| Year |
Citation |
Score |
| 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 |
0.309 |
|
| 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 |
0.304 |
|
| 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 |
0.331 |
|
| 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 |
0.331 |
|
| 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 |
0.355 |
|
| 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 |
0.394 |
|
| 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 |
0.338 |
|
| 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 |
0.423 |
|
| 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 |
0.4 |
|
| 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 |
0.383 |
|
| 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 |
0.36 |
|
| 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 |
0.332 |
|
| 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 |
0.387 |
|
| 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 |
0.396 |
|
| 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 |
0.343 |
|
| 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 |
0.39 |
|
| 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 |
0.318 |
|
| 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 |
0.372 |
|
| 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 |
0.399 |
|
| 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 |
0.382 |
|
| 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 |
0.335 |
|
| 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 |
0.386 |
|
| 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 |
0.407 |
|
| 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 |
0.359 |
|
| 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 |
0.328 |
|
| 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 |
0.403 |
|
| 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 |
0.424 |
|
| 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 |
0.381 |
|
| 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 |
0.331 |
|
| 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 |
0.433 |
|
| 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 |
0.415 |
|
| 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 |
0.364 |
|
| 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 |
0.342 |
|
| 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 |
0.43 |
|
| 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 |
0.384 |
|
| 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 |
0.32 |
|
| 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 |
0.325 |
|
| 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 |
0.418 |
|
| 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 |
0.429 |
|
| 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 |
0.423 |
|
| 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 |
0.428 |
|
| 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 |
0.34 |
|
| 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 |
0.4 |
|
| 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 |
0.399 |
|
| 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 |
0.413 |
|
| 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 |
0.392 |
|
| 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 |
0.375 |
|
| 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 |
0.386 |
|
| 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 |
0.319 |
|
| 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 |
0.389 |
|
| 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 |
0.381 |
|
| 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 |
0.396 |
|
| 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 |
0.308 |
|
| 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 |
0.362 |
|
| 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 |
0.413 |
|
| 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 |
0.383 |
|
| 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 |
0.433 |
|
| 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 |
0.301 |
|
| 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 |
0.354 |
|
| 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 |
0.31 |
|
| 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 |
0.378 |
|
| 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 |
0.334 |
|
| 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 |
0.406 |
|
| 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 |
0.406 |
|
| 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 |
0.333 |
|
| 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 |
0.356 |
|
| 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 |
0.314 |
|
| 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 |
0.413 |
|
| 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 |
0.353 |
|
| 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 |
0.348 |
|
| 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 |
0.321 |
|
| 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 |
0.314 |
|
| 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 |
0.335 |
|
| 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 |
0.338 |
|
| 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 |
0.413 |
|
| 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 |
0.331 |
|
| 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 |
0.317 |
|
| 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 |
0.413 |
|
| 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 |
0.408 |
|
| 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 |
0.365 |
|
| 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 |
0.389 |
|
| 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 |
0.341 |
|
| 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 |
0.315 |
|
| 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 |
0.416 |
|
| 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 |
0.397 |
|
| 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 |
0.325 |
|
| 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 |
0.386 |
|
| 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 |
0.413 |
|
| 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 |
0.415 |
|
| 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 |
0.407 |
|
| 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 |
0.305 |
|
| 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 |
0.353 |
|
| 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 |
0.361 |
|
| 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 |
0.306 |
|
| 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 |
0.332 |
|
| 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 |
0.363 |
|
| 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 |
0.371 |
|
| 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 |
0.313 |
|
| 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 |
0.313 |
|
| 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 |
0.362 |
|
| 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 |
0.305 |
|
| 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 |
0.414 |
|
| 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 |
0.341 |
|
| 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 |
0.315 |
|
| 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 |
0.643 |
|
| 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 |
0.313 |
|
| 2004 |
Broman KW, Feingold E. SNPs made routine. Nature Methods. 1: 104-5. PMID 15782170 DOI: 10.1038/Nmeth1104-104 |
0.35 |
|
| 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 |
0.351 |
|
| 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 |
0.648 |
|
| 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 |
0.35 |
|
| 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 |
0.332 |
|
| 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 |
0.365 |
|
| 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 |
0.323 |
|
| 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 |
0.32 |
|
| 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 |
0.664 |
|
| 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 |
0.637 |
|
| 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 |
0.35 |
|
| 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 |
0.314 |
|
| 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 |
0.358 |
|
| 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 |
0.326 |
|
| 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 |
0.38 |
|
| 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 |
0.396 |
|
| 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 |
0.328 |
|
| 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 |
0.364 |
|
| 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 |
0.301 |
|
| 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 |
0.366 |
|
| 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 |
0.375 |
|
| 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 |
0.337 |
|
| 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 |
0.325 |
|
| 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 |
0.326 |
|
| 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 |
0.342 |
|
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