Publications related to the CEPH Families Reference Panel

Sasani TA, Pedersen BS, Gao Z, Baird L, Przeworski M, Jorde LB, Quinlan AR. Large, three-generation human families reveal post-zygotic mosaicism and variability in germline mutation accumulation. Elife. 2019 Sep 24;8. pii: e46922. doi: 10.7554/eLife.46922.

Thibord F, Hardy L, Ibrahim-Kosta M, Saut N, Pulcrano-Nicolas AS, Goumidi L, Civelek M, Eriksson P, Deleuze JF, Le Goff W, Trégouët DA, Morange PE. A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process. J Thromb Haemost. 2019 Jul 4. doi: 10.1111/jth.14562. [Epub ahead of print]

Yu EY, Wesselius A, van Osch F, Stern MC, Jiang X, Kellen E, Lu CM, Pohlabeln H, Steineck G, Marshall J, Allam MF, La Vecchia C, Johnson KC, Benhamou S, Zhang ZF, Bosetti C, Taylor JA, Zeegers MP. The association between coffee consumption and bladder cancer in the bladder cancer epidemiology and nutritional determinants (BLEND) international pooled study. Cancer Causes Control. 2019 Aug;30(8):859-870. doi: 10.1007/s10552-019-01191-1. Epub 2019 May 30

Moorjani P, Sankararaman S, Fu Q, Przeworski M, Patterson N, Reich D A genetic method for dating ancient genomes provides a direct estimate of human generation interval in the last 45,000 years. Proc Natl Acad Sci U S A. 2016 May 17;113(20):5652-7. doi: 10.1073/pnas.1514696113.

Xiang Y, Guo J, Peng YF, Lan Y, Huang HT, Wei YS [Distribution of single nucleotide polymorphisms of arginine-vasopressin gene in Guangxi healthy population]. Nan Fang Yi Ke Da Xue Xue Bao. 2016 Jun 20;36(7):927-31. Chinese. .

Polley S, Cipriani V, Khan JC, Shahid H, Moore AT, Yates JR, Hollox EJ Analysis of copy number variation at DMBT1 and age-related macular degeneration. BMC Med Genet. 2016 Jul 15;17(1):44. doi: 10.1186/s12881-016-0311-5.

Kim YC, Cui J, Luo J, Xiao F, Downs B, Wang SM Exome-based Variant Detection in Core Promoters. Sci Rep. 2016 Jul 28;6:30716. doi: 10.1038/srep30716.

Al-Sadat N, Majid HA, Sim PY, Su TT, Dahlui M, Abu Bakar MF, Dzaki N, Norbaya S, Murray L, Cantwell MM, Jalaludin MY; MyHeART study group Vitamin D deficiency in Malaysian adolescents aged 13 years: findings from the Malaysian Health and Adolescents Longitudinal Research Team study (MyHeARTs). BMJ Open. 2016 Aug 18;6(8):e010689. doi: 10.1136/bmjopen-2015-010689.

Brenner DR, Brennan P, Boffetta P, Amos CI, Spitz MR, Chen C, Goodman G, Heinrich J, Bickeböller H, Rosenberger A, Risch A, Muley T, McLaughlin JR, Benhamou S, Bouchardy C, Lewinger JP, Witte JS, Chen G, Bull S, Hung RJ Erratum to: Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls. Hum Genet. 2016 Aug;135(8):963. No abstract available. .

Rume FI, Ahsan CR, Biswas PK, Yasmin M, Braun P, Walter MC, Antwerpen M, Grass G, Hanczaruk M Unexpected genomic relationships between Bacillus anthracis strains from Bangladesh and Central Europe. Infect Genet Evol. 2016 Aug 16;45:66-74. doi: 10.1016/j.meegid.2016.08.017.

Iotchkova V, Huang J, Morris JA, Jain D, Barbieri C, Walter K, Min JL, Chen L, Astle W, Cocca M, Deelen P, Elding H, Farmaki AE, Franklin CS, Franberg M, Gaunt TR, Hofman A, Jiang T, Kleber ME, Lachance G, Luan J, Malerba G, Matchan A, Mead D, Memari Y, Ntalla I, Panoutsopoulou K, Pazoki R, Perry JR, Rivadeneira F, Sabater-Lleal M, Sennblad B, Shin SY, Southam L, Traglia M, van Dijk F, van Leeuwen EM, Zaza G, Zhang W,Amin N, Butterworth A, Chambers JC, Dedoussis G, Dehghan A, Franco OH, Franke L, Frontini M, Gambaro G, Gasparini P, Hamsten A, Issacs A, Kooner JS, Kooperberg C, Langenberg C, Marz W, Scott RA, Swertz MA, Toniolo D, Uitterlinden AG, van Duijn CM, Watkins H, Zeggini E, Maurano MT, Timpson NJ, Reiner AP, Auer PL, Soranzo N. Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. Nat Genet. 2016 Sep 26. doi: 10.1038/ng.3668.

Wright GE, Carleton B, Hayden MR, Ross CJ The global spectrum of protein-coding pharmacogenomic diversity. Pharmacogenomics J. 2016 Oct 25. doi: 10.1038/tpj.2016.77.

Kanai M, Tanaka T, Okada Y Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set. J Hum Genet. 2016 Oct;61(10):861-866. doi: 10.1038/jhg.2016.72.

Adams HH, Hibar DP, Chouraki V, Stein JL, Nyquist PA, Renteria ME, Trompet S, Arias-Vasquez A, Seshadri S, Desrivières S, Beecham AH, Jahanshad N, Wittfeld K, Van der Lee SJ, Abramovic L, Alhusaini S, Amin N, Andersson M, Arfanakis K, Aribisala BS, Armstrong NJ, Athanasiu L, Axelsson T, Beiser A, Bernard M, Bis JC, Blanken LM, Blanton SH, Bohlken MM, Boks MP, Bralten J, Brickman AM, Carmichael O, Chakravarty MM, Chauhan G, Chen Q, Ching CR, Cuellar-Partida G, Braber AD, Doan NT, Ehrlich S, Filippi I, Ge T, Giddaluru S, Goldman AL, Gottesman RF, Greven CU, Grimm O, Griswold ME, Guadalupe T, Hass J, Haukvik UK, Hilal S, Hofer E, Hoehn D, Holmes AJ, Hoogman M, Janowitz D, Jia T, Kasperaviciute D, Kim S, Klein M, Kraemer B, Lee PH, Liao J, Liewald DC, Lopez LM, Luciano M, Macare C, Marquand A, Matarin M, Mather KA, Mattheisen M, Mazoyer B, McKay DR, McWhirter R, Milaneschi Y, Mirza-Schreiber N, Muetzel RL, Maniega SM, Nho K, Nugent AC, Loohuis LM, Oosterlaan J, Papmeyer M, Pappa I, Pirpamer L, Pudas S, Pütz B, Rajan KB, Ramasamy A, Richards JS, Risacher SL, Roiz-Santiañez R, Rommelse N, Rose EJ, Royle NA, Rundek T, Sämann PG, Satizabal CL, Schmaal L, Schork AJ, Shen L, Shin J, Shumskaya E, Smith AV, Sprooten E, Strike LT, Teumer A, Thomson R, Tordesillas-Gutierrez D, Toro R, Trabzuni D, Vaidya D, Van der Grond J, Van der Meer D, Van Donkelaar MM, Van Eijk KR, Van Erp TG, Van Rooij D, Walton E, Westlye LT, Whelan CD, Windham BG, Winkler AM, Woldehawariat G, Wolf C, Wolfers T, Xu B, Yanek LR, Yang J, Zijdenbos A, Zwiers MP, Agartz I, Aggarwal NT, Almasy L, Ames D, Amouyel P, Andreassen OA, Arepalli S, Assareh AA, Barral S, Bastin ME, Becker DM, Becker JT, Bennett DA, Blangero J, van Bokhoven H, Boomsma DI, Brodaty H, Brouwer RM, Brunner HG, Buckner RL, Buitelaar JK, Bulayeva KB, Cahn W, Calhoun VD, Cannon DM, Cavalleri GL, Chen C, Cheng CY, Cichon S, Cookson MR, Corvin A, Crespo-Facorro B, Curran JE, Czisch M, Dale AM, Davies GE, De Geus EJ, De Jager PL, de Zubicaray GI, Delanty N, Depondt C, DeStefano AL, Dillman A, Djurovic S, Donohoe G, Drevets WC, Duggirala R, Dyer TD, Erk S, Espeseth T, Evans DA, Fedko IO, Fernández G, Ferrucci L, Fisher SE, Fleischman DA, Ford I, Foroud TM, Fox PT, Francks C, Fukunaga M, Gibbs JR, Glahn DC, Gollub RL, Göring HH, Grabe HJ, Green RC, Gruber O, Gudnason V, Guelfi S, Hansell NK, Hardy J, Hartman CA, Hashimoto R, Hegenscheid K, Heinz A, Le Hellard S, Hernandez DG, Heslenfeld DJ, Ho BC, Hoekstra PJ, Hoffmann W, Hofman A, Holsboer F, Homuth G, Hosten N, Hottenga JJ, Pol HE, Ikeda M, Ikram MK, Jr CR, Jenkinson M, Johnson R, Jönsson EG, Jukema JW, Kahn RS, Kanai R, Kloszewska I, Knopman DS, Kochunov P, Kwok JB, Lawrie SM, Lemaître H, Liu X, Longo DL, Jr WT, Lopez OL, Lovestone S, Martinez O, Martinot JL, Mattay VS, McDonald C, McIntosh AM, McMahon KL, McMahon FJ, Mecocci P, Melle I, Meyer-Lindenberg A, Mohnke S, Montgomery GW, Morris DW, Mosley TH, Mühleisen TW, Müller-Myhsok B, Nalls MA, Nauck M, Nichols TE, Niessen WJ, Nöthen MM, Nyberg L, Ohi K, Olvera RL, Ophoff RA, Pandolfo M, Paus T, Pausova Z, Penninx BW, Pike GB, Potkin SG, Psaty BM, Reppermund S, Rietschel M, Roffman JL, Romanczuk-Seiferth N, Rotter JI, Ryten M, Sacco RL, Sachdev PS, Saykin AJ, Schmidt R, Schofield PR, Sigurdsson S, Simmons A, Singleton A, Sisodiya SM, Smith C, Smoller JW, Soininen H, Srikanth V, Steen VM, Stott DJ, Sussmann JE, Thalamuthu A, Tiemeier H, Toga AW, Traynor BJ, Troncoso J, Turner JA, Tzourio C, Uitterlinden AG, Hernández MC, Van der Brug M, Van der Lugt A, Van der Wee NJ, Van Duijn CM, Van Haren NE, Van T Ent D, Van Tol MJ, Vardarajan BN, Veltman DJ, Vernooij MW, Völzke H, Walter H, Wardlaw JM, Wassink TH, Weale ME, Weinberger DR, Weiner MW, Wen W, Westman E, White T, Wong TY, Wright CB, Zielke HR, Zonderman AB, Deary IJ, DeCarli C, Schmidt H, Martin NG, De Craen AJ, Wright MJ, Launer LJ, Schumann G, Fornage M, Franke B, Debette S, Medland SE, Ikram MA, Thompson PM Novel genetic loci underlying human intracranial volume identified through genome-wide association. Nat Neurosci. 2016 Oct 3. doi: 10.1038/nn.4398.

Loh PR, Danecek P, Palamara PF, Fuchsberger C, A Reshef Y, K Finucane H, Schoenherr S, Forer L, McCarthy S, Abecasis GR, Durbin R, L Price A Reference-based phasing using the Haplotype Reference Consortium panel. Nat Genet. 2016 Oct 3. doi: 10.1038/ng.3679.

Taherzadeh G, Zhou Y, Liew AW, Yang Y Sequence-Based Prediction of Protein-Carbohydrate Binding Sites Using Support Vector Machines. J Chem Inf Model. 2016 Oct 24;56(10):2115-2122.

Tran Q, Gao S, Phan V Analysis of optimal alignments unfolds aligners' bias in existing variant profiles. BMC Bioinformatics. 2016 Oct 6;17(Suppl 13):349.

Liu G, Zhang F, Hu Y, Jiang Y, Gong Z, Liu S, Chen X, Jiang Q, Hao J Genetic Variants and Multiple Sclerosis Risk Gene SLC9A9 Expression in Distinct Human Brain Regions. Mol Neurobiol. 2016 Oct 20.

Jensen L, Børsting C, Dalhoff K, Morling N Evaluation of the iPLEX® ADME PGx Pro Panel and allele frequencies of pharmacogenetic markers in Danes. Clin Biochem. 2016 Nov;49(16-17):1299-1301. doi: 10.1016/j.clinbiochem.2016.07.014.

Barrie ES, Hartmann K, Lee SH, Frater JT, Seweryn M, Wang D, Sadee W The CHRNA5/CHRNA3/CHRNB4 Nicotinic Receptor Regulome: Genomic Architecture, Regulatory Variants, and Clinical Associations. Hum Mutat. 2016 Oct 19. doi: 10.1002/humu.23135.

Racimo F, Marnetto D, Huerta-Sánchez E Signatures of archaic adaptive introgression in present-day human populations. Mol Biol Evol. 2016 Oct 18. pii: msw216.

Nagai MH, Armelin-Correa LM, Malnic B Monogenic and Monoallelic Expression of Odorant Receptors. Mol Pharmacol. 2016 Nov;90(5):633-639.

Gazal S, Sahbatou M, Babron MC, Génin E, Leutenegger AL. High level of inbreeding in final phase of 1000 Genomes Project. Sci Rep. 2015 Dec 2;5:17453.

Jin TB, Xun XJ, Shi XG, Yuan DY, Feng T, Geng TT, Kang LL. Genetic polymorphisms in very important pharmacogenomic (VIP) variants in the Tibetan population. Genet Mol Res. 2015 Oct 16;14(4):12497-504.

Gahan JM, Byrne MM, Hill M, Quinn EM, Murphy RT, Anney RJ, Ryan AW. Detecting Allelic Expression Imbalance at Candidate Genes Using 5' Exonuclease Genotyping Technology. Methods Mol Biol. 2015;1326:93-103.

Macfarlane CM, Badge RM. Genome-wide amplification of proviral sequences reveals new polymorphic HERV-K(HML-2) proviruses in humans and chimpanzees that are absent from genome assemblies. Retrovirology. 2015 Apr 28;12:35.

Ammar R, Paton TA, Torti D, Shlien A, Bader GD. Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes. F1000Res. 2015 Jan 21;4:17.

Wei YL, Wei L, Zhao L, Sun QF, Jiang L, Zhang T, Liu HB, Chen JG, Ye J, Hu L, Li CX. A single-tube 27-plex SNP assay for estimating individual ancestry and admixture from three continents. Int J Legal Med. 2015 Apr 2.

Mozhui K, Smith AK, Tylavsky FA. Ancestry dependent DNA methylation and influence of maternal nutrition. PLoS One. 2015 Mar 5;10(3):

Bilgin Sonay T, Carvalho T, Robinson MD, Greminger MP, Krützen M, Comas D, Highnam G, Mittelman D, Sharp A, Marques-Bonet T, Wagner A. Tandem repeat variation in human and great ape populations and its impact on gene expression divergence. Genome Res. 2015 Nov;25(11):1591-9.

Tian C, Chen Z, Ma X, Yang M, Wang Z, Dong Y, Yang T, Yang W. Comparison of Genetic Variants in Cancer-Related Genes between Chinese Hui and Han Populations. PLoS One. 2015 Dec 18;10(12):e0145170

Fan BJ, Pasquale LR, Kang JH, Levkovitch-Verbin H, Haines JL, Wiggs JL. Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis. Exp Eye Res. 2015 Oct;139:115-22.

Wenz C, Barbas C, López-Gonzálvez Á, Garcia A, Benavente F, Sanz-Nebot V, Blanc T, Freckleton G, Britz-McKibbin P, Shanmuganathan M, de l'Escaille F, Far J, Haselberg R, Huang S, Huhn C, Pattky M, Michels D, Mou S, Yang F, Neusuess C, Tromsdorf N, Baidoo EE, Keasling JD, Park SS. Interlaboratory study to evaluate the robustness of capillary electrophoresis-mass spectrometry for peptide mapping. J Sep Sci. 2015 Jul 6.

Pagani L, Schiffels S, Gurdasani D, Danecek P, Scally A, Chen Y, Xue Y, Haber M, Ekong R, Oljira T, Mekonnen E, Luiselli D, Bradman N, Bekele E, Zalloua P, Durbin R, Kivisild T, Tyler-Smith C. Tracing the route of modern humans out of Africa by using 225 human genome sequences from Ethiopians and Egyptians. Am J Hum Genet. 2015 Jun 4;96(6):986-91.

Emery LS, Magnaye KM, Bigham AW, Akey JM, Bamshad MJ. Estimates of continental ancestry vary widely among individuals with the same mtDNA haplogroup. Am J Hum Genet. 2015 Feb 5;96(2):183-93.

Zheng HF, Rong JJ, Liu M, Han F, Zhang XW, Richards JB, Wang L. Performance of genotype imputation for low frequency and rare variants from the 1000 genomes. PLoS One. 2015 Jan 26;10(1):e0116487.

Zhang Z, Zheng Y, Zhang X, Liu C, Joyce BT, Kibbe WA, Hou L, Zhang W. Linking short tandem repeat polymorphisms with cytosine modifications in human lymphoblastoid cell lines. Hum Genet. 2016 Feb;135(2):223-32.

Basu A, Sarkar-Roy N, Majumder PP. Genomic reconstruction of the history of extant populations of India reveals five distinct ancestral components and a complex structure. Proc Natl Acad Sci U S A. 2016 Jan 25. pii: 201513197.

Zheng X, Weir BS. Eigenanalysis of SNP data with an identity by descent interpretation. Theor Popul Biol. 2016 Feb;107:65-76.

Yuan Y, Tian L, Lu D, Xu S. Analysis of Genome-Wide RNA-Sequencing Data Suggests Age of the CEPH/Utah (CEU) Lymphoblastoid Cell Lines Systematically Biases Gene Expression Profiles. Sci Rep. 2015 Jan 22;5:7960.

Pikkuhookana P, Sillanpäauml; MJ. Combined linkage disequilibrium and linkage mapping: Bayesian multilocus approach. Heredity (Edinb). 2014 Mar;112(3):351-60.

QuigleyDA, Fiorito E, Nord S, Van Loo P, Alnæs GG, Fleischer T, Tost J, Moen Vollan HK, Tramm T, Overgaard J, Bukholm IR, Hurtado A, Balmain A, Børresen-Dale AL, Kristensen V. The 5p12 breast cancer susceptibility locus affects MRPS30 expression in estrogen-receptor positive tumors. Mol Oncol. 2014 Mar;8(2):273-84.

OkadaY, Diogo D, Greenberg JD, Mouassess F, Achkar WA, Fulton RS, Denny JC, Gupta N, Mirel D, Gabriel S, Li G, Kremer JM, Pappas DA, Carroll RJ, Eyler AE, Trynka G, Stahl EA, Cui J, Saxena R, Coenen MJ, Guchelaar HJ, Huizinga TW, Dieudé P, Mariette X, Barton A, Canhão H, Fonseca JE, de Vries N, Tak PP, Moreland LW, Bridges SL Jr, Miceli-Richard C, Choi HK, Kamatani Y, Galan P, Lathrop M, Raj T, De Jager PL, Raychaudhuri S, Worthington J, Padyukov L, Klareskog L, Siminovitch KA, Gregersen PK, Mardis ER, Arayssi T, Kazkaz LA, Plenge RM. Integration of sequence data from a Consanguineous family with genetic data from an outbred population identifies PLB1 as a candidate rheumatoid arthritis risk gene. PLoS One. 2014 Feb 10;9(2):e87645.

ShiJ, Yang XR, Ballew B, Rotunno M, Calista D, Fargnoli MC, Ghiorzo P, Bressac-de Paillerets B, Nagore E, Avril MF, Caporaso NE, McMaster ML, Cullen M, Wang Z, Zhang X; NCI DCEG Cancer Sequencing Working Group; NCI DCEG Cancer Genomics Research Laboratory; French Familial Melanoma Study Group, Bruno W, Pastorino L, Queirolo P, Banuls-Roca J, Garcia-Casado Z, Vaysse A, Mohamdi H, Riazalhosseini Y, Foglio M, Jouenne F, Hua X, Hyland PL, Yin J, Vallabhaneni H, Chai W, Minghetti P, Pellegrini C, Ravichandran S, Eggermont A, Lathrop M, Peris K, Scarra GB, Landi G, Savage SA, Sampson JN, He J, Yeager M, Goldin LR, Demenais F, Chanock SJ, Tucker MA, Goldstein AM, Liu Y, Landi MT. Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma. Nat Genet. 2014 May;46(5):482-6.

ClearyJG, Braithwaite R, Gaastra K, Hilbush BS, Inglis S, Irvine SA, Jackson A, Littin R, Nohzadeh-Malakshah S, Rathod M, Ware D, Trigg L, De La Vega FM. Joint variant and de novo mutation identification on pedigrees from high-throughput sequencing data. J Comput Biol. 2014 Jun;21(6):405-19.

WangY, McKay JD, Rafnar T, Wang Z, Timofeeva MN, Broderick P, Zong X, Laplana M, Wei Y, Han Y, Lloyd A, Delahaye-Sourdeix M, Chubb D, Gaborieau V, Wheeler W, Chatterjee N, Thorleifsson G, Sulem P, Liu G, Kaaks R, Henrion M, Kinnersley B, Vallée M, LeCalvez-Kelm F, Stevens VL, Gapstur SM, Chen WV, Zaridze D, Szeszenia-Dabrowska N, Lissowska J, Rudnai P, Fabianova E, Mates D, Bencko V, Foretova L, Janout V, Krokan HE, Gabrielsen ME, Skorpen F, Vatten L, Njølstad I, Chen C, Goodman G, Benhamou S, Vooder T, Vãlk K, Nelis M, Metspalu A, Lener M, LubiskiJ, Johansson M, Vineis P, Agudo A, Clavel-Chapelon F, Bueno-de-Mesquita HB, Trichopoulos D, Khaw KT, Johansson M, Weiderpass E, Tjønneland A, Riboli E, Lathrop M, Scelo G, Albanes D, Caporaso NE, Ye Y, Gu J, Wu X, Spitz MR, Dienemann H, Rosenberger A, Su L, Matakidou A, Eisen T, Stefansson K, Risch A, Chanock SJ, Christiani DC, Hung RJ, Brennan P, Landi MT, Houlston RS, Amos CI. Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Nat Genet.

HarianiGD, Lam EJ, Havener T, Kwok PY, McLeod HL, Wagner MJ, Motsinger-Reif AA. Application of next generation sequencing to CEPH cell lines to discover variants associated with FDA approved chemotherapeutics. BMC Res Notes. 2014 Jun 12;7:360.

WangZ, Zhu B, Zhang M, Parikh H, Jia J, Chung CC, Sampson JN, Hoskins JW, Hutchinson A, Burdette L, Ibrahim A, Hautman C, Raj PS, Abnet CC, Adjei AA, Ahlbom A, Albanes D, Allen NE, Ambrosone CB, Aldrich M, Amiano P, Amos C, Andersson U, Andriole G Jr, Andrulis IL, Arici C, Arslan AA, Austin MA, Baris D, Barkauskas DA, Bassig BA, Beane Freeman LE, Berg CD, Berndt SI, Bertazzi PA, Biritwum RB, Black A, Blot W, Boeing H, Boffetta P, Bolton K, Boutron-Ruault MC, Bracci PM, Brennan P, Brinton LA, Brotzman M, Bueno-de-Mesquita HB, Buring JE, Butler MA, Cai Q, Cancel-Tassin G, Canzian F, Cao G, Caporaso NE, Carrato A, Carreon T, Carta A, Chang GC, Chang IS, Chang-Claude J, Che X, Chen CJ, Chen CY, Chen CH, Chen C, Chen KY, Chen YM, Chokkalingam AP, Chu LW, Clavel-Chapelon F, Colditz GA, Colt JS, Conti D, Cook MB, Cortessis VK, Crawford ED, Cussenot O, Davis FG, De Vivo I, Deng X, Ding T, Dinney CP, Di Stefano AL, Diver WR, Duell EJ, Elena JW, Fan JH, Feigelson HS, Feychting M, Figueroa JD, Flanagan AM, Fraumeni JF Jr, Freedman ND, Fridley BL, Fuchs CS, Gago-Dominguez M, Gallinger S, Gao YT, Gapstur SM, Garcia-Closas M, Garcia-Closas R, Gastier-Foster JM, Gaziano JM, Gerhard DS, Giffen CA, Giles GG, Gillanders EM, Giovannucci EL, Goggins M, Gokgoz N, Goldstein AM, Gonzalez C, Gorlick R, Greene MH, Gross M, Grossman HB, Grubb R 3rd, Gu J, Guan P, Haiman CA, Hallmans G, Hankinson SE, Harris CC, Hartge P, Hattinger C, Hayes RB, He Q, Helman L, Henderson BE, Henriksson R, Hoffman-Bolton J, Hohensee C, Holly EA, Hong YC, Hoover RN, Hosgood HD 3rd, Hsiao CF, Hsing AW, Hsiung CA, Hu N, Hu W, Hu Z, Huang MS, Hunter DJ, Inskip PD, Ito H, Jacobs EJ, Jacobs KB, Jenab M, Ji BT, Johansen C, Johansson M, Johnson A, Kaaks R, Kamat AM, Kamineni A, Karagas M, Khanna C, Khaw KT, Kim C, Kim IS, Kim YH, Kim YC, Kim YT, Kang CH, Jung YJ, Kitahara CM, Klein AP, Klein R, Kogevinas M, Koh WP, Kohno T, Kolonel LN, Kooperberg C, Kratz CP, Krogh V, Kunitoh H, Kurtz RC, Kurucu N, Lan Q, Lathrop M, Lau CC, Lecanda F, Lee KM, Lee MP, Le Marchand L, Lerner SP, Li D, Liao LM, Lim WY, Lin D, Lin J, Lindstrom S, Linet MS, Lissowska J, Liu J, Ljungberg B, Lloreta J, Lu D, Ma J, Malats N, Mannisto S, Marina N, Mastrangelo G, Matsuo K, McGlynn KA, McKean-Cowdin R, McNeill LH, McWilliams RR, Melin BS, Meltzer PS, Mensah JE, Miao X, Michaud DS, Mondul AM, Moore LE, Muir K, Niwa S, Olson SH, Orr N, Panico S, Park JY, Patel AV, Patino-Garcia A, Pavanello S, Peeters PH, Peplonska B, Peters U, Petersen GM, Picci P, Pike MC, Porru S, Prescott J, Pu X, Purdue MP, Qiao YL, Rajaraman P, Riboli E, Risch HA, Rodabough RJ, Rothman N, Ruder AM, Ryu JS, Sanson M, Schned A, Schumacher FR, Schwartz AG, Schwartz KL, Schwenn M, Scotlandi K, Seow A, Serra C, Serra M, Sesso HD, Severi G, Shen H, Shen M, Shete S, Shiraishi K, Shu XO, Siddiq A, Sierrasesumaga L, Sierri S, Loon Sihoe AD, Silverman DT, Simon M, Southey MC, Spector L, Spitz M, Stampfer M, Stattin P, Stern MC, Stevens VL, Stolzenberg-Solomon RZ, Stram DO, Strom SS, Su WC, Sund M, Sung SW, Swerdlow A, Tan W, Tanaka H, Tang W, Tang ZZ, Tardon A, Tay E, Taylor PR, Tettey Y, Thomas DM, Tirabosco R, Tjonneland A, Tobias GS, Toro JR, Travis RC, Trichopoulos D, Troisi R, Truelove A, Tsai YH, Tucker MA, Tumino R, Van Den Berg D, Van Den Eeden SK, Vermeulen R, Vineis P, Visvanathan K, Vogel U, Wang C, Wang C, Wang J, Wang SS, Weiderpass E, Weinstein SJ, Wentzensen N, Wheeler W, White E, Wiencke JK, Wolk A, Wolpin BM, Wong MP, Wrensch M, Wu C, Wu T, Wu X, Wu YL, Wunder JS, Xiang YB, Xu J, Yang HP, Yang PC, Yatabe Y, Ye Y, Yeboah ED, Yin Z, Ying C, Yu CJ, Yu K, Yuan JM, Zanetti KA, Zeleniuch-Jacquotte A, Zheng W, Zhou B, Mirabello L, Savage SA, Kraft P, Chanock SJ, Yeager M, Landi MT, Shi J, Chatterjee N, Amundadottir LT. Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15. Hum Mol Genet.

HoggartCJ, Venturini G, Mangino M, Gomez F, Ascari G, Zhao JH, Teumer A, Winkler TW, T. Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index. PLoS Genet.

HaaslRJ, Johnson RC, Payseur BA. The effects of microsatellite selection on linked sequence diversity. Genome Biol Evol. 2014 Jul;6(7):1843-61.

DarlingtonTM, Pimentel R, Smith K, Bakian AV, Jerominski L, Cardon J, Camp NJ, Callor WB, Grey T, Singleton M, Yandell M, Renshaw PF, Yurgelun-Todd DA, Gray D, Coon H. Identifying rare variants for genetic risk through a combined pedigree and phenotype approach: application to suicide and asthma. Transl Psychiatry. 2014 Oct 21;4:e471.

Yuan Y, Tian L, Lu D, Xu S. Analysis of Genome-Wide RNA-Sequencing Data Suggests Age of the CEPH/Utah (CEU) Lymphoblastoid Cell Lines Systematically Biases Gene Expression Profiles. Sci Rep. 2015 Jan 22;5:7960.

Yang S, Liu Y, Jiang N, Chen J, Leach L, Luo Z, Wang M Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals BMC Genomics 2014 Jan 9;15(1):13

Namjou B, Keddache M, Marsolo K, Wagner M, Lingren T, Cobb B, Perry C, Kennebeck S, Holm IA, Li R, Crimmins NA, Martin L, Solti I, Kohane IS, Harley JB EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children Front Genet 2013 Dec 3;4:268

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Banchs I, Bosch A, Guimerà J, Lázaro C, Puig A, Estivill X New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines Hum Mutat 1994;3(4):365-72 Erratum in: Hum Mutat 1994;4(3):232

Jedlicka AE, Taylor EW, Meyers DA, Liu Z, Levitt RC Localization of the highly polymorphic locus D19S120 to 19p13.3 by linkage Cytogenet Cell Genet 1994;65(1-2):140

Wirth B, Pick E, Leutner A, Dadze A, Voosen B, Knapp M, Piechaczek-Wappenschmidt B, Rudnik-Schöneborn S, Schönling J, Cox S, et al Large linkage analysis in 100 families with autosomal recessive spinal muscular atrophy (SMA) and 11 CEPH families using 15 polymorphic loci in the region 5q11.2-q13.3 Genomics 1994 Mar 1;20(1):84-93

Tiller GE, Polumbo PA, Summar ML Linkage mapping of the gene for type III collagen (COL3A1) to human chromosome 2q using a VNTR polymorphism Genomics 1994 Mar 15;20(2):275-7

Menzel S, Stoffel M, Espinosa R 3rd, Fernald AA, Le Beau MM, Bell GI Localization of the glucagon receptor gene to human chromosome band 17q25 Genomics 1994 Mar 15;20(2):327-8

Brett PM, Le Bourdelles B, See CG, Whiting PJ, Attwood J, Woodward K, Robertson MM, Kalsi G, Povey S, Gurling HM Genomic cloning and localization by FISH and linkage analysis of the human gene encoding the primary subunit NMDAR1 (GRIN1) of the NMDA receptor channel Ann Hum Genet 1994 May;58(Pt 2):95-100.

Vora DK, Rosenbloom CL, Beaudet AL, Cottingham RW Polymorphisms and linkage analysis for ICAM-1 and the selectin gene cluster Genomics 1994 Jun;21(3):473-7

Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi G, Lathrop M, Weissenbach J The 1993-94 Généthon human genetic linkage map Nat Genet 1994 Jun;7(2 Spec No):246-339

Glavac D, Ravnik-Glavac M, O'Brien SJ, Dean M Polymorphisms in the 3' untranslated region of the I kappa B/MAD-3 (NFKBI) gene located on chromosome 14 Hum Genet 1994 Jun;93(6):694-6

Schwengel DA, Jedlicka AE, Nanthakumar EJ, Weber JL, Levitt RC Comparison of fluorescence-based semi-automated genotyping of multiple microsatellite loci with autoradiographic techniques Genomics 1994 Jul 1;22(1):46-54

Shen Y, Kozman HM, Thompson A, Phillips HA, Holman K, Nancarrow J, Lane S, Chen LZ, Apostolou S, Doggett NA, et al A PCR-based genetic linkage map of human chromosome 16 Genomics 1994 Jul 1;22(1):68-76

Nemani M, Cherif D, Chesne H, Pelandakis M, Ougen P, Berger R, Weissenbach J, Le Paslier D, Cohen D, Cann HM A YAC contig in 6p23 based on sequence tagged sites Genomics 1994 Jul 15;22(2):388-96

Chyan YJ, Ackerman S, Shepherd NS, McBride OW, Widen SG, Wilson SH, Wood TG The human DNA polymerase beta gene structure Evidence of alternative splicing in gene expression Nucleic Acids Res 1994 Jul 25;22(14):2719-25

Su YR, Klanke CA, Houseal TW, Linn SC, Burk SE, Varvil TS, Otterud BE, Shull GE, Leppert MF, Menon AG Molecular cloning and physical and genetic mapping of the human anion exchanger isoform 3 (SLC2C) gene to chromosome 2q36 Genomics.1994 Aug;22(3):605-9

Biancalana V, Trivier E, Weber C, Weissenbach J, Rowe PS, O'Riordan JL, Partington MW, Heyberger S, Oudet C, Hanauer A Construction of a high-resolution linkage map for Xp22.1-p22.2 and refinement of the genetic localization of the Coffin-Lowry syndrome gene Genomics 1994 Aug;22(3):617-25

Cox DW, Billingsley G, Nguyen VT A linkage map of human chromosome 14, including 13 gene loci Genomics 1994 Sep 15;23(2):331-7

Jones EM, Menzel S, Espinosa R 3rd, Le Beau MM, Bell GI, Takeda J Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism Genomics 1994 Sep 15;23(2):490-1

Carrington M, Stephens JC, Klitz W, Begovich AB, Erlich HA, Mann D Major histocompatibility complex class II haplotypes and linkage disequilibrium values observed in the CEPH families Hum Immunol 1994 Nov;41(3):234-40

Gregg RG, Couch F, Hogan K, Powers PA Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32 Genomics 1993 Jan;15(1):107-12

Avramopoulos D, Cox T, Kraus JP, Chakravarti A, Antonarakis SE Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region Hum Genet 1993 Jan;90(5):566-8

Neuman WL, Westbrook CA, Dixon M, Espinosa R 3rd, Patel YD, Nakamura Y,Weiffenbach B, Le Beau MM Physical localization of 70 polymorphic markers to human chromosome 5 by fluorescence in situ hybridization Cytogenet Cell Genet 1993;62(4):207-10

Schurmans S, Muscatelli F, Miot F, Mattei MG, Vassart G, Parmentier M The OLFR1 gene encoding the HGMP07E putative olfactory receptor maps to the 17p13-->p12 region of the human genome and reveals an MspI restriction fragment length polymorphism Cytogenet Cell Genet 1993;63(3):200-4

March RE, Hollyoake M, Putt W, Hopkinson DA, Edwards YH, Whitehouse DB Genetic polymorphism in the 3' untranslated region of human phosphoglucomutase-1 Ann Hum Genet 1993 Jan;57(Pt 1):1-8

Gregg RG, Powers PA, Hogan K Assignment of the human gene for the beta subunit of the voltage-dependent calcium channel (CACNLB1) to chromosome 17 using somatic cell hybrids and linkage mapping Genomics 1993 Jan;15(1):185-7

Hoehe MR, Ehrenreich H, Otterud B, Caenazzo L, Plaetke R, Zander H, Leppert M The human endothelin-1 gene (EDN1) encoding a peptide with potent vasoactive properties maps distal to HLA on chromosome arm 6p in close linkage to D6S89 Cytogenet Cell Genet 1993;62(2-3):131-5

Royle NJ, Armour JA, Crosier M, Jeffreys AJ Abnormal segregation of alleles in CEPH pedigree DNAs arising from allele loss in lymphoblastoid DNA Genomics 1993 Jan;15(1):119-22

Yi H, Donohue SJ, Klein DC, McBride OW Localization of the hydroxyindole-O-methyltransferase gene to the pseudoautosomal region: implications for mapping of psychiatric disorders Hum Mol Genet 1993 Feb;2(2):127-31

Kumar-Singh R, Wang H, Humphries P, Farrar GJ Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q Am J Hum Genet 1993 Feb;52(2):319-26

Chen H, Kalaitsidaki M, Warren AC, Avramopoulos D, Antonarakis SE A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p Genomics 1993 Mar;15(3):621-5

Koyama K, Emi M, Nakamura Y The cell adhesion regulator (CAR) gene, TaqI and insertion/deletion polymorphisms, and regional assignment to the peritelomeric region of 16q by linkage analysis Genomics 1993 Apr;16(1):264-5

Lázaro C, Gaona A, Ravella A, Volpini V, Casals T, Fuentes JJ, Estivill X Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene Hum Mol Genet 1993 Jun;2(6):725-30

Harvey CB, Fox MF, Jeggo PA, Mantei N, Povey S, Swallow DM Regional localization of the lactase-phlorizin hydrolase gene, LCT, to chromosome 2q21 Ann Hum Genet 1993 Jul;57(Pt 3):179-85

Litt M, Kramer P, Hauge XY, Weber JL, Wang Z, Wilkie PJ, Holt MS, Mishra S, Donis-Keller H, Warnich L, et al A microsatellite-based index map of human chromosome 11 Hum Mol Genet 1993 Jul;2(7):909-13

Johnson B, Brooks BA, Heinzmann C, Diep A, Mohandas T, Sparkes RS, Reyes H, Hoffman E, Lange E, Gatti RA, et al The Ah receptor nuclear translocator gene (ARNT) is located on q21 of human chromosome 1 and on mouse chromosome 3 near Cf-3 Genomics 1993 Sep;17(3):592-8

Richard I, Devaud C, Cherif D, Cohen D, Beckmann JS The gene for creatine kinase, mitochondrial 2 (sarcomeric; CKMT2), maps to chromosome 5q13.3 Genomics 1993 Oct;18(1):134-6

Jabs EW, Li X, Lovett M, Yamaoka LH, Taylor E, Speer MC, Coss C, Cadle R, Hall B, Brown K, et al Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region Genomics 1993 Oct;18(1):7-13

Jorde LB, Watkins WS, Viskochil D, O'Connell P, Ward K Linkage disequilibrium in the neurofibromatosis 1 (NF1) region: implications for gene mapping Am J Hum Genet 1993 Nov;53(5):1038-50

Schwengel DA, Nouri N, Meyers DA, Levitt RC Linkage mapping of the human thromboxane A2 receptor (TBXA2R) to chromosome 19p13.3 using transcribed 3' untranslated DNA sequence polymorphisms Genomics 1993 Nov;18(2):212-5

Gelernter J, Kruger S, Pakstis AJ, Pacholczyk T, Sparkes RS, Kidd KK, Amara S Assignment of the norepinephrine transporter protein (NET1) locus to chromosome 16 Genomics 1993 Dec;18(3):690-2

Nagano K, Nakura J, Kihara K, Ye L, Kamino K, Mitsuda N, Ohta T, Jinno Y, Niikawa N, Miki T, et al Isolation and mapping of microsatellites from a library microdissected from the Werner syndrome region, 8p11.2-p22 Jpn J Hum Genet 1993 Dec;38(4):391-7

Henke A, Fischer C, Rappold GA Genetic map of the human pseudoautosomal region reveals a high rate of recombination in female meiosis at the Xp telomere Genomics 1993 Dec;18(3):478-85

Gelernter J, Pakstis AJ, Grandy D, Litt M, Retief AE, Kennedy JL, Hing-Loh A, Schoolfield G, Civelli O, Kidd KK Linkage map of eight human chromosome 11q markers, including DRD2, spanning 60 cM Cytogenet Cell Genet 1992;60(1):26-8.

Hazan J, Dubay C, Pankowiak MP, Becuwe N, Weissenbach J A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers Genomics 1992 Feb;12(2):183-9

Børglum AD, Byskov A, Ragno P, Roldan AL, Tripputi P, Cassani G, Danø K, Blasi F, Bolund L, Kruse TA Assignment of the urokinase-type plasminogen activator receptor gene (PLAUR) to chromosome 19q13.1-q13.2 Am J Hum Genet 1992 Mar;50(3):492-7

Steinkasserer A, Spurr NK, Cox S, Jeggo P, Sim RB The human IL-1 receptor antagonist gene (IL1RN) maps to chromosome 2q14-q21, in the region of the IL-1 alpha and IL-1 beta loci Genomics 1992 Jul;13(3):654-7

Avramopoulos D, Cox T, Blaschak JE, Chakravarti A, Antonarakis SE Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region Genomics 1992 Oct;14(2):506-7

Eng CM, Durtschi BA, Zoghbi HY, Beaudet AL Isolation, mapping, and characterization of two cDNA clones expressed in the cerebellum Genomics 1992 Nov;14(3):813-5

Oudet C, Hanauer A, Clemens P, Caskey T, Mandel JL Two hot spots of recombination in the DMD gene correlate with the deletion prone regions Hum Mol Genet 1992 Nov;1(8):599-603

Richard I, Broux O, Hillaire D, Cherif D, Fougerousse F, Cohen D, Beckmann JS Mapping of the formin gene and exclusion as a candidate gene for the autosomal recessive form of limb-girdle muscular dystrophy Hum Mol Genet 1992 Nov;1(8):621-4

Nielsen DA, Dean M, Goldman D Genetic mapping of the human tryptophan hydroxylase gene on chromosome 11, using an intronic conformational polymorphism Am J Hum Genet 1992 Dec;51(6):1366-71

Zhong S, Wolf CR, Spurr NK Chromosomal assignment and linkage analysis of the human glutathione S-transferase mu gene (GSTM1) using intron specific polymerase chain reaction Hum Genet 1992 Dec;90(4):435-9

Jabs EW, Warren AC, Taylor EW, Colyer CR, Meyers DA, Antonarakis SE Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both Genomics 1991 Jan;9(1):141-6

Petersen MB, Slaugenhaupt SA, Lewis JG, Warren AC, Chakravarti A, Antonarakis SE A genetic linkage map of 27 markers on human chromosome 21 Genomics 1991 Mar;9(3):407-19

Blanché H, Zoghbi HY, Jabs EW, de Gouyon B, Zunec R, Dausset J, Cann HM A centromere-based genetic map of the short arm of human chromosome 6 Genomics 1991 Mar;9(3):420-8

Alitalo T, Kruse TA, de la Chapelle A Refined localization of the gene causing X-linked juvenile retinoschisis Genomics 1991 Mar;9(3):505-10

Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat Hum Genet 1991 Aug;87(4):401-4

Dean M, Lucas-Derse S, Bolos A, O'Brien SJ, Kirkness EF, Fraser CM, Goldman D Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphism Am J Hum Genet 1991 Sep;49(3):621-6.

Vergnaud G, Mariat D, Apiou F, Aurias A, Lathrop M, Lauthier V The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence Genomics 1991 Sep;11(1):135-44

McInnis MG, Lutfalla G, Slaugenhaupt S, Petersen MB, Uze G, Chakravarti A, Antonarakis SE Linkage mapping of highly informative DNA polymorphisms within the human interferon-alpha receptor gene on chromosome 21 Genomics 1991 Nov;11(3):573-6

Foroud T, Wei S, Ziv Y, Sobel E, Lange E, Chao A, Goradia T, Huo Y, Tolun A, Chessa L, Charmley P, Sanal O, Salman N, Julier C, Concannon P, McConville C, Taylor AM, Shiloh Y, Lange SK, Gatti RA Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: linkage analysis of 111 families by an international consortium Am J Hum Genet 1991 Dec;49(6):1263-79

Huang TH, Hejtmancik JF, Edwards A, Pettigrew AL, Herrera CA, Hammond HA, Caskey CT, Zoghbi HY, Ledbetter DH Linkage of the gene for an X-linked mental retardation disorder to a hypervariable (AGAT)n repeat motif within the human hypoxanthine phosphoribosyltransferase (HPRT) locus (Xq26) Am J Hum Genet 1991 Dec;49(6):1312-9

Coleman MP, Murray JC, Willard HF, Nolan KF, Reid KB, Blake DJ, Lindsay S, Bhattacharya SS, Wright A, Davies KE Genetic and physical mapping around the properdin P gene Genomics 1991 Dec;11(4):991-6

Concannon P, Malhotra U, Charmley P, Reynolds J, Lange K, Gatti RA The ataxia-telangiectasia gene (ATA) on chromosome II is distinct from the ETS-1 gene Am J Hum Genet 1990 Apr;46(4):789-94

Petersen MB, Economou EP, Slaugenhaupt SA, Chakravarti A, Antonarakis SE Linkage analysis of the human HMG14 gene on chromosome 21 using a GT dinucleotide repeat as polymorphic marker Genomics 1990 May;7(1):136-8

Mahtani MM, Willard HF Pulsed-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate Genomics 1990 Aug;7(4):607-13

Lewis JG, Weber JL, Petersen MB, Slaugenhaupt SA, Kwitek A, May PE, Warren AC, Chakravarti A, Antonarakis SE Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat Genomics 1990 Oct;8(2):400-2

Cutting GR, McGinniss MJ, Kasch LM, Tsipouras P, Antonarakis SE Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2 Genomics 1990 Oct;8(2):407-10

Ballabio A, Bardoni B, Guioli S, Basler E, Camerino G Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this region Genomics 1990 Oct;8(2):263-70

Hsieh CL, Bowcock AM, Farrer LA, Hebert JM, Huang KN, Cavalli-Sforza LL, Julius D, Francke U The serotonin receptor subtype 2 locus HTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14 Somat Cell Mol Genet 1990 Nov;16(6):567-74

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Brooks BA, McBride OW, Dolphin CT, Farrall M, Scambler PJ, Gonzalez FJ, Idle JR The gene CYP3 encoding P450pcn1 (nifedipine oxidase) is tightly linked to the gene COL1A2 encoding collagen type 1 alpha on 7q21-q22.1 Am J Hum Genet 1988 Sep;43(3):280-4

Zoghbi HY, O'Brien WE, Ledley FD Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6 Genomics 1988 Nov;3(4):396-8

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