fatty acid-binding protein-4 and peroxisome proliferator-activated receptor gamma interactively influence insulin sensitivity and body composition in males. Metabolism: Clinical and Experimental. 53: 303-9. PMID 15015141 DOI: 10.1016/J.Metabol.2003.10.010 |
0.298 |
|
| 2011 |
Nielsen SM, Rubinstein WS, Thull DL, Armstrong MJ, Feingold E, Yip L, Tisherman SA, Carty SE. Long-term outcomes, branch-specific expressivity, and disease-related mortality in von Hippel-Lindau type 2A. Familial Cancer. 10: 701-7. PMID 21713522 DOI: 10.1007/S10689-011-9465-7 |
0.295 |
|
| 1998 |
Estop AM, Cieply KM, Wakim A, Feingold E. Meiotic products of two reciprocal translocations studied by multicolor fluorescence in situ hybridization Cytogenetics and Cell Genetics. 83: 193-198. PMID 10072576 DOI: 10.1159/000015177 |
0.294 |
|
| 2003 |
Levinson KL, Feingold E, Ferrell RE, Glover TW, Traboulsi EI, Finegold DN. Age of onset in hereditary lymphedema. The Journal of Pediatrics. 142: 704-8. PMID 12838201 DOI: 10.1067/Mpd.2003.235 |
0.293 |
|
| 2007 |
Hall HE, Surti U, Hoffner L, Shirley S, Feingold E, Hassold T. The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction. American Journal of Medical Genetics. Part A. 143: 2249-55. PMID 17705154 DOI: 10.1002/Ajmg.A.31918 |
0.293 |
|
| 2021 |
Curtis SW, Chang D, Lee MK, Shaffer JR, Indencleef K, Epstein MP, Cutler DJ, Murray JC, Feingold E, Beaty TH, Claes P, Weinberg SM, Marazita ML, Carlson JC, Leslie EJ. The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Hgg Advances. 2. PMID 33817668 DOI: 10.1016/j.xhgg.2021.100025 |
0.292 |
|
| 2008 |
Irie J, Reck B, Wu Y, Wicker LS, Howlett S, Rainbow D, Feingold E, Ridgway WM. Genome-wide microarray expression analysis of CD4+ T Cells from nonobese diabetic congenic mice identifies Cd55 (Daf1) and Acadl as candidate genes for type 1 diabetes. Journal of Immunology (Baltimore, Md. : 1950). 180: 1071-9. PMID 18178847 DOI: 10.4049/Jimmunol.180.2.1071 |
0.289 |
|
| 2012 |
Alleman BW, Myking S, Ryckman KK, Myhre R, Feingold E, Feenstra B, Geller F, Boyd HA, Shaffer JR, Zhang Q, Begum F, Crosslin D, Doheny K, Pugh E, Pay ASD, et al. No observed association for mitochondrial SNPs with preterm delivery and related outcomes Pediatric Research. 72: 539-544. PMID 22902432 DOI: 10.1038/Pr.2012.112 |
0.288 |
|
| 2004 |
Szatkiewicz JP, Feingold E. A powerful and robust new linkage statistic for discordant sibling pairs. American Journal of Human Genetics. 75: 906-9. PMID 15368196 DOI: 10.1086/425523 |
0.287 |
|
| 2023 |
Li Z, Chang TC, Junco JJ, Devidas M, Li Y, Yang W, Huang X, Hedges DJ, Cheng Z, Shago M, Carroll AJ, Heerema NA, Gastier-Foster JM, Wood BL, Borowitz MJ, ... ... Feingold E, et al. Genomic landscape of Down syndrome-associated acute lymphoblastic leukemia. Blood. PMID 37001051 DOI: 10.1182/blood.2023019765 |
0.283 |
|
| 2021 |
Chernus JM, Sherman SL, Feingold E. Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21. Prenatal Diagnosis. PMID 33596328 DOI: 10.1002/pd.5919 |
0.283 |
|
| 2001 |
Peters DG, Kassam AB, Feingold E, Heidrich-O'Hare E, Yonas H, Ferrell RE, Brufsky A. Molecular anatomy of an intracranial aneurysm: coordinated expression of genes involved in wound healing and tissue remodeling. Stroke; a Journal of Cerebral Circulation. 32: 1036-42. PMID 11283408 DOI: 10.1161/01.Str.32.4.1036 |
0.283 |
|
| 2021 |
Mukhopadhyay N, Feingold E, Moreno-Uribe L, Wehby G, Valencia-Ramirez LC, Muñeton CPR, Padilla C, Deleyiannis F, Christensen K, Poletta FA, Orioli IM, Hecht JT, Buxó CJ, Butali A, Adeyemo WL, et al. Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions. Frontiers in Cell and Developmental Biology. 9: 621482. PMID 33898419 DOI: 10.3389/fcell.2021.621482 |
0.283 |
|
| 2011 |
Nielsen SM, Rubinstein WS, Thull DL, Armstrong MJ, Feingold E, Stang MT, Gnarra JR, Carty SE. Genotype-phenotype correlations of pheochromocytoma in two large von Hippel-Lindau (VHL) type 2A kindreds with different missense mutations. American Journal of Medical Genetics. Part A. 155: 168-73. PMID 21204227 DOI: 10.1002/Ajmg.A.33760 |
0.282 |
|
| 2017 |
Rosenthal SL, Demirci FY, Bamne MN, Kamboh MI, Lopez OL, Yan Q, Feingold E. [P1-160]: TARGETED SEQUENCING OF GWAS-IMPLICATED LOCI IN ALZHEIMER's DISEASE Alzheimer's & Dementia. 13: P304-P304. DOI: 10.1016/J.Jalz.2017.06.227 |
0.281 |
|
| 2005 |
Szatkiewicz JP, Feingold E. QTL mapping with discordant and concordant sibling pairs: new statistics and new design strategies. Genetic Epidemiology. 28: 326-40. PMID 15662636 DOI: 10.1002/Gepi.20065 |
0.278 |
|
| 2007 |
Brock GN, Weeks DE, Sobel E, Feingold E. A hierarchical model for estimating significance levels of non-parametric linkage statistics for large pedigrees. Genetic Epidemiology. 31: 417-30. PMID 17508354 DOI: 10.1002/Gepi.20222 |
0.278 |
|
| 2020 |
Faramawi MF, Orloff MS, Delongchamp R, Wang Y, Feingold E, Thapa S, Jin J, Delhey L, Abouelenein S, Zhang Q, Singh KP. Biological Pathways of Long-Term Visit-to-Visit Blood Pressure Variability in the American Population: Cardiovascular Health Study and Women’s Health Initiatives Biomed Research International. 2020: 1-7. DOI: 10.1155/2020/3841945 |
0.278 |
|
| 2015 |
Ray A, Hong CS, Feingold E, Ghosh P, Ghosh P, Bhaumik P, Dey S, Ghosh S. Maternal Telomere Length and Risk of Down Syndrome: Epidemiological Impact of Smokeless Chewing Tobacco and Oral Contraceptive on Segregation of Chromosome 21. Public Health Genomics. PMID 26439854 DOI: 10.1159/000439245 |
0.277 |
|
| 1995 |
Griffin DK, Abruzzo MA, Millie EA, Sheean LA, Feingold E, Sherman SL, Hassold TJ. Non-disjunction in human sperm: Evidence for an effect of increasing paternal age Human Molecular Genetics. 4: 2227-2232. PMID 8634691 DOI: 10.1093/Hmg/4.12.2227 |
0.276 |
|
| 2013 |
Herazo-Maya JD, Noth I, Duncan SR, Kim S, Ma SF, Tseng GC, Feingold E, Juan-Guardela BM, Richards TJ, Lussier Y, Huang Y, Vij R, Lindell KO, Xue J, Gibson KF, et al. Peripheral blood mononuclear cell gene expression profiles predict poor outcome in idiopathic pulmonary fibrosis. Science Translational Medicine. 5: 205ra136. PMID 24089408 DOI: 10.1126/Scitranslmed.3005964 |
0.273 |
|
| 2020 |
White JD, Indencleef K, Naqvi S, Eller RJ, Hoskens H, Roosenboom J, Lee MK, Li J, Mohammed J, Richmond S, Quillen EE, Norton HL, Feingold E, Swigut T, Marazita ML, et al. Insights into the genetic architecture of the human face. Nature Genetics. PMID 33288918 DOI: 10.1038/s41588-020-00741-7 |
0.271 |
|
| 2007 |
Mahony S, Corcoran DL, Feingold E, Benos PV. Regulatory conservation of protein coding and microRNA genes in vertebrates: lessons from the opossum genome. Genome Biology. 8: R84. PMID 17506886 DOI: 10.1186/Gb-2007-8-5-R84 |
0.269 |
|
| 2000 |
Feingold E, Brown AS, Sherman SL. Multipoint estimation of genetic maps for human trisomies with one parent or other partial data. American Journal of Human Genetics. 66: 958-68. PMID 10712210 DOI: 10.1086/302799 |
0.268 |
|
| 1995 |
Feingold E, Lamb NE, Sherman SL. Methods for genetic linkage analysis using trisomies American Journal of Human Genetics. 56: 475-483. PMID 7847384 |
0.268 |
|
| 2005 |
Corcoran DL, Feingold E, Dominick J, Wright M, Harnaha J, Trucco M, Giannoukakis N, Benos PV. Footer: a quantitative comparative genomics method for efficient recognition of cis-regulatory elements. Genome Research. 15: 840-7. PMID 15930494 DOI: 10.1101/Gr.2952005 |
0.267 |
|
| 2009 |
Iuliano AD, Feingold E, Wahed AS, Kleiner DE, Belle SH, Conjeevaram HS, Zmuda J, Liang TJ, Yee LJ. Host genetics, steatosis and insulin resistance among African Americans and Caucasian Americans with hepatitis C virus genotype-1 infection. Intervirology. 52: 49-56. PMID 19401628 DOI: 10.1159/000214380 |
0.266 |
|
| 2019 |
Rajakumar K, Yan Q, Khalid AT, Feingold E, Vallejo AN, Demirci FY, Kamboh MI. Gene Expression and Cardiometabolic Phenotypes of Vitamin D-Deficient Overweight and Obese Black Children. Nutrients. 11. PMID 31466225 DOI: 10.3390/Nu11092016 |
0.266 |
|
| 2019 |
Ju J, Tomaszewski EL, Orchard TJ, Evans RW, Feingold E, Costacou T. The haptoglobin 2-2 genotype is associated with cardiac autonomic neuropathy in type 1 diabetes: the RETRO HDLc study. Acta Diabetologica. PMID 31529337 DOI: 10.1007/S00592-019-01422-6 |
0.265 |
|
| 2007 |
Benos PV, Corcoran DL, Feingold E. Web-based identification of evolutionary conserved DNA cis-regulatory elements. Methods in Molecular Biology (Clifton, N.J.). 395: 425-36. PMID 17993689 DOI: 10.1007/978-1-59745-514-5_26 |
0.265 |
|
| 1998 |
Sun F, Ashley-Koch AE, Durham LK, Feingold E, Halloran ME, Manatunga AK, Sherman SL. Testing for contributions of mitochondrial DNA mutations to complex diseases Genetic Epidemiology. 15: 451-469. PMID 9728889 DOI: 10.1002/(Sici)1098-2272(1998)15:5<451::Aid-Gepi2>3.0.Co;2-3 |
0.262 |
|
| 2016 |
Oliver TR, Middlebrooks C, Harden A, Scott N, Johnson B, Jones J, Walker C, Wilkerson C, Saffold SH, Akinseye A, Smith T, Feingold E, Sherman SL. Variation in the Zinc Finger of PRDM9 is Associated with the Absence of Recombination along Nondisjoined Chromosomes 21 of Maternal Origin. Journal of Down Syndrome & Chromosome Abnormalities. 2. PMID 28702511 DOI: 10.4172/2472-1115.1000115 |
0.26 |
|
| 2012 |
Finegold DN, Baty CJ, Knickelbein KZ, Perschke S, Noon SE, Campbell D, Karlsson JM, Huang D, Kimak MA, Lawrence EC, Feingold E, Meriney SD, Brufsky AM, Ferrell RE. Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 2382-90. PMID 22351697 DOI: 10.1158/1078-0432.Ccr-11-2303 |
0.257 |
|
| 2018 |
Rosser TC, Edgin JO, Capone GT, Hamilton DR, Allen EG, Dooley KJ, Anand P, Strang JF, Armour AC, Frank-Crawford MA, Channell MM, Pierpont EI, Feingold E, Maslen CL, Reeves RH, et al. Associations Between Medical History, Cognition, and Behavior in Youth With Down Syndrome: A Report From the Down Syndrome Cognition Project. American Journal On Intellectual and Developmental Disabilities. 123: 514-528. PMID 30421968 DOI: 10.1352/1944-7558-123.6.514 |
0.256 |
|
| 2021 |
Liu D, Ban HJ, El Sergani AM, Lee MK, Hecht JT, Wehby GL, Moreno LM, Feingold E, Marazita ML, Cha S, Szabo-Rogers HL, Weinberg SM, Shaffer JR. × Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Frontiers in Genetics. 12: 674642. PMID 34434215 DOI: 10.3389/fgene.2021.674642 |
0.255 |
|
| 2015 |
Shaffer JR, Leslie EJ, Feingold E, Govil M, McNeil DW, Crout RJ, Weyant RJ, Marazita ML. Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia. International Journal of Dentistry. 2015: 938213. PMID 26106416 DOI: 10.1155/2015/938213 |
0.252 |
|
| 2021 |
Liu D, Alhazmi N, Matthews H, Lee MK, Li J, Hecht JT, Wehby GL, Moreno LM, Heike CL, Roosenboom J, Feingold E, Marazita ML, Claes P, Liao EC, Weinberg SM, et al. Impact of low-frequency coding variants on human facial shape. Scientific Reports. 11: 748. PMID 33436952 DOI: 10.1038/s41598-020-80661-y |
0.252 |
|
| 2007 |
Sengul H, Bhattacharjee S, Feingold E, Weeks DE. The elusive goal of pedigree weights. Genetic Epidemiology. 31: 51-65. PMID 17086515 DOI: 10.1002/Gepi.20188 |
0.252 |
|
| 2014 |
Weinreb NJ, Feingold E, Shankar S, Rosenbloom BE, Finegold D. Evaluation of Disease Burden and Response to Treatment in Adults with Type 1 Gaucher Disase Using a Validated DS3 Severity Score Index Blood. 124: 4957-4957. DOI: 10.1182/Blood.V124.21.4957.4957 |
0.251 |
|
| 2023 |
Zou T, Neiswanger K, Feingold E, Foxman B, McNeil DW, Marazita ML, Shaffer JR. Potential risk factors and genetic variants associated with dental caries incidence in Appalachia using genome-wide survival analysis. International Journal of Molecular Epidemiology and Genetics. 14: 19-33. PMID 37736056 |
0.248 |
|
| 2013 |
Shaffer JR, Feingold E, Wang X, Weeks DE, Weyant RJ, Crout R, McNeil DW, Marazita ML. Clustering tooth surfaces into biologically informative caries outcomes. Journal of Dental Research. 92: 32-7. PMID 23064960 DOI: 10.1177/0022034512463241 |
0.248 |
|
| 2022 |
Li J, Glover JD, Zhang H, Peng M, Tan J, Mallick CB, Hou D, Yang Y, Wu S, Liu Y, Peng Q, Zheng SC, Crosse EI, Medvinsky A, Anderson RA, ... ... Feingold E, et al. Limb development genes underlie variation in human fingerprint patterns. Cell. 185: 95-112.e18. PMID 34995520 DOI: 10.1016/j.cell.2021.12.008 |
0.246 |
|
| 2010 |
Ferrell RE, Baty CJ, Kimak MA, Karlsson JM, Lawrence EC, Franke-Snyder M, Meriney SD, Feingold E, Finegold DN. GJC2 missense mutations cause human lymphedema. American Journal of Human Genetics. 86: 943-8. PMID 20537300 DOI: 10.1016/J.Ajhg.2010.04.010 |
0.245 |
|
| 2002 |
Jiang Z, Feingold E, Kochanek S, Clemens PR. Systemic delivery of a high-capacity adenoviral vector expressing mouse CTLA4Ig improves skeletal muscle gene therapy. Molecular Therapy : the Journal of the American Society of Gene Therapy. 6: 369-76. PMID 12231173 DOI: 10.1006/Mthe.2002.0676 |
0.244 |
|
| 2022 |
Carlson JC, Shaffer JR, Deleyiannis F, Hecht JT, Wehby GL, Christensen K, Feingold E, Weinberg SM, Marazita ML, Leslie EJ. Genome-wide Interaction Study Implicates and Alcohol Exposure and and Smoking in Orofacial Cleft Risk. Frontiers in Cell and Developmental Biology. 10: 621261. PMID 35223824 DOI: 10.3389/fcell.2022.621261 |
0.244 |
|
| 1997 |
Feingold E, Siegmund DO. Strategies for mapping heterogeneous recessive traits by allele-sharing methods American Journal of Human Genetics. 60: 965-978. PMID 9106544 |
0.242 |
|
| 2001 |
Jiang ZL, Reay D, Kreppel F, Gambotto A, Feingold E, Kochanek S, McCarthy SA, Clemens PR. Local high-capacity adenovirus-mediated mCTLA4Ig and mCD40Ig expression prolongs recombinant gene expression in skeletal muscle. Molecular Therapy : the Journal of the American Society of Gene Therapy. 3: 892-900. PMID 11407903 DOI: 10.1006/Mthe.2001.0331 |
0.24 |
|
| 2014 |
Qutub K, Lacomis D, Albert SM, Feingold E. Life factors affecting depression and burden in amyotrophic lateral sclerosis caregivers. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 15: 292-7. PMID 24555470 DOI: 10.3109/21678421.2014.886699 |
0.237 |
|
| 2021 |
Sabiha B, Bhatti A, Fan KH, John P, Muaaz Aslam M, Ali J, Feingold E, Yesim Demirci F, Ilyas Kamboh M. Assessment of genetic risk of type 2 diabetes among Pakistanis based on GWAS-implicated loci. Gene. 145563. PMID 33705809 DOI: 10.1016/j.gene.2021.145563 |
0.237 |
|
| 2019 |
Chen M, Wright CD, Tokede O, Yansane A, Montasem A, Kalenderian E, Beaty TH, Feingold E, Shaffer JR, Crout RJ, Neiswanger K, Weyant RJ, Marazita ML, McNeil DW. Predictors of dental care utilization in north-central Appalachia in the USA. Community Dentistry and Oral Epidemiology. PMID 30993747 DOI: 10.1111/Cdoe.12453 |
0.234 |
|
| 2020 |
Samuels BD, Aho R, Brinkley JF, Bugacov A, Feingold E, Fisher S, Gonzalez-Reiche AS, Hacia JG, Hallgrimsson B, Hansen K, Harris MP, Ho TV, Holmes G, Hooper JE, Jabs EW, et al. FaceBase 3: analytical tools and FAIR resources for craniofacial and dental research. Development (Cambridge, England). 147. PMID 32958507 DOI: 10.1242/Dev.191213 |
0.232 |
|
| 2009 |
Henson BJ, Bhattacharjee S, O'Dee DM, Feingold E, Gollin SM. Decreased expression of miR-125b and miR-100 in oral cancer cells contributes to malignancy. Genes, Chromosomes & Cancer. 48: 569-82. PMID 19396866 DOI: 10.1002/Gcc.20666 |
0.231 |
|
| 2015 |
Weinreb NJ, Finegold DN, Feingold E, Zeng Z, Rosenbloom BE, Shankar SP, Amato D. Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3). Orphanet Journal of Rare Diseases. 10: 64. PMID 25994334 DOI: 10.1186/S13023-015-0280-3 |
0.23 |
|
| 2005 |
Katsiaras A, Newman AB, Kriska A, Brach J, Krishnaswami S, Feingold E, Kritchevsky SB, Li R, Harris TB, Schwartz A, Goodpaster BH. Skeletal muscle fatigue, strength, and quality in the elderly: the Health ABC Study. Journal of Applied Physiology (Bethesda, Md. : 1985). 99: 210-6. PMID 15718402 DOI: 10.1152/Japplphysiol.01276.2004 |
0.23 |
|
| 1996 |
Lamb NE, Feingold E, Sherman SL. Statistical models for trisomic phenotypes American Journal of Human Genetics. 58: 201-212. PMID 8554057 |
0.229 |
|
| 2005 |
Corcoran DL, Feingold E, Benos PV. FOOTER: a web tool for finding mammalian DNA regulatory regions using phylogenetic footprinting. Nucleic Acids Research. 33: W442-6. PMID 15980508 DOI: 10.1093/Nar/Gki420 |
0.229 |
|
| 2023 |
Diaz Perez KK, Curtis SW, Sanchis-Juan A, Zhao X, Head T, Ho S, Carter B, McHenry T, Bishop MR, Valencia-Ramirez LC, Restrepo C, Hecht JT, Uribe LM, Wehby G, Weinberg SM, ... ... Feingold E, et al. Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100918. PMID 37330696 DOI: 10.1016/j.gim.2023.100918 |
0.227 |
|
| 2006 |
Schaefer TM, Fuller CL, Basu S, Fallert BA, Poveda SL, Sanghavi SK, Choi YK, Kirschner DE, Feingold E, Reinhart TA. Increased expression of interferon-inducible genes in macaque lung tissues during simian immunodeficiency virus infection. Microbes and Infection / Institut Pasteur. 8: 1839-50. PMID 16822691 DOI: 10.1016/J.Micinf.2006.02.022 |
0.226 |
|
| 1993 |
Feingold E, Brown PO, Siegmund D. Gaussian models for genetic linkage analysis using complete high- resolution maps of identity by descent American Journal of Human Genetics. 53: 234-251. PMID 8317489 |
0.223 |
|
| 2010 |
Thomas CR, Glover KZ, Wilson JW, Feingold E, Constantino JP. Abstract B116: Comparison of African American (AA) and Caucasian patients with respect to radiotherapy (RT) delivery in National Surgical Adjuvant Breast & Bowel Project (NSABP) breast cancer treatment trials Cancer Epidemiology, Biomarkers & Prevention. 19. DOI: 10.1158/1055-9965.Disp-10-B116 |
0.221 |
|
| 1997 |
Cope TC, Sokoloff AJ, Dacko SM, Huot R, Feingold E. Stability of motor-unit force thresholds in the decerebrate cat. Journal of Neurophysiology. 78: 3077-82. PMID 9405527 DOI: 10.1152/Jn.1997.78.6.3077 |
0.221 |
|
| 2014 |
Redig JK, Fouad GT, Babcock D, Reshey B, Feingold E, Reeves RH, Maslen CL. Allelic Interaction between CRELD1 and VEGFA in the Pathogenesis of Cardiac Atrioventricular Septal Defects. Aims Genetics. 1: 1-19. PMID 25328912 DOI: 10.3934/genet.2014.1.1#sthash.jksuJTeC.dpuf |
0.22 |
|
| 2023 |
Aslam MM, Fan KH, Lawrence E, Bedison MA, Snitz BE, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Genome-wide analysis identifies novel loci influencing plasma apolipoprotein E concentration and Alzheimer's disease risk. Molecular Psychiatry. PMID 37666928 DOI: 10.1038/s41380-023-02170-4 |
0.216 |
|
| 2022 |
Fan K, Francis L, Aslam MM, Bedison MA, Lawrence E, Acharya V, Snitz BE, Ganguli M, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Investigation of the independent role of a rare APOE variant (L28P; APOE*4Pittsburgh) in late-onset Alzheimer disease. Neurobiology of Aging. 122: 107-111. PMID 36528961 DOI: 10.1016/j.neurobiolaging.2022.11.007 |
0.215 |
|
| 2017 |
Randall CL, Wright CD, Chernus JM, McNeil DW, Feingold E, Crout RJ, Neiswanger K, Weyant RJ, Shaffer JR, Marazita ML. A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain. Pain Research & Management. 2017: 7375468. PMID 28701861 DOI: 10.1155/2017/7375468 |
0.215 |
|
| 2007 |
Baca JT, Taormina CR, Feingold E, Finegold DN, Grabowski JJ, Asher SA. Mass spectral determination of fasting tear glucose concentrations in nondiabetic volunteers. Clinical Chemistry. 53: 1370-2. PMID 17495022 DOI: 10.1373/Clinchem.2006.078543 |
0.211 |
|
| 2022 |
Harper JD, Fan KH, Aslam MM, Snitz BE, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Journal of Alzheimer's Disease : Jad. PMID 35694926 DOI: 10.3233/JAD-220293 |
0.208 |
|
| 1997 |
Lamb NE, Feingold E, Sherman SL. Estimating meiotic exchange patterns from recombination data: An application to humans Genetics. 146: 1011-1017. PMID 9215904 |
0.206 |
|
| 2010 |
Thomas CR, Glover KZ, Constantino JP, Feingold E, Wilson JW. Comparison of African American (AA) and White (W) Patients with Respect to Radiotherapy (RT) Delivery in National Surgical Adjuvant Breast and Bowel Project (NSABP) Breast Cancer Treatment Trials International Journal of Radiation Oncology Biology Physics. 78. DOI: 10.1016/J.Ijrobp.2010.07.066 |
0.193 |
|
| 2021 |
Curtis SW, Chang D, Sun MR, Epstein MP, Murray JC, Feingold E, Beaty TH, Weinberg SM, Marazita ML, Lipinski RJ, Carlson JC, Leslie EJ. FAT4 identified as a potential modifier of orofacial cleft laterality. Genetic Epidemiology. PMID 34130359 DOI: 10.1002/gepi.22420 |
0.187 |
|
| 2018 |
Delongchamp R, Faramawi MF, Feingold E, Chung D, Abouelenein S. The Association between SNPs and a Quantitative Trait: Power Calculation. European Journal of Environment and Public Health. 2. PMID 31259311 DOI: 10.20897/ejeph/3925 |
0.187 |
|
| 2021 |
Zhang W, Venkataraghavan S, Hetmanski JB, Leslie EJ, Marazita ML, Feingold E, Weinberg SM, Ruczinski I, Taub MA, Scott AF, Ray D, Beaty TH. Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Frontiers in Cell and Developmental Biology. 9: 621018. PMID 33937227 DOI: 10.3389/fcell.2021.621018 |
0.179 |
|
| 2010 |
Park WG, Barmada MM, Feingold E, Wang X, Wu K, Zhao Y, Gao Z, Vantini I, Chari ST, Fernández-Zapico ME, Hornum M, Pedersen JF, Larsen S, Olsen O, Holst JJ, et al. IAP Membership Application Form 2010 Pancreatology. 10: 410-410. DOI: 10.1159/000316048 |
0.176 |
|
| 2003 |
Szatkiewicz JP, T Cuenco K, Feingold E. Recent advances in human quantitative-trait-locus mapping: comparison of methods for discordant sibling pairs. American Journal of Human Genetics. 73: 874-85. PMID 12970846 DOI: 10.1086/378590 |
0.174 |
|
| 2020 |
Aslam MM, John P, Fan KH, Bhatti A, Feingold E, Demirci FY, Kamboh MI. Association of Gene Copy Number Variation and Rheumatoid Arthritis Susceptibility. Disease Markers. 2020: 7189626. PMID 33101545 DOI: 10.1155/2020/7189626 |
0.171 |
|
| 2022 |
Aslam MM, John P, Fan KH, Malik JM, Feingold E, Demirci FY, Kamboh MI. Association of Fc Gamma Receptor 3B Gene Copy Number Variation with Rheumatoid Arthritis Susceptibility. Genes. 13. PMID 36553504 DOI: 10.3390/genes13122238 |
0.171 |
|
| 1989 |
Feingold EA, Forget BG. The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the β-globin gene cluster Blood. 74: 2178-2186. PMID 2478223 |
0.164 |
|
| 2012 |
Tseng GC, Ghosh D, Feingold E. Comprehensive literature review and statistical considerations for microarray meta-analysis. Nucleic Acids Research. 40: 3785-99. PMID 22262733 DOI: 10.1093/nar/gkr1265 |
0.158 |
|
| 1996 |
Nolin SL, Lewis FA, Ye LL, Houck GE, Glicksman AE, Limprasert P, Li SY, Zhong N, Ashley AE, Feingold E, Sherman SL, Ted Brown W. Familial transmission of the FMR1 CGG repeat American Journal of Human Genetics. 59: 1252-1261. PMID 8940270 |
0.157 |
|
| 1983 |
Tuan D, Feingold E, Newman M, Weissman SM, Forget BG. Different 3' end points of deletions causing δβ-thalassemia and hereditary persistence of fetal hemoglobin: Implications for the control of γ-globin gene expression in man Proceedings of the National Academy of Sciences of the United States of America. 80: 6937-6941. PMID 6196781 DOI: 10.1073/Pnas.80.22.6937 |
0.152 |
|
| 2015 |
Ray A, Hong CS, Feingold E, Ghosh P, Bhaumik P, Dey S, Ghosh S. Maternal Telomere Length and Risk of Down Syndrome: Epidemiological Impact of Smokeless Chewing Tobacco and Oral Contraceptive on Segregation of Chromosome 21 Public Health Genomics. DOI: 10.1159/000439245 |
0.146 |
|
| 2023 |
Gorijala P, Aslam MM, Dang LT, Xicota L, Fernandez MV, Sung YJ, Fan KH, Feingold E, Surace EI, Chhatwal JP, Hom CL, Hartley SL, Hassenstab J, Perrin RJ, Mapstone M, et al. Alzheimer's polygenic risk scores are associated with cognitive phenotypes in Down syndrome. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37855447 DOI: 10.1002/alz.13506 |
0.143 |
|
| 1999 |
Feingold EA, Penny LA, Nienhuis AW, Forget BG. An olfactory receptor gene is located in the extended human beta-globin gene cluster and is expressed in erythroid cells. Genomics. 61: 15-23. PMID 10512676 DOI: 10.1006/Geno.1999.5935 |
0.138 |
|
| 1985 |
Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Analysis of mutations associated with deletion and nondeletion hereditary persistence of fetal hemoglobin Progress in Clinical and Biological Research. 191: 107-124. PMID 2413468 |
0.126 |
|
| 1996 |
Griffin DK, Abruzzo MA, Millie EA, Feingold E, Hassold TJ. Sex ratio in normal and disomic sperm: evidence that the extra chromosome 21 preferentially segregates with the Y chromosome. American Journal of Human Genetics. 59: 1108-13. PMID 8900240 |
0.126 |
|
| 2023 |
Miller RG, Mychaleckyj JC, Onengut-Gumuscu S, Feingold E, Orchard TJ, Costacou T. DNA methylation and 28-year cardiovascular disease risk in type 1 diabetes: the Epidemiology of Diabetes Complications (EDC) cohort study. Clinical Epigenetics. 15: 122. PMID 37533055 DOI: 10.1186/s13148-023-01539-0 |
0.11 |
|
| 2023 |
Acharya V, Fan KH, Snitz BE, Ganguli M, DeKosky ST, Lopez OL, Feingold E, Kamboh MI. Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 37089073 DOI: 10.1002/alz.13064 |
0.108 |
|
| 1975 |
Solish G, Feingold E, Harper RG. Chromosomal studies of methadone maintained women and their newborns Pediatric Research. 9. |
0.102 |
|
| 1999 |
Strausberg RL, Feingold EA, Klausner RD, Collins FS. The mammalian gene collection. Science (New York, N.Y.). 286: 455-7. PMID 10521335 DOI: 10.1126/Science.286.5439.455 |
0.1 |
|
| 2000 |
Redfern RO, Horii SC, Feingold E, Kundel HL. Radiology workflow and patient volume: Effect of picture archiving and communication systems on technologists and radiologists Journal of Digital Imaging. 13: 97-100. PMID 10847373 |
0.096 |
|
| 1990 |
Feingold E, Werby E. Supporting the independence of elderly residents through control over their environment Journal of Housing For the Elderly. 6: 25-32. DOI: 10.1300/J081V06N01_02 |
0.092 |
|
| 2020 |
Zhou Y, Cuddy R, McNeil DW, Wright CD, Crout RJ, Feingold E, Neiswanger K, Marazita ML, Shaffer JR. Oral health and related risk indicators in north-central Appalachia differ by rurality. Community Dentistry and Oral Epidemiology. PMID 33368457 DOI: 10.1111/cdoe.12618 |
0.089 |
|
| 1977 |
Harper RG, Solish G, Feingold E, Gersten-Woolf NB, Sokal MM. Maternal ingested methadone, body fluid methadone, and the neonatal withdrawal syndrome American Journal of Obstetrics and Gynecology. 129: 417-424. PMID 910821 |
0.08 |
|
| 1985 |
Feingold EA, Collins FS, Metherall JE, Stoeckert CJ, Weissman SM, Forget BG. Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia. Annals of the New York Academy of Sciences. 445: 159-69. PMID 2409868 DOI: 10.1111/J.1749-6632.1985.Tb17185.X |
0.076 |
|
| 2001 |
Horii S, Redfern R, Feingold E, Kundel H, Nodine C, Arnold D, Abbuhl S, Lowe R, Brikman I. An automated results notification system for PACS. Journal of Digital Imaging. 14: 192-8. PMID 11894892 DOI: 10.1007/s10278-001-0105-x |
0.073 |
|
| 1994 |
Feingold E, Wasser J. Walk-through surveys for child labor American Journal of Industrial Medicine. 26: 803-807. PMID 7892831 |
0.071 |
|
| 1998 |
Langlotz CP, Pratt HM, Feingold ER, Horii SC, Kundel HL. Factors influencing the adoption of digital imaging systems Proceedings of Spie - the International Society For Optical Engineering. 3339: 421-428. DOI: 10.1117/12.319796 |
0.068 |
|
| 2002 |
Feingold E, Sheir-Neiss G, Melnychuk J, Bachrach S, Paul D. Eating disorder symptomatology is not associated with pregnancy and perinatal complications in a cohort of adolescents who were born preterm. The International Journal of Eating Disorders. 31: 202-9. PMID 11920981 DOI: 10.1002/Eat.10021 |
0.065 |
|
| 1993 |
Evans MI, Gleicher E, Feingold E, Johnson MP, Sokol RJ. The fiscal impact of the medicaid abortion funding ban in Michigan Obstetrics and Gynecology. 82: 555-560. PMID 8135922 |
0.061 |
|
| 1983 |
Classen W, Feingold E, Better P. Influence of sensory suggestibility on treatment outcome in headache patients Neuropsychobiology. 10: 44-47. PMID 6657038 DOI: 10.1159/000117982 |
0.06 |
|
| 2015 |
Shaffer JR, Leslie EJ, Feingold E, Govil M, McNeil DW, Crout RJ, Weyant RJ, Marazita ML. Caries Experience Differs between Females and Males across Age Groups in Northern Appalachia International Journal of Dentistry. 2015. DOI: 10.1155/2015/938213 |
0.055 |
|
| 1969 |
Walford RL, Troup GM, Zeller E, Shanbrom E, Feingold E. The "Thompson" specificity and the HL-A human leukocyte system. Proceedings of the Society For Experimental Biology and Medicine. Society For Experimental Biology and Medicine (New York, N.Y.). 131: 478-81. PMID 5787128 DOI: 10.3181/00379727-131-33906 |
0.055 |
|
| 2003 |
Feingold EK, Whitney CG, Elliott J, Schwartzman JD. The outbreak of conjunctivitis at Dartmouth [2] (multiple letters) New England Journal of Medicine. 348: 2577-2578. DOI: 10.1056/NEJM200306193482517 |
0.053 |
|
| 2002 |
Feingold E, Sheir-Neiss G, Melnychuk J, Bachrach S, Paul D. HRQL and severity of brain ultrasound findings in a cohort of adolescents who were born preterm. The Journal of Adolescent Health : Official Publication of the Society For Adolescent Medicine. 31: 234-9. PMID 12225735 DOI: 10.1016/S1054-139X(01)00407-4 |
0.048 |
|
| 2014 |
Jarosz PA, Davis JE, Yarandi HN, Farkas R, Feingold E, Shippings SH, Smith AL, Williams D. Obesity in urban women: associations with sleep and sleepiness, fatigue and activity. Women's Health Issues : Official Publication of the Jacobs Institute of Women's Health. 24: e447-54. PMID 24981402 DOI: 10.1016/J.Whi.2014.04.005 |
0.048 |
|
| 1996 |
Shile PE, Kundel HL, Seshadri SB, Carey B, Kishore S, Brikman I, Feingold E, Lanken PN, Purcell JA. Factors affecting the electronic communication of radiological information to an intensive-care unit. Journal of Telemedicine and Telecare. 2: 199-204. PMID 9375059 DOI: 10.1258/1357633961930077 |
0.047 |
|
| 1979 |
Zauderer B, Coppa AP, Noone MJ, DeDominicis L, Gatti A, Rogers DA, Feingold E, Faust B. DEVELOPMENTS IN ELECTRODES AND POWER CONDITIONING SYSTEMS FOR OPEN-CYCLE MHD GENERATORS . |
0.045 |
|
| 1996 |
Kundel HL, Seshadri SB, Langlotz CP, Lanken PN, Horii SC, Nodine CF, Polansky M, Feingold E, Brikman I, Bozzo M, Redfern R. Prospective study of a PACS: Information flow and clinical action in a medical intensive care unit Radiology. 199: 143-149. PMID 8633138 DOI: 10.1148/RADIOLOGY.199.1.8633138 |
0.044 |
|
| 1994 |
Seshadri SB, Arenson RL, Kundel HL, Feingold E, Kishore S, Horii SC, Stevens JF, Lanken PN. High-resolution image workstation for intensive care units. Radiographics : a Review Publication of the Radiological Society of North America, Inc. 14: 863-73. PMID 7938773 DOI: 10.1148/Radiographics.14.4.7938773 |
0.04 |
|
| 1977 |
Harper RG, Solish G, Feingold E. Predictors of the severity of neonatal methadone withdrawal Pediatric Research. 11. |
0.039 |
|
| 1974 |
Pochedly C, Mehta A, Feingold E. Priapism with hyperacute stem cell leukemia New York State Journal of Medicine. 74: 540-541. PMID 4522659 |
0.038 |
|
| 1978 |
Feingold E, Chemnitz G. New studies of suggestibility and relations with medical-psychological research Medizinische Psychologie Lehre Forschung Und Klinik. 4: 245-246. |
0.038 |
|
| 1987 |
Feingold E. Solomon J. Axelrod, M.D., M.P.H., 1912-87 Medical Care Research and Review. 44: 407-408. DOI: 10.1177/107755878704400209 |
0.037 |
|
| 2015 |
Feingold E, Adams J, Penprase B, Tubie B. Effect of body mass index and albumin on mortality rates for adult African-American hemodialysis patients. Journal of the American Association of Nurse Practitioners. 27: 637-45. PMID 25761048 DOI: 10.1002/2327-6924.12236 |
0.037 |
|
| 1985 |
Chu CL, Seshadri SB, Feingold E, Tretiak OJ. LOW-COST IMAGE PROCESSING SYSTEM . 93-97. |
0.036 |
|
| 1983 |
Forget BG, Tuan D, Newman MV, Feingold EA, Collins F, Fukumaki Y, Jagadeeswaran P, Weissman SM. Molecular studies of mutations that increase Hb F production in man Progress in Clinical and Biological Research. 134: 65-76. PMID 6198666 |
0.035 |
|
| 1998 |
Lee PR, Elders MJ, McGinnis JM, Satcher D, Clinton JJ, Kessler DA, Robinson WA, Lincoln ME, Varmus H, Johnson EM, Feingold E, Ibrahim M, Mahan CS, Mullet ME, Mecca A, et al. Health care reform and public health: A paper on population-based core functions: The core functions project, U.S. public health service, 1993 Journal of Public Health Policy. 19: 394-419. PMID 9922618 DOI: 10.2307/3343074 |
0.034 |
|
| 1988 |
Feingold E. In memoriam. Solomon Jacob Axelrod, MD, MPH, September 25, 1912-September 21, 1987 Medical Care. 26: 643-644. PMID 3288819 |
0.032 |
|
| 1985 |
Musikant S, Samanta SC, Feingold E. TRANSFORMATION TOUGHENED CERAMICS FOR THE HEAVY DUTY DIESEL ENGINE TECHNOLOGY PROGRAM Proceedings - Society of Automotive Engineers. 487-496. |
0.031 |
|
| 1998 |
Shrestha SK, Mezrich RS, Kundel HL, Feingold ER, Horii SC, Khalsa SS. Experience with integrating a filmless PACS into an emergency department Proceedings of Spie - the International Society For Optical Engineering. 3339: 479-487. DOI: 10.1117/12.319804 |
0.029 |
|
| 2003 |
Feingold EK. The outbreak of conjunctivitis at Dartmouth The New England Journal of Medicine. 348. PMID 12815147 |
0.028 |
|
| 1975 |
Harindranath A, Feingold E, Sokal M. Cellular content of placentas of methadone maintained addicts Pediatric Research. 9. |
0.026 |
|
| 1985 |
Miller SA, Feingold E, Vining CB. APPLICATION OF GAS ATOMIZED POWDER FOR IMPROVED THERMOELECTRIC DEVICES Modern Developments in Powder Metallurgy. 17: 671-682. |
0.025 |
|
| 1980 |
Chemnitz G, Feingold E. A report on the development and prospects of Medical Psychology in the Federal Republic of Germany Metamedicine. 1: 369-374. DOI: 10.1007/BF00882623 |
0.024 |
|
| 1989 |
Kishore S, Feingold E. Designing a flexible user interface for both users and programmers. Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society. 13: 105-13. PMID 2924281 DOI: 10.1016/0895-6111(89)90082-7 |
0.024 |
|
| 1996 |
Feingold E. CREF must get rid of its tobacco-related investments Chronicle of Higher Education. 43. |
0.023 |
|
| 1958 |
Feingold E. 13. Reviews: Government Sponsored and Government Supported Research: Social Sciences and Interdisciplinary Areas: National Science Foundation (Washington, D. C.: National Science Foundation, March 1958. Multilithed American Behavioral Scientist. 1: 40. DOI: 10.1177/000276425800100613 |
0.023 |
|
| 1998 |
Pratt HM, Langlotz CP, Feingold ER, Schwartz JS, Kundel HL. Incremental cost of department-wide implementation of a picture archiving and communication system and computed radiography. Radiology. 206: 245-52. PMID 9423679 DOI: 10.1148/radiology.206.1.9423679 |
0.023 |
|
| 1982 |
Feingold E, Classen W, Tille C, Netter P. Comparison of analgesics on different pain stimuli Arzneimittel-Forschung/Drug Research. 32: 901. |
0.022 |
|
| 1983 |
Feingold E. The new politics of national health insurance Journal of Health and Human Resources Administration. 5: 266-279. PMID 10259530 |
0.022 |
|
| 1998 |
Feingold E. Public health versus civil liberties Public Health Reports. 113: 334-335. PMID 9672572 |
0.02 |
|
| 1970 |
Feingold E. A political scientist’s view of the neighborhood health center as a new social institution Medical Care. 8: 108-115. PMID 5467699 |
0.02 |
|
| 1979 |
Feingold E, Chemnitz G. The curriculum in medical psychology of the University of Mainz Medizinische Psychologie Lehre Forschung Und Klinik. 5: 160-168. |
0.02 |
|
| 1975 |
Harper RG, Feingold E, Solish G, Sokal M. Heat-stable alkaline phosphatase in methadone-maintained pregnancies Addictive Diseases. 2: 89-99. PMID 1163376 |
0.02 |
|
| 1994 |
Feingold E. Health care reform - More than cost containment and universal access American Journal of Public Health. 84: 727-728. PMID 8179038 |
0.017 |
|
| 1969 |
Shepherd LP, Feingold E, Shanbrom E. An unusual occurrence of anti-Xg-a Vox Sanguinis. 16: 157-160. PMID 4179781 |
0.016 |
|
| 1995 |
Feingold E. The defeat of health care reform: Misplaced mistrust in government American Journal of Public Health. 85: 1619-1622. PMID 7503334 |
0.016 |
|
| 1968 |
Shanbrom E, Feingold E, Shepherd L, Walford RL. Antisera for tissue-typing: the production of cytotoxic and agglutinating antibodies following intradermal leukocyte injections in man Blood. 32: 402-411. PMID 5675978 |
0.015 |
|
| 1962 |
Feingold E. Discussions and Reviews : Nuclear attack and civil defense: A review Journal of Conflict Resolution. 6: 282-289. DOI: 10.1177/002200276200600310 |
0.014 |
|
| 1985 |
Classen W, Feingold E. Use of placebos in medical practice Pharmacopsychiatry. 18: 131-132. |
0.014 |
|
| 1993 |
Feingold E. Kids Are Working American Journal of Diseases of Children. 147: 929-931. PMID 8362800 DOI: 10.1001/archpedi.1993.02160330019004 |
0.013 |
|
| 1988 |
Feingold E, Wegman ME. Solomon Jacob Axelrod, MD, MPH, national leader in medical care organization (September 25, 1912-September 21, 1987) American Journal of Public Health. 78: 324. PMID 3277455 |
0.012 |
|
| 1969 |
Feingold E. The politics of health planning. 3. The changing political character of health planning American Journal of Public Health and the Nation"S Health. 59: 803-808. PMID 5813921 |
0.01 |
|
| 1991 |
Anthony AS, McInnis B, McPherson J, Moseley N, Forsberg D, Maguire A, Feingold E, Mitchell D. The homeless elderly Pride Institute Journal of Long Term Home Health Care. 10: 6-15. PMID 10116049 |
0.01 |
|
| 2010 |
Kuo CL, Feingold E. Letter to the Editor Genetic Epidemiology. 34: 772-772. DOI: 10.1002/gepi.20524 |
0.01 |
|
| 1988 |
Feingold E. What other states are doing about access Michigan Hospitals. 24. PMID 10287993 |
0.01 |
|
| 1984 |
Musikant S, Rauch HW, Feingold E. TRANSFORMATION TOUGHENING OF CERAMICS FOR ENGINES Proceedings - Society of Automotive Engineers. 215-222. |
0.01 |
|
| 1974 |
Brown RE, Feingold E, Levin H. The citizentry and the hospital Abstracts of Hospital Management Studies. 11. |
0.01 |
|
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