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Bernd Eiben
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23
Hammans, W
21
Goebel, R
8
Epplen, JT
6
Louwen, Frank
6
Trawicki, W
5
Bartels, Iris
3
Osmers, Rüdiger
2
Miny, Peter
2
Sancken, Ulrich
2
Engel, Wolfgang
2
Horst, Jürgen
1
Kennerknecht, Ingo
1
Knudsen, G P S
1
Kunz, Jürgen
1
Marteau, Theresa
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Geonetwork of Bernd Eiben (preview)
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All Publications
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2005: Fritz Barbara; Kunz Jürgen; Knudsen Gun Peggy Strømstad; Louwen Frank; Kennerknecht Ingo; Eiben Bernd; Orstavik Karen Helene; Friedrich Ursula; Rehder Helga
Situs ambiguus in a female fetus with balanced (X;21) translocation--evidence for functional nullisomy of the ZIC3 gene?
European journal of human genetics : EJHG 2005;13(1):34-40.
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2002: Marteau Theresa M; Nippert Irma; Hall Sue; Limbert Caroline; Reid Margaret; Bobrow Martin; Cameron Alan; Cornel Martina; van Diem Mariet; Eiben Bernd; García-Miñaur Sixto; Goujard Janine; Kirwan Donna; McIntosh Karen; Soothill Peter; Verschuuren-Bemelmans Corien; de Vigan Catherine; Walkinshaw Stephen; Abramsky Lenore; Louwen Frank; Miny Peter; Horst Jürgen;
Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals.
Prenatal diagnosis 2002;22(7):562-6.
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2001: Eiben B; Hammans W; Keuter S; Goebel R; Louwen F; Epplen J
[Clinical study of assessment of trisomy 21--precise risk evaluation in the first trimester of pregnancy]
Zeitschrift für Geburtshilfe und Neonatologie 2001;205(3):94-8.
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2000: Eiben B; Goebel R; von Kaisenberg C; Hammans W; Epplen J T
[A new test to estimate risk for chromosomal trisomy in the first pregnancy trimester]
Deutsche medizinische Wochenschrift (1946) 2000;125(39):1173-7.
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2000: Eiben B; Hammans W; Keuter S; Goebel R; Louwen F; Epplen J T
Maternal serum total hCG and free beta-hCG in the first trimester from trisomy 21 pregnancies.
Prenatal diagnosis 2000;20(9):770-2.
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2000: Held K; Eiben B; Miny P
The long-term effect of external quality assessment on performance in service cytogenetics.
Cytogenetics and cell genetics 2000;91(1-4):124-7.
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1999: Sancken U; Bartels I; Louwen F; Eiben B
A retrospective evaluation of second-trimester serum screening for fetal trisomy 18: experience of two laboratories.
Prenatal diagnosis 1999;19(10):947-54.
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1999: Eiben B; Trawicki W; Hammans W; Epplen J T
False-negative finding in rapid interphase FISH analysis of uncultured amniotic cells.
Prenatal diagnosis 1999;19(9):892-3.
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1999: Eiben B; Trawicki W; Hammans W; Goebel R; Pruggmayer M; Epplen J T
Rapid prenatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Evaluation of >3,000 cases.
Fetal diagnosis and therapy 1999;14(4):193-7.
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1998: Eiben B; Trawicki W; Hammans W; Goebel R; Epplen J T
A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis.
Prenatal diagnosis 1998;18(9):901-6.
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1998: Eiben B; Hammans W; Goebel R; Epplen J T
Safety and fetal outcome of early and midtrimester amniocentesis.
Lancet 1998;351(9113):1435; author reply 1435-6.
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1998: Eiben B; Hammans W; Trawicki W; Goebel R
Early amniocentesis versus chorionic villus sampling.
Prenatal diagnosis 1998;18(4):405-7.
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1998: Eiben B; Trawicki W; Haupt A; Kasper S; Wenger D; Baier B; Hammans W
Discordant karyotypes in CVS and amniocenteses using cytogenetic and fluorescence in situ hybridization (FISH) analyses.
Prenatal diagnosis 1998;18(1):87-9.
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1998: Eiben B; Hammans W; Goebel R; Epplen J T
[A new rapid test (FISH) for the prenatal diagnosis of the most frequent chromosome aberrations--what significance has it in practice?]
Deutsche medizinische Wochenschrift (1946) 1998;123(3):55-7.
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1997: Eiben B; Hammans W; Goebel R
Chorionic villus sampling versus early amniocentesis.
Lancet 1997;350(9086):1253-4.
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1997: Meschede D; Louwen F; Eiben B; Horst J
Intracytoplasmic sperm injection pregnancy with fetal trisomy 9p resulting from a balanced paternal translocation.
Human reproduction (Oxford, England) 1997;12(9):1913-4.
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1997: Eiben B; Hammans W; Hansen S; Trawicki W; Osthelder B; Stelzer A; Jaspers K D; Goebel R
On the complication risk of early amniocentesis versus standard amniocentesis.
Fetal diagnosis and therapy 1997;12(3):140-4.
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1996: Eiben B; Sancken U
Computer software programs and Down's syndrome risk calculations.
Lancet 1996;347(9014):1553-4.
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1996: Eiben B; Hammans W; Goebel R
Triploidy, imprinting, and hCG levels in maternal serum screening.
Prenatal diagnosis 1996;16(4):377-8.
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1996: Eiben B; Goebel R; Hansen S; Hammans W
Alpha-fetoprotein and AChE in early amniocentesis.
Prenatal diagnosis 1996;16(1):87-8.
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1994: Eiben B; Osthelder B; Hammans W; Goebel R
Safety of early amniocentesis versus CVS.
Lancet 1994;344(8932):1303-4.
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1994: Caspari D; Bartels I; Rauskolb R; Prange G; Osmers R; Eiben B
Discrepant karyotypes after second- and third-trimester combined placentacentesis/amniocentesis.
Prenatal diagnosis 1994;14(7):569-76.
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1994: Eiben B; Goebel R; Hansen S; Hammans W
Early amniocentesis--a cytogenetic evaluation of over 1500 cases.
Prenatal diagnosis 1994;14(6):497-501.
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1993: Eiben B; Goebel R; Rutt G; Jaspers K D; Hansen S; Hammans W
[Early amniocentesis between the 12th-14th week of pregnancy. Clinical experiences with 1,100 cases]
Geburtshilfe und Frauenheilkunde 1993;53(8):554-8.
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1993: Eiben B; Hammans W; Goebel R
Fetal development after chorionic villus sampling.
Lancet 1993;341(8851):1037-8.
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1992: Eiben B; Unger M; Stoltenberg G; Rutt G; Goebel R; Meyer A; Gamerdinger U; Hammans W; Hansen S; Hauss H
Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism.
Prenatal diagnosis 1992;12(11):945-50.
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1992: Pruggmayer M R; Jahoda M G; Van der Pol J G; Baumann P; Holzgreve W; Karkut G; Lettau R; Eiben B; Osmers R; Gola H W; Duda V; Polak P; Körner H; Schulte-Valentin M; Schütte H
Genetic amniocentesis in twin pregnancies: results of a multicenter study of 529 cases.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 1992;2(1):6-10.
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1991: Eiben B; Goebel R
[Clinical experience and possibilities of rapid cytogenetic diagnosis of spontaneous abortions in the routine work load of a gynecology clinic]
Geburtshilfe und Frauenheilkunde 1991;51(6):450-3.
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1990: Eiben B; Bartels I; Bähr-Porsch S; Borgmann S; Gatz G; Gellert G; Goebel R; Hammans W; Hentemann M; Osmers R
Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage.
American journal of human genetics 1990;47(4):656-63.
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1990: Gatz G; Rauskolb R; Werner L; Gellert G; Eiben B; Bartels I
Simultaneous placentacentesis and amniocentesis for prenatal karyotyping: report on 250 cases.
Prenatal diagnosis 1990;10(6):365-75.
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1990: Bartels I; Hansmann I; Eiben B
Excess of females in chromosomally normal spontaneous abortuses.
American journal of medical genetics 1990;35(2):297-8.
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1989: Eiben B; Hansen S; Goebel R; Hammans W
Tissue-specific 45,X0/47,XY,+13 mosaicism in an 18-year-old woman.
Human genetics 1989;82(4):391-2.
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1989: Minguillon C; Eiben B; Bähr-Porsch S; Vogel M; Hansmann I
The predictive value of chorionic villus histology for identifying chromosomally normal and abnormal spontaneous abortions.
Human genetics 1989;82(4):373-6.
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1989: Eiben B; Hansen S; Knipping J; Massenberg R; Goebel R; Hammans W
Translocation trisomy 21 in CVS not found in embryoblast: three different cell lines in CVS, amnion- and placental culture.
Prenatal diagnosis 1989;9(5):365-7.
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1988: Bernert J; Rauskolb R; Jovanovic V; Eiben B; Hansmann I; Mevatee U; Schleiermacher E; Köhler A
[Cytogenetic studies of chorionic villi tissue of abortion samples]
Der Gynäkologe 1988;21(2):107-9.
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1988: Eiben B; Hammans W; Hansen S
Chromosomal rearrangement involving chromosomes 4, 6, 11 and 11.
Human genetics 1988;79(2):193.
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1988: Eiben B; Leipoldt M; Schübbe I; Ulbrich R; Hansmann I
Partial deletion of 4p in fetal cells not present in chorionic villi.
Clinical genetics 1988;33(1):49-52.
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1987: Eiben B; Leipoldt M; Rammelsberg O; Krause W; Engel W
High incidence of minor chromosomal variants in teratozoospermic males.
Andrologia 1987;19(6):684-7.
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1987: Eiben B; Borgmann S; Schübbe I; Hansmann I
A cytogenetic study directly from chorionic villi of 140 spontaneous abortions.
Human genetics 1987;77(2):137-41.
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1987: Leipoldt M; Eiben B; Krause W; Engel W
Nekrozoospermia in mosaic Klinefelter's syndrome.
Andrologia 1987;19(2):175-7.
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1986: Eiben B; Schübbe I; Borgmann S; Hansmann I
Rapid cytogenetic diagnosis of early spontaneous abortions.
Lancet 1986;1(8492):1273-4.
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