1: Roche MI, Griesemer I, Khan CM, Moore E, Lin FC, O’Daniel JM, Foreman AKM, Lee
K, Powell BC, Berg JS, Evans JP, Henderson GE, Rini C. Factors influencing
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2: Moore EG, Roche M, Rini C, Corty EW, Girnary Z, O’Daniel JM, Lin FC,
Corbie-Smith G, Evans JP, Henderson GE, Berg JS. Examining the Cascade of
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3: Butterfield RM, Evans JP, Rini C, Kuczynski KJ, Waltz M, Cadigan RJ, Goddard
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4: Meagher KM, Juengst ET, Henderson GE. Grudging Trust and the Limits of
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5: Skinner D, Roche MI, Weck KE, Raspberry KA, Foreman AKM, Strande NT, Berg JS,
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6: Rini C, Khan CM, Moore E, Roche MI, Evans JP, Berg JS, Powell BC, Corbie-Smith
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7: Waltz M, Cadigan RJ, Prince AER, Skinner D, Henderson GE. Age and perceived
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8: Cadigan RJ, Butterfield R, Rini C, Waltz M, Kuczynski KJ, Muessig K, Goddard
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9: Wolf SM, Amendola LM, Berg JS, Chung WK, Clayton EW, Green RC, Harris-Wai J,
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10: Prince AE, Cadigan RJ, Henderson GE, Evans JP, Adams M, Coker-Schwimmer E,
Penn DC, Van Riper M, Corbie-Smith G, Jonas DE. Is there evidence that we should
screen the general population for Lynch syndrome with genetic testing? A
systematic review. Pharmgenomics Pers Med. 2017 Feb 20;10:49-60. doi:
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11: Cadigan RJ, Edwards TP, Lassiter D, Davis AM, Henderson GE.
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12: Cohn EG, Henderson GE, Appelbaum PS. Distributive justice, diversity, and
inclusion in precision medicine: what will success look like? Genet Med. 2017
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13: Tan N, Amendola LM, O’Daniel JM, Burt A, Horike-Pyne MJ, Boshe L, Henderson
GE, Rini C, Roche MI, Hisama FM, Burke W, Wilfond B, Jarvik GP. Is “incidental
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14: Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS,
Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W,
Caga-Anan CF, Chinnaiyan AM, Chung WK, Clayton EW, Cooper GM, East K, Evans JP,
Fullerton SM, Garraway LA, Garrett JR, Gray SW, Henderson GE, Hindorff LA, Holm
IA, Lewis MH, Hutter CM, Janne PA, Joffe S, Kaufman D, Knoppers BM, Koenig BA,
Krantz ID, Manolio TA, McCullough L, McEwen J, McGuire A, Muzny D, Myers RM,
Nickerson DA, Ou J, Parsons DW, Petersen GM, Plon SE, Rehm HL, Roberts JS,
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15: Adams MC, Evans JP, Henderson GE, Berg JS. The promise and peril of genomic
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16: Cadigan RJ, Nelson DK, Henderson GE, Nelson AG, Davis AM. Public Comments on
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17: Henderson GE. With great (participant) rights comes great (researcher)
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18: Khan CM, Rini C, Bernhardt BA, Roberts JS, Christensen KD, Evans JP, Brothers
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19: Khan CM, Rini C, Bernhardt BA, Roberts JS, Christensen KD, Evans JP, Brothers
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20: Cadigan RJ, Lassiter D, Haldeman K, Conlon I, Reavely E, Henderson GE.
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21: Henderson GE, Wolf SM, Kuczynski KJ, Joffe S, Sharp RR, Parsons DW, Knoppers
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22: Edwards T, Cadigan RJ, Evans JP, Henderson GE. Biobanks containing clinical
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23: Henderson GE, Edwards TP, Cadigan RJ, Davis AM, Zimmer C, Conlon I, Weiner
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24: Burke W, Antommaria AH, Bennett R, Botkin J, Clayton EW, Henderson GE, Holm
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25: Henderson GE, Cadigan RJ, Edwards TP, Conlon I, Nelson AG, Evans JP, Davis
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26: Henderson GE, Juengst ET, King NM, Kuczynski K, Michie M. What research
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27: Churchill LR, King NM, Henderson GE. Why we should continue to worry about
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28: Boyer GJ, Whipple W, Cadigan RJ, Henderson GE. Biobanks in the United States:
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29: Beskow LM, Namey EE, Cadigan RJ, Brazg T, Crouch J, Henderson GE, Michie M,
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30: Henderson GE. Is informed consent broken? Am J Med Sci. 2011
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31: Henderson GE, Churchill LR, Davis AM, Easter MM, Grady C, Joffe S, Kass N,
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32: Rivera SM, Brothers KB, Cadigan RJ, Harrell HL, Rothstein MA, Sharp RR,
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33: Lázaro-Muñoz G, Conley JM, Davis AM, Prince AE, Cadigan RJ. Which Results to
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34: Prince AE, Conley JM, Davis AM, Lázaro-Muñoz G, Cadigan RJ. Automatic
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35: Conley JM, Lázaro-Muñoz G, Prince AE, Davis AM, Cadigan RJ. Scientific Social
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36: Long MD, Cadigan RJ, Cook SF, Haldeman K, Kuczynski K, Sandler RS, Martin CF,
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37: Isler MR, Sutton K, Cadigan RJ, Corbie-Smith G. Community perceptions of
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38: Conley JM, Mitchell R, Cadigan RJ, Davis AM, Dobson AW, Gladden RQ. A trade
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39: Michie M, Cadigan RJ, Henderson G, Beskow LM. Am I a control?:
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40: Cadigan RJ, Michie M, Henderson G, Davis AM, Beskow LM. The meaning of
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41: Mitchell R, Conley JM, Davis AM, Cadigan RJ, Dobson AW, Gladden RQ. Genomics.
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42: Juengst ET, McGowan ML. Why Does the Shift from “Personalized Medicine” to
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43: Johnston J, Juengst E. Are Parents Really Obligated to Learn as Much as
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44: Kaye J, Terry SF, Juengst E, Coy S, Harris JR, Chalmers D, Dove ES,
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45: Juengst ET. Crowdsourcing the Moral Limits of Human Gene Editing? Hastings
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46: Meagher KM, McGowan ML, Settersten RA Jr, Fishman JR, Juengst ET. Precisely
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47: Juengst E, McGowan ML, Fishman JR, Settersten RA Jr. From “Personalized” to
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48: Woolley JP, McGowan ML, Teare HJ, Coathup V, Fishman JR, Settersten RA Jr,
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49: Lázaro-Muñoz G, Conley JM, Davis AM, Van Riper M, Walker RL, Juengst ET.
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50: Lázaro-Muñoz G, Juengst ET. CHALLENGES FOR IMPLEMENTING A PTSD PREVENTIVE
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51: Berg JS, Foreman AK, O’Daniel JM, Booker JK, Boshe L, Carey T, Crooks KR,
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52: Lázaro-Muñoz G, Conley JM, Davis AM, Van Riper M, Walker RL, Juengst ET.
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53: McGowan ML, Fishman JR, Settersten RA Jr, Lambrix MA, Juengst ET. Gatekeepers
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54: Juengst ET, Fishman JR, McGowan ML, Settersten RA Jr. Serving epigenetics
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55: Walker RL, Juengst ET, Whipple W, Davis AM. Genomic research with the newly
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56: Burke W, Appelbaum P, Dame L, Marshall P, Press N, Pyeritz R, Sharp R,
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57: Choudhury S, Fishman JR, McGowan ML, Juengst ET. Big data, open science and
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58: Juengst ET. TMI! ethical challenges in managing and using large patient data
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59: McGowan ML, Settersten RA Jr, Juengst ET, Fishman JR. Integrating genomics
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60: Holm IA, Savage SK, Green RC, Juengst E, McGuire A, Kornetsky S, Brewster SJ,
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63: Kaye J, Meslin EM, Knoppers BM, Juengst ET, Deschênes M, Cambon-Thomsen A,
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64: Dressler LG, Smolek S, Ponsaran R, Markey JM, Starks H, Gerson N, Lewis S,
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65: Mehlman MJ, Berg JW, Juengst ET, Kodish E. Ethical and legal issues in
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66: Coors ME, Glover JJ, Juengst ET, Sikela JM. The ethics of using transgenic
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67: Callier SL, Huss J, Juengst ET. GINA and preemployment criminal background
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76: Tomlinson AN, Skinner D, Perry DL, Scollon SR, Roche MI, Bernhardt BA. “Not
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77: Haase R, Michie M, Skinner D. Flexible positions, managed hopes: the
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79: Skinner D, Choudhury S, Sideris J, Guarda S, Buansi A, Roche M, Powell C,
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80: Raspberry KA, Skinner D. Negotiating desires and options: how mothers who
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81: Raspberry K, Skinner D. Enacting genetic responsibility: experiences of
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82: Bailey DB Jr, Skinner D, Roche MI, Powell C. Emerging dilemmas in newborn
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83: Roche MI, Skinner D. How parents search, interpret, and evaluate genetic
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84: Bailey DB Jr, Armstrong FD, Kemper AR, Skinner D, Warren SF. Supporting
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85: Schaffer R, Kuczynski K, Skinner D. Producing genetic knowledge and
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86: Raspberry K, Skinner D. Experiencing the genetic body: parents’ encounters
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87: Bailey DB Jr, Beskow LM, Davis AM, Skinner D. Changing perspectives on the
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88: Conley JM, Cook-Deegan R, Lázaro-Muñoz G. MYRIAD AFTER MYRIAD: THE
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89: Cook-Deegan R, Conley JM, Evans JP, Vorhaus D. The next controversy in
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90: Conley JM, Doerr AK, Vorhaus DB. Enabling responsible public genomics. Health
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91: Webber EM, Hunter JE, Biesecker LG, Buchanan AH, Clarke EV, Currey E,
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92: Haskell GT, Adams MC, Fan Z, Amin K, Guzman Badillo RJ, Zhou L, Bizon C,
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93: Bush LW, Beck AE, Biesecker LG, Evans JP, Hamosh A, Holm IA, Martin CL,
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94: Evans JP, Powell BC, Berg JS. Finding the Rare Pathogenic Variants in a Human
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95: Allyse M, Evans JP, Michie M. Dr. Pangloss’s Clinic: Prenatal Whole Genome
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96: May T, Strong KA, Zusevics KL, Jeruzal J, Farrell MH, LaPean Kirschner A,
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97: May T, Evans JP, Strong KA, Zusevics KL, Derse AR, Jeruzal J, LaPean
Kirschner A, Farrell MH, Grotevant HD. Issues of “Cost, Capabilities, and Scope”
in Characterizing Adoptees’ Lack of “Genetic-Relative Family Health History” as
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Health Disparity for Adoptees?” Am J Bioeth. 2016 Dec;16(12):W4-W8. PubMed PMID:
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98: Kalia SS, Adelman K, Bale SJ, Chung WK, Eng C, Evans JP, Herman GE, Hufnagel
SB, Klein TE, Korf BR, McKelvey KD, Ormond KE, Richards CS, Vlangos CN, Watson M,
Martin CL, Miller DT. Recommendations for reporting of secondary findings in
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99: O’Daniel JM, McLaughlin HM, Amendola LM, Bale SJ, Berg JS, Bick D, Bowling
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M, Hindorff LA, Holm IA, Jarvik GP, Knight Johnson A, Mighion L, Morra M, Plon
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SM, Yang Y, Rehm HL. A survey of current practices for genomic sequencing test
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100: Evans JP. (Mis)understanding Science: The Problem with Scientific
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101: Hunter JE, Irving SA, Biesecker LG, Buchanan A, Jensen B, Lee K, Martin CL,
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AF, Slavotinek A, Sobreira N, Strande N, Weaver M, Webber EM, Williams MS, Berg
JS, Evans JP, Goddard KA. A standardized, evidence-based protocol to assess
clinical actionability of genetic disorders associated with genomic variation.
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102: Khoury MJ, Evans JP. A public health perspective on a national precision
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103: Rehm HL, Berg JS, Brooks LD, Bustamante CD, Evans JP, Landrum MJ, Ledbetter
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104: Janssens AC, Evans JP. Returning pharmacogenetic secondary findings from
genome sequencing: let’s not put the cart before the horse. Genet Med. 2015
Nov;17(11):854-6. doi: 10.1038/gim.2015.59. Epub 2015 May 7. PubMed PMID:
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105: Lee K, Berg JS, Milko L, Crooks K, Lu M, Bizon C, Owen P, Wilhelmsen KC,
Weck KE, Evans JP, Garg S. High Diagnostic Yield of Whole Exome Sequencing in
Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting. Am J
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106: May T, Strong KA, Khoury MJ, Evans JP. Can targeted genetic testing offer
useful health information to adoptees? Genet Med. 2015 Jul;17(7):533-5. doi:
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107: Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH,
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Burt A, Jamal SM, Abrudan JL, Johnson AD, Conlin LK, Dulik MC, Santani A,
Metterville DR, Kelly M, Foreman AK, Lee K, Taylor KD, Guo X, Crooks K,
Kiedrowski LA, Raffel LJ, Gordon O, Machini K, Desnick RJ, Biesecker LG, Lubitz
SA, Mulchandani S, Cooper GM, Joffe S, Richards CS, Yang Y, Rotter JI, Rich SS,
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Bird T, Sybert VP, Grady WM, Tabor HK, Kim JH, Bamshad MJ, Wilfond B, Motulsky
AG, Scott CR, Pritchard CC, Walsh TD, Burke W, Raskind WH, Byers P, Hisama FM,
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108: Evans JP, Watson MS. Genetic testing and FDA regulation: overregulation
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109: Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, Evans BJ,
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Lehmann LS, McCarty C, Prows CA, Rehm HL, Sharp RR, Salama J, Sanderson S, Van
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110: Foreman AK, Lee K, Evans JP. The NCGENES project: exploring the new world of
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111: Adams SD, Evans JP, Aylsworth AS. Direct-to-consumer genomic testing offers
little clinical utility but appears to cause minimal harm. N C Med J. 2013
Nov-Dec;74(6):494-8. PubMed PMID: 24316774.

112: Berg JS, Amendola LM, Eng C, Van Allen E, Gray SW, Wagle N, Rehm HL, DeChene
ET, Dulik MC, Hisama FM, Burke W, Spinner NB, Garraway L, Green RC, Plon S, Evans
JP, Jarvik GP; Members of the CSER Actionability and Return of Results Working
Group. Processes and preliminary outputs for identification of actionable genes
as incidental findings in genomic sequence data in the Clinical Sequencing
Exploratory Research Consortium. Genet Med. 2013 Nov;15(11):860-7. doi:
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113: Evans JP. Finding common ground. Genet Med. 2013 Nov;15(11):852-3. doi:
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114: Evans JP. Return of results to the families of children in genomic
sequencing: tallying risks and benefits. Genet Med. 2013 Jun;15(6):435-6. doi:
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115: Evans JP. When is a medical finding “incidental”? Genet Med. 2013
Jul;15(7):515-6. doi: 10.1038/gim.2013.74. Epub 2013 May 30. PubMed PMID:
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116: McGuire AL, McCullough LB, Evans JP. The indispensable role of professional
judgment in genomic medicine. JAMA. 2013 Apr 10;309(14):1465-6. doi:
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117: Evans JP, Berg JS, Olshan AF, Magnuson T, Rimer BK. We screen newborns,
don’t we?: realizing the promise of public health genomics. Genet Med. 2013
May;15(5):332-4. doi: 10.1038/gim.2013.11. Epub 2013 Mar 7. Review. PubMed PMID:
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118: Evans JP, Khoury MJ. The arrival of genomic medicine to the clinic is only
the beginning of the journey. Genet Med. 2013 Apr;15(4):268-9. doi:
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119: Dobson AW, Evans JP. Gene patents in the US–focusing on what really
matters. Genome Biol. 2012 Jun 29;13(6):161. doi: 10.1186/gb-2012-13-6-161.
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120: Evans JP, Rothschild BB. Return of results: not that complicated? Genet Med.
2012 Apr;14(4):358-60. doi: 10.1038/gim.2012.8. PubMed PMID: 22481183.

121: Green RC, Berg JS, Berry GT, Biesecker LG, Dimmock DP, Evans JP, Grody WW,
Hegde MR, Kalia S, Korf BR, Krantz I, McGuire AL, Miller DT, Murray MF, Nussbaum
RL, Plon SE, Rehm HL, Jacob HJ. Exploring concordance and discordance for return
of incidental findings from clinical sequencing. Genet Med. 2012
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122: Evans JP, Berg JS. Next-generation DNA sequencing, regulation, and the
limits of paternalism: the next challenge. JAMA. 2011 Dec 7;306(21):2376-7. doi:
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123: Spencer DH, Lockwood C, Topol E, Evans JP, Green RC, Mansfield E, Tezak Z.
Direct-to-consumer genetic testing: reliable or risky? Clin Chem. 2011
Dec;57(12):1641-4. doi: 10.1373/clinchem.2011.167197. Epub 2011 Sep 1. PubMed
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124: Dreyfuss R, Evans JP. From Bilski back to Benson: preemption, inventing
around, and the case of genetic diagnostics. Stanford Law Rev. 2011
Jun;63(6):1349-76. PubMed PMID: 21774194.

125: Burke W, Tarini B, Press NA, Evans JP. Genetic screening. Epidemiol Rev.
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126: Evans JP. That personal touch. Hastings Cent Rep. 2011 May-Jun;41(3):5-6.
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127: Berg JS, Khoury MJ, Evans JP. Deploying whole genome sequencing in clinical
practice and public health: meeting the challenge one bin at a time. Genet Med.
2011 Jun;13(6):499-504. doi: 10.1097/GIM.0b013e318220aaba. PubMed PMID: 21558861.

128: Khoury MJ, Bowen MS, Burke W, Coates RJ, Dowling NF, Evans JP, Reyes M, St
Pierre J. Current priorities for public health practice in addressing the role of
human genomics in improving population health. Am J Prev Med. 2011
Apr;40(4):486-93. doi: 10.1016/j.amepre.2010.12.009. PubMed PMID: 21406285;
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129: Evans JP. Looking ahead, looking behind. Introduction. Genet Med. 2011
Mar;13(3):177-8. doi: 10.1097/GIM.0b013e318210b0a7. PubMed PMID: 21346480.

130: Evans JP, Meslin EM, Marteau TM, Caulfield T. Genomics. Deflating the
genomic bubble. Science. 2011 Feb 18;331(6019):861-2. doi:
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131: Khoury MJ, Coates RJ, Evans JP. Evidence-based classification of
recommendations on use of genomic tests in clinical practice: dealing with
insufficient evidence. Genet Med. 2010 Nov;12(11):680-3. doi:
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132: Evans JP, Dale DC, Fomous C. Preparing for a consumer-driven genomic age. N
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133: Evans JP. The Human Genome Project at 10 years: a teachable moment. Genet
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134: Evans JP, Burke W, Khoury M. The rules remain the same for genomic medicine:
the case against “reverse genetic exceptionalism”. Genet Med. 2010
Jun;12(6):342-3. doi: 10.1097/GIM.0b013e3181deb308. PubMed PMID: 20556868.

135: Evans JP. Putting patients before patents. Genet Med. 2010 Apr;12(4):204-5.
doi: 10.1097/GIM.0b013e3181d74c1c. PubMed PMID: 20395743.

136: Evans JP. The Origin. Genet Med. 2009 Nov;11(11):776-7. doi:
10.1097/GIM.0b013e3181c03a17. PubMed PMID: 19938246.

137: Ader T, Susswein LR, Callanan NP, Evans JP. Attitudes and practice of
genetic counselors regarding anonymous testing for BRCA1/2. J Genet Couns. 2009
Dec;18(6):606-17. doi: 10.1007/s10897-009-9250-z. Epub 2009 Oct 2. PubMed PMID:
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138: Grosse SD, McBride CM, Evans JP, Khoury MJ. Personal utility and genomic
information: look before you leap. Genet Med. 2009 Aug;11(8):575-6. doi:
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139: Evans JP, Green RC. Direct to consumer genetic testing: Avoiding a culture
war. Genet Med. 2009 Aug;11(8):568-9. doi: 10.1097/GIM.0b013e3181afbaed. PubMed
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140: Evans JP. The voyage continues: Darwin and medicine at 200 years. JAMA. 2009
Feb 11;301(6):663-5. doi: 10.1001/jama.2009.102. PubMed PMID: 19211473.

141: Evans JP. Recreational genomics; what’s in it for you? Genet Med. 2008
Oct;10(10):709-10. doi: 10.1097/GIM.0b013e3181859959. PubMed PMID: 18813136;
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142: Evans JP, Burke W. Genetic exceptionalism. Too much of a good thing? Genet
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143: Robin NH, Evans JP. Why physicians must understand evolution. Curr Opin
Pediatr. 2009 Dec;21(6):699-702. doi: 10.1097/MOP.0b013e3283323aa8. Review.
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144: Evans JP. Health care in the age of genetic medicine. Genet Med. 2008
Jan;10(1):1-3. doi: 10.1097/GIM.0b013e318164c669. Review. PubMed PMID: 18197050.

145: Susswein LR, Skrzynia C, Lange LA, Booker JK, Graham ML 3rd, Evans JP.
Increased uptake of BRCA1/2 genetic testing among African American women with a
recent diagnosis of breast cancer. J Clin Oncol. 2008 Jan 1;26(1):32-6. doi:
10.1200/JCO.2007.10.6377. PubMed PMID: 18165638.

146: Evans JP. Health care in the age of genetic medicine. JAMA. 2007 Dec
12;298(22):2670-2. PubMed PMID: 18073364.

147: Evans JP. A future for medical genetics: lessons from Catch 22. Genet Med.
2007 Jan;9(1):1-3. PubMed PMID: 17224683.

148: Evans JP. Celebrating the birthday of our intellectual common ancestor.
Genet Med. 2007 Feb;9(2):63-4. PubMed PMID: 17304045.

149: Milko LV, Rini C, Lewis MA, Butterfield RM, Lin FC, Paquin RS, Powell BC,
Roche MI, Souris KJ, Bailey DB Jr, Berg JS, Powell CM. Evaluating parents’
decisions about next-generation sequencing for their child in the NC NEXUS (North
Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized
controlled trial protocol. Trials. 2018 Jun 28;19(1):344. doi:
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150: Ormond KE, Hallquist MLG, Buchanan AH, Dondanville D, Cho MK, Smith M, Roche
M, Brothers KB, Coughlin CR 2nd, Hercher L, Hudgins L, Jamal S, Levy HP, Raskin
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151: Amendola LM, Robinson JO, Hart R, Biswas S, Lee K, Bernhardt BA, East K,
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152: Lewis MA, Stine A, Paquin RS, Mansfield C, Wood D, Rini C, Roche MI, Powell
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