-
1
-
-
84870156368
-
Non-invasive prenatal testing for fetal aneuploidy
-
American College Of Obstetricians And Gynecologists (2012) Committee Opinion No 545
-
American College of Obstetricians and Gynecologists (2012) Committee Opinion No. 545: Non-invasive prenatal testing for fetal aneuploidy. Obstetrics and Gynecology 120(6): 1532-4
-
Obstetrics and Gynecology
, vol.1206
, pp. 1532-1534
-
-
-
2
-
-
84859320067
-
Chromosome-selective sequencing of maternal plasma cell-free dna for first-trimester detection of trisomy 21 and trisomy 18
-
e1-4): 322 e5
-
Ashoor G, Syngelaki A, Wagner M, Birdir C, Nicolaides KH (2012) Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18. American Journal of Obstetrics and Gynecology 206(4): 322 e1-5
-
(2012)
American Journal of Obstetrics and Gynecology
, vol.206
, Issue.4
, pp. 322
-
-
Ashoor, G.1
Syngelaki, A.2
Wagner, M.3
Birdir, C.4
Nicolaides, K.H.5
-
3
-
-
84871532946
-
Trisomy 13 detection in the first trimester of pregnancy using a chromosomeselective cell-free dna analysis method
-
Ashoor G, Syngelaki A, Wang E, Struble C, Oliphant A, Song K, Nicolaides KH (2013) Trisomy 13 detection in the first trimester of pregnancy using a chromosomeselective cell-free DNA analysis method. Ultrasound in Obstetrics and Gynecology 41(1): 21-5
-
(2013)
Ultrasound in Obstetrics and Gynecology
, vol.41
, Issue.1
, pp. 21-25
-
-
Ashoor, G.1
Syngelaki, A.2
Wang, E.3
Struble, C.4
Oliphant, A.5
Song, K.6
Nicolaides, K.H.7
-
4
-
-
84862776853
-
Prenatal detection of down syndrome using massively parallel sequencing (mps): A rapid response statement from a committee on behalf of the board of the international society for prenatal diagnosis, 24 october 2011
-
Benn P, Borrell A, Cuckle H, Dugoff L, Gross S, Johnson JA, Maymon R, Odibo A, Schielen P, Spencer K, Wright D, Yaron Y (2012) Prenatal detection of Down syndrome using massively parallel sequencing (MPS): a rapid response statement from a Committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011. Prenatal Diagnosis 32(1): 1-2
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.1
, pp. 1-2
-
-
Benn, P.1
Borrell, A.2
Cuckle, H.3
Dugoff, L.4
Gross, S.5
Johnson, J.A.6
Maymon, R.7
Odibo, A.8
Schielen, P.9
Spencer, K.10
Wright, D.11
Yaron, Y.12
-
5
-
-
84879487413
-
Non-invasive prenatal testing for aneuploidy: Current status and future prospects
-
Benn P, Cuckle H, Pergament E (2013) Non-invasive prenatal testing for aneuploidy: current status and future prospects. Ultrasound in Obstetrics and Gynecology 42(1): 15-33
-
(2013)
Ultrasound in Obstetrics and Gynecology
, vol.42
, Issue.1
, pp. 15-33
-
-
Benn, P.1
Cuckle, H.2
Pergament, E.3
-
6
-
-
77954139153
-
From michael to microarrays: 30 years of studying fetal cells and nucleic acids in maternal blood
-
Bianchi D (2010) From Michael to microarrays: 30 years of studying fetal cells and nucleic acids in maternal blood. Prenatal Diagnosis 30(7): 622-3
-
(2010)
Prenatal Diagnosis
, vol.30
, Issue.7
, pp. 622-623
-
-
Bianchi, D.1
-
7
-
-
84860213983
-
Maternal blood is source to accurately diagnose fetal aneuploidy (melissa) study group (2012) genome-wide fetal aneuploidy detection by maternal plasma dna sequencing
-
Bianchi DW, Platt LD, Goldberg JD, Abuhamad AZ, Sehnert AJ, Rava RP, MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group (2012) Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing. Obstetrics and Gynecology 119(5): 890-901
-
Obstetrics and Gynecology
, vol.119
, Issue.5
, pp. 890-901
-
-
Bianchi, D.W.1
Platt, L.D.2
Goldberg, J.D.3
Abuhamad, A.Z.4
Sehnert, A.J.5
Rava, R.P.6
-
8
-
-
84861478930
-
Maternal anxiety and pain during prenatal diagnostic techniques: A prospective study
-
Bot-Robin V, Sendon S, Bourzoufi K, Vaast P, Deken V, Dutoit P, Houfflin-Debarge V (2012) Maternal anxiety and pain during prenatal diagnostic techniques: A prospective study. Prenatal Diagnosis 32(6): 562-8
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.6
, pp. 562-568
-
-
Bot-Robin, V.1
Sendon, S.2
Bourzoufi, K.3
Vaast, P.4
Deken, V.5
Dutoit, P.6
Houfflin-Debarge, V.7
-
9
-
-
84864297424
-
Dna sequencing of maternal plasma to identify down syndrome and other trisomies in multiple gestations
-
Canick JA, Kloza EM, Lambert-Messerlian GM, Haddow JE, Ehrich M, van den Boom D, Bombard AT, Deciu C, Palomaki GE (2012) DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations. Prenatal Diagnosis 32(8): 730-4
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.8
, pp. 730-734
-
-
Canick, J.A.1
Kloza, E.M.2
Lambert-Messerlian, G.M.3
Haddow, J.E.4
Ehrich, M.5
Van Den Boom, D.6
Bombard, A.T.7
Deciu, C.8
Palomaki, G.E.9
-
10
-
-
84880035770
-
The impact of maternal plasma dna fetal fraction on next generation sequencing tests for common fetal aneuploidies
-
Canick JA, Palomaki GE, Kloza EM, Lambert-Messerlian GM, Haddow JE (2013) The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies. Prenatal Diagnosis 33(7): 667-74
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.7
, pp. 667-674
-
-
Canick, J.A.1
Palomaki, G.E.2
Kloza, E.M.3
Lambert-Messerlian, G.M.4
Haddow, J.E.5
-
11
-
-
84878125815
-
Uptake of non-invasive prenatal testing (nipt) in women following positive aneuploidy screening
-
Chetty S, Garabedian MJ, Norton ME (2013) Uptake of non-invasive prenatal testing (NIPT) in women following positive aneuploidy screening. Prenatal Diagnosis 33(6): 542-6
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 542-546
-
-
Chetty, S.1
Garabedian, M.J.2
Norton, M.E.3
-
12
-
-
84885727862
-
Antenatal determination of fetal rhesus (rh) d status using cell free fetal dna in the maternal circulation before 20 weeks' gestation: Is routine application practical and beneficial?
-
Fa11-Fa12
-
Chitty LS, Finning G, Massey E, Soothill P, Daniels G (2011a) Antenatal determination of fetal rhesus (RH) D status using cell free fetal DNA in the maternal circulation before 20 weeks' gestation: Is routine application practical and beneficial? Archives of Disease in Childhood Fetal and Neonatal Edition 96(Supplement 1): Fa11-Fa12
-
(2011)
Archives of Disease in Childhood Fetal and Neonatal Edition
, vol.96
, Issue.SUPPL. 1
-
-
Chitty, L.S.1
Finning, G.2
Massey, E.3
Soothill, P.4
Daniels, G.5
-
13
-
-
79951937731
-
New aids for the non-invasive prenatal diagnosis of achondroplasia: Dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal dna in maternal plasma
-
Chitty LS, Griffin DR, Meaney C, Barrett A, Khalil A, Pajkrt E, Cole TJ (2011b) New aids for the non-invasive prenatal diagnosis of achondroplasia: Dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma. Ultrasound in Obstetrics and Gynecology 37(3): 283-9
-
(2011)
Ultrasound in Obstetrics and Gynecology
, vol.37
, Issue.3
, pp. 283-289
-
-
Chitty, L.S.1
Griffin, D.R.2
Meaney, C.3
Barrett, A.4
Khalil, A.5
Pajkrt, E.6
Cole, T.J.7
-
14
-
-
84877625937
-
Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal dna
-
Chitty LS, Khalil A, Barrett AN, Pajkrt E, Griffin DR, Cole TJ (2013) Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA. Prenatal Diagnosis 33(5): 416-23
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.5
, pp. 416-423
-
-
Chitty, L.S.1
Khalil, A.2
Barrett, A.N.3
Pajkrt, E.4
Griffin, D.R.5
Cole, T.J.6
-
15
-
-
84870688045
-
Clinical application of massively parallel sequencing-based prenatal non-invasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors
-
Dan S, Wang W, Ren J, Li Y, Hu H, Xu Z, Lau TK, Xie J, Zhao W, Huang H, Xie J, Sun L, Zhang X, Wang W, Liao S, Qiang R, Cao J, Zhang Q, Zhou Y, Zhu H, Zhong M, Guo Y, Lin L, Gao Z, Yao H, Zhang H, Zhao L, Jiang F, Chen F, Jiang H, Li S, Li Y, Wang J, Wang J, Duan T, Su Y, Zhang X (2012) Clinical application of massively parallel sequencing-based prenatal non-invasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors. Prenatal Diagnosis 32(13): 1225-32
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.13
, pp. 1225-1232
-
-
Dan, S.1
Wang, W.2
Ren, J.3
Li, Y.4
Hu, H.5
Xu, Z.6
Lau, T.K.7
Xie, J.8
Zhao, W.9
Huang, H.10
Xie, J.11
Sun, L.12
Zhang, X.13
Wang, W.14
Liao, S.15
Qiang, R.16
Cao, J.17
Zhang, Q.18
Zhou, Y.19
Zhu, H.20
Zhong, M.21
Guo, Y.22
Lin, L.23
Gao, Z.24
Yao, H.25
Zhang, H.26
Zhao, L.27
Jiang, F.28
Chen, F.29
Jiang, H.30
Li, S.31
Li, Y.32
Wang, J.33
Wang, J.34
Duan, T.35
Su, Y.36
Zhang, X.37
more..
-
16
-
-
59649114083
-
Noninvasive prenatal diagnosis of fetal blood group phenotypes: Current practice and future prospects
-
Daniels G, Finning K, Martin P, Massey E (2009) Noninvasive prenatal diagnosis of fetal blood group phenotypes: Current practice and future prospects. Prenatal Diagnosis 29(2): 101-7
-
(2009)
Prenatal Diagnosis
, vol.29
, Issue.2
, pp. 101-107
-
-
Daniels, G.1
Finning, K.2
Martin, P.3
Massey, E.4
-
17
-
-
84902154595
-
-
Department of Health Report No. 31: Down's syndrome screening.
-
Department of Health (2001) Chief Medical Officer's Update. 2001. Report No. 31: Down's syndrome screening.
-
(2001)
Chief Medical Officer's Update.
, vol.2001
-
-
-
18
-
-
84885519540
-
-
Department of Health, London Department of Health. Department of Health, London
-
Department of Health, London Department of Health (2003) Model of best practice for providing Down's syndrome Screening. Department of Health, London
-
(2003)
Model of Best Practice for Providing Down's Syndrome Screening
-
-
-
19
-
-
79952302397
-
Non-invasive detection of fetal trisomy 21 by sequencing of dna in maternal blood: A study in a clinical setting
-
Ehrich M, Deciu C, Zwiefelhofer T, Tynan JA, Cagasan L, Tim R, Lu V, McCullough R, McCarthy E, Nygren AO, Dean J, Tang L, Hutchison D, Lu T, Wang H, Angkachatchai V, Oeth P, Cantor CR, Bombard A, van den Boom D (2011) Non-invasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: A study in a clinical setting. American Journal of Obstetrics and Gynecology 204(3): 205 e1-e11
-
(2011)
American Journal of Obstetrics and Gynecology
, vol.204
, Issue.3
-
-
Ehrich, M.1
Deciu, C.2
Zwiefelhofer, T.3
Tynan, J.A.4
Cagasan, L.5
Tim, R.6
Lu, V.7
McCullough, R.8
McCarthy, E.9
Nygren, A.O.10
Dean, J.11
Tang, L.12
Hutchison, D.13
Lu, T.14
Wang, H.15
Angkachatchai, V.16
Oeth, P.17
Cantor, C.R.18
Bombard, A.19
Van Den Boom, D.20
more..
-
20
-
-
84878120833
-
Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma dna samples
-
Futch T, Spinosa J, Bhatt S, de Feo E, Rava RP, Sehnert AJ (2013) Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples. Prenatal Diagnosis 33(6): 569-74
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 569-574
-
-
Futch, T.1
Spinosa, J.2
Bhatt, S.3
De Feo, E.4
Rava, R.P.5
Sehnert, A.J.6
-
21
-
-
67649410334
-
How do prospective parents who decline prenatal screening account for their decision? A qualitative study
-
Gottfredsdóttir H, Björnsdóttir K, Sandall J (2009) How do prospective parents who decline prenatal screening account for their decision? A qualitative study. Social Science and Medicine 69(2): 274-7
-
(2009)
Social Science and Medicine
, vol.69
, Issue.2
, pp. 274-277
-
-
Gottfredsdóttir, H.1
Björnsdóttir, K.2
Sandall, J.3
-
22
-
-
79958087361
-
Non-invasive prenatal determination of fetal sex: Translating research into clinical practice
-
Hill M, Finning K, Martin P, Hogg J, Meaney C, Norbury G, Daniels G, Chitty LS (2011) Non-invasive prenatal determination of fetal sex: Translating research into clinical practice. Clinical Genetics 80(1): 68-75
-
(2011)
Clinical Genetics
, vol.80
, Issue.1
, pp. 68-75
-
-
Hill, M.1
Finning, K.2
Martin, P.3
Hogg, J.4
Meaney, C.5
Norbury, G.6
Daniels, G.7
Chitty, L.S.8
-
23
-
-
84869014216
-
Women's and health professionals' preferences for prenatal tests for down syndrome: A discrete choice experiment to contrast noninvasive prenatal diagnosis with current invasive tests
-
Hill M, Fisher J, Chitty LS, Morris S (2012) Women's and health professionals' preferences for prenatal tests for Down syndrome: A discrete choice experiment to contrast noninvasive prenatal diagnosis with current invasive tests. Genetics in Medicine 14(11): 905-13
-
(2012)
Genetics in Medicine
, vol.14
, Issue.11
, pp. 905-913
-
-
Hill, M.1
Fisher, J.2
Chitty, L.S.3
Morris, S.4
-
24
-
-
34548501087
-
Early detection of cell-free fetal DNA in maternal plasma
-
DOI 10.1016/j.earlhumdev.2006.11.001, PII S037837820600301X
-
Illanes S, Denbow M, Kailasam C, Finning K, Soothill PW (2007) Early detection of cell-free fetal DNA in maternal plasma. Early Human Development 83(9): 563-6 (Pubitemid 47380125)
-
(2007)
Early Human Development
, vol.83
, Issue.9
, pp. 563-566
-
-
Illanes, S.1
Denbow, M.2
Kailasam, C.3
Finning, K.4
Soothill, P.W.5
-
25
-
-
84857038661
-
Non-invasive prenatal genetic testing: A study of public attitudes
-
Kelly SE, Farrimond HR (2012) Non-invasive prenatal genetic testing: A study of public attitudes. Public Health Genomics 15(2): 73-81
-
(2012)
Public Health Genomics
, vol.15
, Issue.2
, pp. 73-81
-
-
Kelly, S.E.1
Farrimond, H.R.2
-
26
-
-
84872170213
-
Current controversies in prenatal diagnosis 2: Are we ready to screen for fetal anomalies with first trimester ultrasound?
-
Kontopoulos E, Odibo A, Wilson RD (2013) Current controversies in prenatal diagnosis 2: Are we ready to screen for fetal anomalies with first trimester ultrasound? Prenatal Diagnosis 33(1): 9-12
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.1
, pp. 9-12
-
-
Kontopoulos, E.1
Odibo, A.2
Wilson, R.D.3
-
27
-
-
84878129532
-
Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service
-
Lau TK, Jiang FM, Stevenson RJ, Lo TK, Chan LW, Chan MK, Lo PS, Wang W, Zhang HY, Chen F, Choy KW (2013) Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service. Prenatal Diagnosis 33(6): 602-8
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 602-608
-
-
Lau, T.K.1
Jiang, F.M.2
Stevenson, R.J.3
Lo, T.K.4
Chan, L.W.5
Chan, M.K.6
Lo, P.S.7
Wang, W.8
Zhang, H.Y.9
Chen, F.10
Choy, K.W.11
-
28
-
-
84885600738
-
Non-invasive prenatal testing for down syndrome the views of pregnant women in the uk and their likely uptake
-
Lewis C, Silcock C, Chitty LS (2013) Non-invasive prenatal testing for Down syndrome The views of pregnant women in the UK and their likely uptake. Public Health Genomics 16(5): 223-32
-
(2013)
Public Health Genomics
, vol.16
, Issue.5
, pp. 223-232
-
-
Lewis, C.1
Silcock, C.2
Chitty, L.S.3
-
29
-
-
84899414397
-
Non-invasive prenatal testing for trisomy 21: A crosssectional survey of service users' views and likely uptake
-
DOI: 10.1111/1471-0528.12579
-
Lewis C, Hill M, Silcock C, Daley R, Chitty LS (2014) Non-invasive prenatal testing for trisomy 21: A crosssectional survey of service users' views and likely uptake. BJOG DOI: 10.1111/1471-0528.12579
-
(2014)
BJOG
-
-
Lewis, C.1
Hill, M.2
Silcock, C.3
Daley, R.4
Chitty, L.S.5
-
30
-
-
84877601474
-
Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing
-
Liang D, Lv W, Wang H, Xu L, Liu J, Li H, Hu L, Peng Y, Wu L (2013) Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing. Prenatal Diagnosis 33(5): 409-15
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.5
, pp. 409-415
-
-
Liang, D.1
Lv, W.2
Wang, H.3
Xu, L.4
Liu, J.5
Li, H.6
Hu, L.7
Peng, Y.8
Wu, L.9
-
31
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
DOI 10.1016/S0140-6736(97)02174-0
-
Lo YM, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CW, Wainscoat JS (1997) Presence of fetal DNA in maternal plasma and serum. Lancet 350(9076): 485-7 (Pubitemid 27343304)
-
(1997)
Lancet
, vol.350
, Issue.9076
, pp. 485-487
-
-
Dennis Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
Rai, V.4
Sargent, I.L.5
Redman, C.W.G.6
Wainscoat, J.S.7
-
32
-
-
0033364339
-
Rapid clearance of fetal DNA from maternal plasma
-
DOI 10.1086/302205
-
Lo YM, Zhang J, Leung TN, Lau TK, Chang AM, Hjelm M (1999) Rapid clearance of fetal DNA from maternal plasma. American Journal of Human Genetics 64(1): 218-24 (Pubitemid 30428975)
-
(1999)
American Journal of Human Genetics
, vol.64
, Issue.1
, pp. 218-224
-
-
Dennis Lo, Y.M.1
Zhang, J.2
Leung, T.N.3
Lau, T.K.4
Chang, A.M.Z.5
Magnus Hjelm, N.6
-
33
-
-
78650207098
-
Maternal plasma dna sequencing reveals the genome-wide genetic and mutational profile of the fetus
-
Lo YM, Chan KC, Sun H, Chen EZ, Jiang P, Lun FM, Zheng YW, Leung TY, Lau TK, Cantor CR, Chiu RW (2010) Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus. Science Translational Medicine 2(61): 61-91
-
(2010)
Science Translational Medicine
, vol.2
, Issue.61
, pp. 61-91
-
-
Lo, Y.M.1
Chan, K.C.2
Sun, H.3
Chen, E.Z.4
Jiang, P.5
Lun, F.M.6
Zheng, Y.W.7
Leung, T.Y.8
Lau, T.K.9
Cantor, C.R.10
Chiu, R.W.11
-
34
-
-
0033015696
-
Because of the risks: How US pregnant women account for refusing prenatal screening
-
DOI 10.1016/S0277-9536(99)00097-0, PII S0277953699000970
-
Markens S, Browner CH, Press N (1999) 'Because of the risks': How US pregnant women account for refusing prenatal screening. Social Science and Medicine 49: 359-69 (Pubitemid 29281825)
-
(1999)
Social Science and Medicine
, vol.49
, Issue.3
, pp. 359-369
-
-
Markens, S.1
Browner, C.H.2
Press, N.3
-
36
-
-
51649120342
-
Serum screening with down's syndrome markers to predict pre-eclampsia and small for gestational age: Systematic review and meta-analysis
-
Morris RK, Cnossen JS, Langejans M, Robson SC, Kleijnen J, Ter Riet G, Mol BW, van der Post JA, Khan KS (2008) Serum screening with Down's syndrome markers to predict pre-eclampsia and small for gestational age: Systematic review and meta-analysis. BMC Pregnancy and Childbirth 8: 33
-
(2008)
BMC Pregnancy and Childbirth
, vol.8
, pp. 33
-
-
Morris, R.K.1
Cnossen, J.S.2
Langejans, M.3
Robson, S.C.4
Kleijnen, J.5
Ter Riet, G.6
Mol, B.W.7
Van Der Post, J.A.8
Khan, K.S.9
-
37
-
-
84891664233
-
Costs and outcomes of noninvasive prenatal testing for down syndrome
-
Morris S, Karlsen S, Chung N, Hill M, Chitty LS (2013) Costs and outcomes of noninvasive prenatal testing for Down syndrome. Prenatal Diagnosis 33(Supplement 1): 6
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.SUPPL. 1
, pp. 6
-
-
Morris, S.1
Karlsen, S.2
Chung, N.3
Hill, M.4
Chitty, L.S.5
-
38
-
-
84902202209
-
-
NHS Fetal Anomaly Screening Programme, Annual report 2011-2012. NHS FASP, Exeter
-
NHS Fetal Anomaly Screening Programme (2012) NHS Fetal Anomaly Screening Programme. Annual report 2011-2012. NHS FASP, Exeter
-
(2012)
NHS Fetal Anomaly Screening Programme.
-
-
-
39
-
-
78650803485
-
Screening for fetal aneuploidies at 11 to 13 weeks
-
Nicolaides KH (2011) Screening for fetal aneuploidies at 11 to 13 weeks. Prenatal Diagnosis 31(7): 7-15
-
(2011)
Prenatal Diagnosis
, vol.31
, Issue.7
, pp. 7-15
-
-
Nicolaides, K.H.1
-
40
-
-
84868029481
-
Non-invasive prenatal testing for fetal trisomies in a routinely screened first-trimester population
-
e-6
-
Nicolaides KH, Syngelaki A, Ashoor G, Birdir C, Touzet G (2012) Non-invasive prenatal testing for fetal trisomies in a routinely screened first-trimester population. American Journal of Obstetrics and Gynecology 207(5): 374 e-6
-
(2012)
American Journal of Obstetrics and Gynecology
, vol.207
, Issue.5
, pp. 374
-
-
Nicolaides, K.H.1
Syngelaki, A.2
Ashoor, G.3
Birdir, C.4
Touzet, G.5
-
41
-
-
84878164024
-
Validation of targeted sequencing of singlenucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, x, and y
-
Nicolaides H, Syngelaki A, Gil M, Atanasova V, Markova D (2013) Validation of targeted sequencing of singlenucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y. Prenatal Diagnosis 33(6): 575-9
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 575-579
-
-
Nicolaides, H.1
Syngelaki, A.2
Gil, M.3
Atanasova, V.4
Markova, D.5
-
42
-
-
84864408781
-
Non-invasive chromosomal evaluation (nice) study: Results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18
-
e1-8
-
Norton ME, Brar H, Weiss J, Karimi A, Laurent LC, Caughey AB, Rodriguez MH, Williams J 3rd, Mitchell ME, Adair CD, Lee H, Jacobsson B, Tomlinson MW, Oepkes D, Hollemon D, Sparks AB, Oliphant A, Song K (2012) Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. American Journal of Obstetetrics and Gynecology 207(2): 137 e1-8
-
(2012)
American Journal of Obstetetrics and Gynecology
, vol.207
, Issue.2
, pp. 137
-
-
Norton, M.E.1
Brar, H.2
Weiss, J.3
Karimi, A.4
Laurent, L.C.5
Caughey, A.B.6
Rodriguez, M.H.7
Williams III, J.8
Mitchell, M.E.9
Adair, C.D.10
Lee, H.11
Jacobsson, B.12
Tomlinson, M.W.13
Oepkes, D.14
Hollemon, D.15
Sparks, A.B.16
Oliphant, A.17
Song, K.18
-
44
-
-
84874751049
-
Progress in prenatal genetic diagnosis: Using cell-free fetal dna in maternal blood
-
Oxenford K, Karunaratna M, Hill M, Taffinder S, Chitty L (2013) Progress in prenatal genetic diagnosis: Using cell-free fetal DNA in maternal blood. British Journal of Midwifery 21(2): 84-90
-
(2013)
British Journal of Midwifery
, vol.21
, Issue.2
, pp. 84-90
-
-
Oxenford, K.1
Karunaratna, M.2
Hill, M.3
Taffinder, S.4
Chitty, L.5
-
45
-
-
80755172331
-
Dna sequencing of maternal plasma to detect down syndrome: An international clinical validation study
-
Palomaki GE, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Deciu C, Grody WW, Nelson SF, Canick JA (2011) DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study. Genetics in Medicine 13(11): 913-20
-
(2011)
Genetics in Medicine
, vol.13
, Issue.11
, pp. 913-920
-
-
Palomaki, G.E.1
Kloza, E.M.2
Lambert-Messerlian, G.M.3
Haddow, J.E.4
Neveux, L.M.5
Ehrich, M.6
Van Den Boom, D.7
Bombard, A.T.8
Deciu, C.9
Grody, W.W.10
Nelson, S.F.11
Canick, J.A.12
-
46
-
-
84857868297
-
Dna sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as down syndrome: An international collaborative study
-
Palomaki GE, Deciu C, Kloza EM, Lambert-Messerlian GM, Haddow JE, Neveux LM, Ehrich M, van den Boom D, Bombard AT, Grody WW, Nelson SF, Canick JA (2012) DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: An international collaborative study. Genetics in Medicine 14(3): 296-305
-
(2012)
Genetics in Medicine
, vol.14
, Issue.3
, pp. 296-305
-
-
Palomaki, G.E.1
Deciu, C.2
Kloza, E.M.3
Lambert-Messerlian, G.M.4
Haddow, J.E.5
Neveux, L.M.6
Ehrich, M.7
Van Den Boom, D.8
Bombard, A.T.9
Grody, W.W.10
Nelson, S.F.11
Canick, J.A.12
-
47
-
-
84878123682
-
Discordant results between fetal karyotyping and noninvasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue
-
Pan M, Li FT, Li Y, Jiang FM, Li DZ, Lau TK, Liao C (2013) Discordant results between fetal karyotyping and noninvasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue. Prenatal Diagnosis 33(6): 598-601
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 598-601
-
-
Pan, M.1
Li, F.T.2
Li, Y.3
Jiang, F.M.4
Li, D.Z.5
Lau, T.K.6
Liao, C.7
-
48
-
-
80055084588
-
Cellfree fetal dna testing: A pilot study of obstetric healthcare provider attitudes toward clinical implementation
-
Sayres LC, Allyse M, Norton ME, Cho MK (2011) Cellfree fetal DNA testing: A pilot study of obstetric healthcare provider attitudes toward clinical implementation. Prenatal Diagnosis 31(11): 1070-6
-
(2011)
Prenatal Diagnosis
, vol.31
, Issue.11
, pp. 1070-1076
-
-
Sayres, L.C.1
Allyse, M.2
Norton, M.E.3
Cho, M.K.4
-
49
-
-
84862502335
-
Integrating stakeholder perspectives into the translation of cell-free fetal dna testing for aneuploidy
-
Sayres LC, Allyse M, Cho MK (2012) Integrating stakeholder perspectives into the translation of cell-free fetal DNA testing for aneuploidy. Genome Medicine 4(6): 49
-
(2012)
Genome Medicine
, vol.4
, Issue.6
, pp. 49
-
-
Sayres, L.C.1
Allyse, M.2
Cho, M.K.3
-
50
-
-
84878153039
-
Cell-free fetal dna sex determination identified a maternal sry gene with a known x chromosome deletion
-
Searle CJ, Smith K, Daniels G, Maher EJ, Quarrell O (2013) Cell-free fetal DNA sex determination identified a maternal SRY gene with a known X chromosome deletion. Prenatal Diagnosis 33(6): 612-3
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.6
, pp. 612-613
-
-
Searle, C.J.1
Smith, K.2
Daniels, G.3
Maher, E.J.4
Quarrell, O.5
-
51
-
-
59649122001
-
Prenatal screening for down syndrome: Women's involvement in decision-making and their attitudes to screening
-
Seror V, Ville Y (2009) Prenatal screening for Down syndrome: Women's involvement in decision-making and their attitudes to screening. Prenatal Diagnosis 29(2): 120-8
-
(2009)
Prenatal Diagnosis
, vol.29
, Issue.2
, pp. 120-128
-
-
Seror, V.1
Ville, Y.2
-
52
-
-
84857502701
-
Selective analysis of cellfree dna in maternal blood for evaluation of fetal trisomy
-
Sparks AB, Wang ET, Struble CA, Barrett W, Stokowski R, McBride C, Zahn J, Lee K, Shen N, Doshi J, Sun M, Garrison J, Sandler J, Hollemon D, Pattee P, Tomita-Mitchell A, Mitchell M, Stuelpnagel J, Song K, Oliphant A. (2012a) Selective analysis of cellfree DNA in maternal blood for evaluation of fetal trisomy. Prenatal Diagnosis 32(1): 3-9
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.1
, pp. 3-9
-
-
Sparks, A.B.1
Wang, E.T.2
Struble, C.A.3
Barrett, W.4
Stokowski, R.5
McBride, C.6
Zahn, J.7
Lee, K.8
Shen, N.9
Doshi, J.10
Sun, M.11
Garrison, J.12
Sandler, J.13
Hollemon, D.14
Pattee, P.15
Tomita-Mitchell, A.16
Mitchell, M.17
Stuelpnagel, J.18
Song, K.19
Oliphant, A.20
more..
-
53
-
-
84859361254
-
Non-invasive prenatal detection and selective analysis of cell-free dna obtained from maternal blood: Evaluation for trisomy 21 and trisomy 18
-
e1-9
-
Sparks AB, Struble CA, Wang ET, Song K, Oliphant A (2012b) Non-invasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18. American Journal of Obstetrics and Gynecology 206(4): 319 e1-9
-
(2012)
American Journal of Obstetrics and Gynecology
, vol.206
, Issue.4
, pp. 319
-
-
Sparks, A.B.1
Struble, C.A.2
Wang, E.T.3
Song, K.4
Oliphant, A.5
-
54
-
-
76449093190
-
Update on procedurerelated risks for prenatal diagnosis techniques
-
Tabor A, Alfirevic Z (2010) Update on procedurerelated risks for prenatal diagnosis techniques. Fetal Diagnosis and Therapy 27(1): 1-7
-
(2010)
Fetal Diagnosis and Therapy
, vol.27
, Issue.1
, pp. 1-7
-
-
Tabor, A.1
Alfirevic, Z.2
-
55
-
-
77953052466
-
Prenatal testing for down syndrome: Comparison of screening practices in the uk and usa
-
Tapon D (2010) Prenatal testing for Down syndrome: Comparison of screening practices in the UK and USA. Journal of Genetic Counselling 19(2): 112-30
-
(2010)
Journal of Genetic Counselling
, vol.19
, Issue.2
, pp. 112-130
-
-
Tapon, D.1
-
56
-
-
84891659808
-
Nipt in a clinical setting: An analysis of uptake in the first months of clinical availability
-
[Epub ahead of print]
-
Taylor B, Chock VY, Hudgins L (2013) NIPT in a clinical setting: an analysis of uptake in the first months of clinical availability. Journal of Genetic Counselling [Epub ahead of print]
-
(2013)
Journal of Genetic Counselling
-
-
Taylor, B.1
Chock, V.Y.2
Hudgins, L.3
-
57
-
-
82255192286
-
Noninvasive prenatal diagnosis: Pregnant women's interest and expected uptake
-
Tischler R, Hudgins L, Blumenfeld YJ, Greely HT, Ormond KE (2011) Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake. Prenatal Diagnosis 31(13): 1292-9
-
(2011)
Prenatal Diagnosis
, vol.31
, Issue.13
, pp. 1292-1299
-
-
Tischler, R.1
Hudgins, L.2
Blumenfeld, Y.J.3
Greely, H.T.4
Ormond, K.E.5
-
58
-
-
84891661216
-
Non-invasive prenatal testing for down syndrome
-
Twiss P, Hill M, Daley R, Chitty LS (2014) Non-invasive prenatal testing for Down syndrome. Seminars in Fetal and Neonatal Medicine 19(1): 9-14
-
(2014)
Seminars in Fetal and Neonatal Medicine
, vol.19
, Issue.1
, pp. 9-14
-
-
Twiss, P.1
Hill, M.2
Daley, R.3
Chitty, L.S.4
-
59
-
-
84918563011
-
-
UK Clinical Research Network, public.ukcrn.org.uk/search/StudyDetail. aspx?StudyID=13865 (accessed 13 January 2013
-
UK Clinical Research Network (2013a) NIPT for aneuploidy evaluation study. public.ukcrn.org.uk/search/StudyDetail. aspx?StudyID=13865 (accessed 13 January 2013)
-
(2013)
NIPT for Aneuploidy Evaluation Study
-
-
-
60
-
-
84902200499
-
-
UK Clinical Research Network. public.ukcrn.org.uk/Search/StudyDetail. aspx?StudyID=15084 (accessed 13 January 2013
-
UK Clinical Research Network (2013a) First-trimester cfDNA Testing. public.ukcrn.org.uk/Search/StudyDetail. aspx?StudyID=15084 (accessed 13 January 2013)
-
(2013)
First-Trimester cfDNA Testing
-
-
-
63
-
-
84889638841
-
Patient acceptance of non-invasive testing for fetal aneuploidy via cell-free fetal dna
-
Vahanian SA, Allaf MB, Yeh C, Chavez MR, Kinzler WL, Vintzileos AM (2014) Patient acceptance of non-invasive testing for fetal aneuploidy via cell-free fetal DNA. Journal of Maternal-Fetal and Neonatal Medicine 27(1): 106-9
-
(2014)
Journal of Maternal-Fetal and Neonatal Medicine
, vol.27
, Issue.1
, pp. 106-109
-
-
Vahanian, S.A.1
Allaf, M.B.2
Yeh, C.3
Chavez, M.R.4
Kinzler, W.L.5
Vintzileos, A.M.6
-
64
-
-
20444494910
-
Are pregnant women making informed choices about prenatal screening?
-
DOI 10.1097/01.GIM.0000162876.65555.AB
-
van den Berg M, Timmermans DR, Ten Kate LP, van Vugt JM, van der Wal G (2005) Are pregnant women making informed choices about prenatal screening? Genetics in Medicine 7(5): 332-8 (Pubitemid 40827582)
-
(2005)
Genetics in Medicine
, vol.7
, Issue.5
, pp. 332-338
-
-
Van Den Berg, M.1
Timmermans, D.R.M.2
Ten Kate, L.P.3
Van Vugt, J.M.G.4
Van Der Wal, G.5
-
65
-
-
84875179556
-
Incorporating dna sequencing into current prenatal screening practice for down's syndrome
-
Wald NJ, Bestwick JP (2013) Incorporating DNA sequencing into current prenatal screening practice for Down's syndrome. PLoS One 8(3): e58732
-
(2013)
PLoS One
, vol.8
, Issue.3
-
-
Wald, N.J.1
Bestwick, J.P.2
-
66
-
-
84880043573
-
Gestational age and maternal weight effects on fetal cell-free dna in maternal plasma
-
Wang E, Batey A, Struble C, Musci T, Song K, Oliphant A (2013) Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma. Prenatal Diagnosis 33(7): 662-6
-
(2013)
Prenatal Diagnosis
, vol.33
, Issue.7
, pp. 662-666
-
-
Wang, E.1
Batey, A.2
Struble, C.3
Musci, T.4
Song, K.5
Oliphant, A.6
-
67
-
-
84870695892
-
Non-invasive prenatal aneuploidy testing of chromosomes 13, 18, 21, x, and y, using targeted sequencing of polymorphic loci
-
Zimmermann B, Hill M, Gemelos G, Demko Z, Banjevic M, Baner J, Ryan A, Sigurjonsson S, Chopra N, Dodd M, Levy B, Rabinowitz M (2012) Non-invasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci. Prenatal Diagnosis 32(13): 1233-41
-
(2012)
Prenatal Diagnosis
, vol.32
, Issue.13
, pp. 1233-1241
-
-
Zimmermann, B.1
Hill, M.2
Gemelos, G.3
Demko, Z.4
Banjevic, M.5
Baner, J.6
Ryan, A.7
Sigurjonsson, S.8
Chopra, N.9
Dodd, M.10
Levy, B.11
Rabinowitz, M.12
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