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John Philip
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20
Lundsteen, Claes
18
Bang, Jens
13
Bryndorf, Thue
9
Christensen, Britta
6
Kølvraa, Steen
6
Sundberg, Karin
5
Smidt-Jensen, Steen
5
Lykke-Hansen, Lene
5
Xiang, Yang
4
Gerdes, Tommy
4
Nørgaard-Pedersen, Bent
3
Pergament, Eugene
3
Platt, Lawrence
3
Filkins, Karen
3
Mahoney, Maurice
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All Publications
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2005: Philip John; Christensen Britta; Kølvraa Steen
[The fetal erythroblast is not the optimal target for non-invasive prenatal diagnosis--secondary publication]
Ugeskrift for laeger 2005;167(15):1644-6.
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2005: Philip J; Silver R K; Wilson R D; Thom E A; Zachary J M; Mohide P; Mahoney M J; Simpson J L; Platt L D; Pergament E; Hershey D; Filkins K; Johnson A; Shulman L P; Bang J; MacGregor S; Smith J R; Shaw D; Wapner R J; Jackson L G;
[Late first-trimester invasive prenatal diagnosis--secondary publication. An international randomized trial]
Ugeskrift for laeger 2005;167(11):1293-6.
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2005: Kølvraa Steen; Christensen Britta; Lykke-Hansen Lene; Philip John
The fetal erythroblast is not the optimal target for non-invasive prenatal diagnosis: preliminary results.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):331-6.
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2005: Silver Richard K; Wilson R Douglas; Philip John; Thom Elizabeth A; Zachary Julia M; Mohide Patrick; Mahoney Maurice J; Simpson Joe L; Platt Larry D; Pergament Eugene; Hershey Douglas; Filkins Karen; Johnson Anthony; Wapner Ronald J; Jackson Laird G;
Late first-trimester placental disruption and subsequent gestational hypertension/preeclampsia.
Obstetrics and gynecology 2005;105(3):587-92.
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2005: Christensen Britta; Philip John; Kølvraa Steen; Lykke-Hansen Lene; Hromadnikova Ilona; Gohel Dhanesh; Lorch Thomas; Plesch Andreas; Bang Jens; Smidt-Jensen Steen; Hertz Jens; Djursing Henning
Fetal cells in maternal blood: a comparison of methods for cell isolation and identification.
Fetal diagnosis and therapy 2005;20(2):106-12.
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2004: Philip J; Silver R K; Wilson R D; Thom E A; Zachary J M; Mohide P; Mahoney M J; Simpson J L; Platt L D; Pergament E; Hershey D; Filkins K; Johnson A; Shulman L P; Bang J; MacGregor S; Smith J R; Shaw D; Wapner R J; Jackson L G;
Late first-trimester invasive prenatal diagnosis: results of an international randomized trial.
Obstetrics and gynecology 2004;103(6):1164-73.
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2003: Philip John; Christensen Britta; Kølvraa Steen; Lykke-Hansen Lene; Bang Jens; Smidt-Jensen Steen; Egebart Jonas; Hertz Jens
[Fetal cells in the pregnant woman's blood as material for fetal diagnosis]
Ugeskrift for laeger 2003;165(46):4382-4.
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2003: Christensen Britta; Philip John; Lykke-Hansen Lene; Kølvraa Steen
Sensitivity and specificity of the identification of fetal cells in maternal blood by combined staining with antibodies against beta-, gamma- and epsilon-globin chains.
Fetal diagnosis and therapy 2003;18(6):479-84.
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2003: Christensen B; Kølvraa S; Lykke-Hansen L; Lörch T; Gohel D; Smidt-Jensen S; Bang J; Philip J
Studies on the isolation and identification of fetal nucleated red blood cells in the circulation of pregnant women before and after chorion villus sampling.
Fetal diagnosis and therapy 2003;18(5):376-84.
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2002: Meyer Annette; Lundsteen Claes; Philip John
[Evaluation by pregnant women of prenatal counseling. A quality assurance project]
Ugeskrift for laeger 2002;164(9):1220-3.
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2001: Høgh A M; Hviid T V; Christensen B; Sørensen S; Larsen R D; Smidt-Jensen S; Bang J; Philip J
zeta-, epsilon-, and gamma-Globin mRNA in blood samples and CD71(+) cell fractions from fetuses and from pregnant and nonpregnant women, with special attention to identification of fetal erythroblasts.
Clinical chemistry 2001;47(4):645-53.
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2000: Bryndorf T; Lundsteen C; Lamb A; Christensen B; Philip J
Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
Acta obstetricia et gynecologica Scandinavica 2000;79(1):8-14.
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1999: Friis-Hansen L J; Gøtze J P; Philip J
[Pregnancy complications and thrombophilia]
Ugeskrift for laeger 1999;161(36):5034.
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1999: Jørgensen F S; Valentin L; Salvesen K A; Jørgensen C; Jensen F R; Bang J; Eik-Nes S H; Madsen M; Marsal K; Persson P H; Philip J; Bogstad J W; Nørgaard-Pedersen B
MULTISCAN--a Scandinavian multicenter second trimester obstetric ultrasound and serum screening study.
Acta obstetricia et gynecologica Scandinavica 1999;78(6):501-10.
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1999: Sundberg K; Lundsteen C; Philip J
Comparison of cell cultures, chromosome quality and karyotypes obtained after chorionic villus sampling and early amniocentesis with filter technique.
Prenatal diagnosis 1999;19(1):12-6.
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1998: Philip J
[Papillomavirus, uterine cervix cancer and screening]
Ugeskrift for laeger 1998;160(50):7275.
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1997: Sundberg K; Bang J; Smidt-Jensen S; Brocks V; Lundsteen C; Parner J; Keiding N; Philip J
Randomised study of risk of fetal loss related to early amniocentesis versus chorionic villus sampling.
Lancet 1997;350(9079):697-703.
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1997: Bryndorf T; Christensen B; Vad M; Parner J; Brocks V; Philip J
Prenatal detection of chromosome aneuploidies by fluorescence in situ hybridization: experience with 2000 uncultured amniotic fluid samples in a prospective preclinical trial.
Prenatal diagnosis 1997;17(4):333-41.
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1996: Sundberg K; Lundsteen C; Philip J
Early filtration amniocentesis for further investigation of mosaicism diagnosed by chorionic villus sampling.
Prenatal diagnosis 1996;16(12):1121-7.
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1996: Bryndorf T; Christensen B; Vad M; Parner J; Carelli M P; Ward B E; Klinger K W; Bang J; Philip J
Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISH.
American journal of human genetics 1996;59(4):918-26.
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1996: Philip J; Obel E B
[Supplementation of estrogen and progesterone to postmenopausal women]
Ugeskrift for laeger 1996;158(21):2998.
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1995: Philip J
[Pregnancy is a natural phenomenon! What about the risk factors?]
Ugeskrift for laeger 1995;157(51):7154-5.
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1995: Bryndorf T; Kirchhoff M; Rose H; Maahr J; Gerdes T; Karhu R; Kallioniemi A; Christensen B; Lundsteen C; Philip J
Comparative genomic hybridization in clinical cytogenetics.
American journal of human genetics 1995;57(5):1211-20.
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1995: Sundberg K; Bang J; Brocks V; Jensen F R; Smidt-Jensen S; Philip J
Early sonographically guided amniocenteses with filtration technique: follow-up on 249 procedures.
Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine 1995;14(8):585-90.
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1995: Xiang Y; Bryndorf T; Philip J; Sun N
[Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)]
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae 1995;17(2):120-4.
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1994: Philip J; Bryndorf T; Christensen B
Prenatal aneuploidy detection in interphase cells by fluorescence in situ hybridization (FISH).
Prenatal diagnosis 1994;14(13):1203-15.
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1994: Bryndorf T; Christensen B; Xiang Y; Philip J
Prenatal diagnosis by fluorescence in situ hybridization on chorionic villus cells: nonsignificance of maternal cell contamination.
Fetal diagnosis and therapy 1994;9(2):73-6.
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1994: Bryndorf T; Sundberg K; Christensen B; Philip J; Yokobata K; Gaiser C
Early and rapid prenatal exclusion of Down's syndrome.
Lancet 1994;343(8900):802.
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1994: Bryndorf T; Christensen B; Xiang Y; Philip J; Yokobata K; Bui N; Gaiser C
Fluorescence in situ hybridization with a chromosome 21-specific cosmid contig: 1-day detection of trisomy 21 in uncultured mesenchymal chorionic villus cells.
Prenatal diagnosis 1994;14(2):87-96.
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1994: Smidt-Jensen S; Philip J; Zachary J M; Fowler S E; Nørgaard-Pedersen B
Implications of maternal serum alpha-fetoprotein elevation caused by transabdominal and transcervical CVS.
Prenatal diagnosis 1994;14(1):35-45.
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1993: Sundberg K; Smidt-Jensen S; Lundsteen C; Agerbaek K; Philip J
Filtration and recirculation of early amniotic fluid. Evaluation of cell cultures from 100 diagnostic cases.
Prenatal diagnosis 1993;13(12):1101-10.
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1993: Jørgensen F S; Bang J; Lind A M; Christensen B; Lundsteen C; Philip J
[Early amniocentesis]
Ugeskrift for laeger 1993;155(40):3207-10.
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1993: Smidt-Jensen S; Lundsteen C; Lind A M; Dinesen K; Philip J
Transabdominal chorionic villus sampling in the second and third trimesters of pregnancy: chromosome quality, reporting time, and feto-maternal bleeding.
Prenatal diagnosis 1993;13(10):957-69.
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1993: Bryndorf T; Christensen B; Xiang Y; Lind A M; Philip J
Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells.
Prenatal diagnosis 1993;13(9):815-23.
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1993: Bagger P V; Andersen V; Baslund B; Beck B; Hove H; Høier-Madsen M; Petersen J; Philip J; Schaadt O; Skouby S O
Anti-cardiolipin antibodies (IgG and IgA) in women with recurrent fetal loss correlate to clinical and serological characteristics of SLE.
Acta obstetricia et gynecologica Scandinavica 1993;72(6):465-9.
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1993: Smidt-Jensen S; Lind A M; Permin M; Zachary J M; Lundsteen C; Philip J
Cytogenetic analysis of 2928 CVS samples and 1075 amniocenteses from randomized studies.
Prenatal diagnosis 1993;13(8):723-40.
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1993: Christensen B; Bryndorf T; Philip J; Xiang Y; Hansen W
Prenatal diagnosis by in situ hybridization on uncultured amniocytes: reduced sensitivity and potential risk of misdiagnosis in blood-stained samples.
Prenatal diagnosis 1993;13(7):581-7.
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1993: Philip J
Prevention of cervical cancer by screening.
Acta obstetricia et gynecologica Scandinavica 1993;72(4):236-7.
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1993: Philip J
[Methods for sampling of biological material for prenatal diagnosis of congenital diseases]
Ugeskrift for laeger 1993;155(19):1479-80.
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1993: Smidt-Jensen S L; Permin M; Philip J; Lundsteen C; Grüning L K; Zachary J M; Fowler S E
[Randomized comparison of transabdominal, transcervical chorionic villi sampling and amniocentesis]
Ugeskrift for laeger 1993;155(19):1446-56.
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1992: Smidt-Jensen S; Permin M; Philip J; Lundsteen C; Zachary J M; Fowler S E; Grüning K
Randomised comparison of amniocentesis and transabdominal and transcervical chorionic villus sampling.
Lancet 1992;340(8830):1237-44.
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1992: Bryndorf T; Christensen B; Philip J; Hansen W; Yokobata K; Bui N; Gaiser C
New rapid test for prenatal detection of trisomy 21 (Down's syndrome): preliminary report.
BMJ (Clinical research ed.) 1992;304(6841):1536-9.
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1992: Bryndorf T E; Christensen B; Philip J
[Non-radioactive in situ hybridization with chromosome-specific probes]
Ugeskrift for laeger 1992;154(21):1487-91.
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1992: Jørgensen F S; Bang J; Lind A M; Christensen B; Lundsteen C; Philip J
Genetic amniocentesis at 7-14 weeks of gestation.
Prenatal diagnosis 1992;12(4):277-83.
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1992: Christensen B; Bryndorf T; Philip J; Lundsteen C; Hansen W
Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization.
Prenatal diagnosis 1992;12(4):241-50.
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1991: Smidt-Jensen S; Philip J
Comparison of transabdominal and transcervical CVS and amniocentesis: sampling success and risk.
Prenatal diagnosis 1991;11(8):529-37.
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1991: Sundberg K; Smidt-Jensen S; Philip J
Amniocentesis with increased cell yield, obtained by filtration and reinjection of the amniotic fluid.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1991;1(2):91-4.
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1991: Smidt-Jensen S; Permin M; Philip J
Sampling success and risk by transabdominal chorionic villus sampling, transcervical chorionic villus sampling and amniocentesis: a randomized study.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1991;1(2):86-90.
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1991: Philip J; Smidt-Jensen S; Hilden J
The safety of chorionic villus sampling. A synthesis of the literature.
Annals of the New York Academy of Sciences 1991;626():568-79.
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1990: Goldstein H; Philip J
A cost-benefit analysis of prenatal diagnosis by amniocentesis in Denmark.
Clinical genetics 1990;37(4):241-63.
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1990: Holst K; Hilden J; Philip J; Andersen E; Goldstein H; Henningsen I
Which types of perinatal events are predictable? A look at a risk score model.
Acta obstetricia et gynecologica Scandinavica 1990;69(5):379-88.
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1989: Lundsteen C; Philip J
Automated cytogenetic analysis: accomplishments, present status and practical future possibilities.
Clinical genetics 1989;36(5):386-91.
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1989: Holst K; Andersen E; Philip J; Henningsen I
Antenatal and perinatal conditions correlated to handicap among 4-year-old children.
American journal of perinatology 1989;6(2):258-67.
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1988: Tabor A; Philip J; Bang J; Madsen M; Obel E B; Nørgaard-Pedersen B
Safety of amniocentesis.
Prenatal diagnosis 1988;8(2):167-8.
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1988: Tabor A; Philip J; Bang J; Madsen M; Obel E B; Nørgaard-Pedersen B
Needle size and risk of miscarriage after amniocentesis.
Lancet 1988;1(8578):183-4.
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1987: Lundsteen C; Gerdes T; Maahr J; Philip J
Clinical performance of a system for semiautomated chromosome analysis.
American journal of human genetics 1987;41(3):493-502.
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1987: Lundsteen C; Gerdes T; Maahr J; Philip J
[Automatic chromosome analysis in the routine laboratory]
Ugeskrift for laeger 1987;149(20):1329-32.
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1986: Tabor A; Philip J; Madsen M; Bang J; Obel E B; Nørgaard-Pedersen B
Randomised controlled trial of genetic amniocentesis in 4606 low-risk women.
Lancet 1986;1(8493):1287-93.
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1983: Philip J; Tabor A; Bang J; Madsen M
Fetal chromosome analysis: screening for chromosome disease?
Prenatal diagnosis 1983;3(3):209-18.
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1983: Palle C; Andersen J W; Tabor A; Lauritsen J G; Bang J; Philip J
Increased risk of abortion after genetic amniocentesis in twin pregnancies.
Prenatal diagnosis 1983;3(2):83-9.
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1981: Tabor A; Bang J; Philip J
45,X karyotype: may the diagnosis be suspected on ultrasonic examination in the second trimester of pregnancy?
Prenatal diagnosis 1981;1(4):281-3.
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1981: Lundsteen C; Gerdes T; Granum E; Philip J; Philip K
Automatic chromosome analysis. II. Karyotyping of banded human chromosomes using band transition sequences.
Clinical genetics 1981;19(1):26-36.
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1980: Lundsteen C; Philip J; Granum E
Quantitative analysis of 6985 digitized trypsin G-banded human metaphase chromosomes.
Clinical genetics 1980;18(5):355-70.
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1980: Lundsteen C; Bjerregaard B; Granum E; Philip J; Philip K
Automatic chromosome analysis. I. A simple method for classification of B- and D-group chromosomes represented by band transition sequences.
Clinical genetics 1980;17(3):183-90.
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