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1

Tailored 3D Mechanical Metamaterials Made by Dip-in Direct-Laser-Writing Optical Lithography

Tiemo Bückmann, Nicolas Stenger, Muamer Kadic, Johannes Kaschke, Andreas Frölich, Tobias Kennerknecht, Christoph Eberl, Michael Thiel, Martin Wegener

Journal:

Advanced Materials

Year:

2012

Language:

english

File:

PDF, 721 KB

english, 2012

2

Mechanical properties of bulk single crystalline nanoporous gold investigated by millimetre-scale tension and compression testing

Briot, Nicolas J., Kennerknecht, Tobias, Eberl, Christoph, Balk, T. John

Journal:

Philosophical Magazine

Year:

2014

Language:

english

File:

PDF, 906 KB

english, 2014

3

A computational model of dysfunctional facial encoding in congenital prosopagnosia

Rainer Stollhoff, Ingo Kennerknecht, Tobias Elze, Jürgen Jost

Journal:

Neural Networks

Year:

2011

Language:

english

File:

PDF, 1.06 MB

english, 2011

4

AUTOPSIE, ANATOMIE UND RECHTSMEDIZIN: CHINESISCHE QUELLEN ZUM MENSCHLICHEN KÖRPERBAU

Maria-Magdalena Kennerknecht-Hirth

Journal:

Monumenta Serica

Year:

2008

Language:

german

File:

PDF, 2.37 MB

german, 2008

5

First report of prevalence of non-syndromic hereditary prosopagnosia (HPA)

Ingo Kennerknecht, Thomas Grueter, Brigitte Welling, Sebastian Wentzek, Jürgen Horst, Steve Edwards, Martina Grueter

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 110 KB

english, 2006

6

Elastische Stabilität ebener Laminate

H. Bufler, H. Kennerknecht

Journal:

Archive of Applied Mechanics

Year:

1983

Language:

german

File:

PDF, 994 KB

german, 1983

7

Congenital prosopagnosia: multistage anatomical and functional deficits in face processing circuitry

V. Dinkelacker, M. Grüter, P. Klaver, T. Grüter, K. Specht, S. Weis, I. Kennerknecht, C. E. Elger, G. Fernandez

Journal:

Journal of Neurology

Year:

2011

Language:

english

File:

PDF, 541 KB

english, 2011

8

A cryptic insertion (17;15) on both chromosomes 17 with lack of PML–RARA expression in a case of atypical acute promyelocytic leukemia

Tchinda, J, Volpert, S, Liersch, R, Zühlsdorf, M, Serve, H, Neumann, T, Kennerknecht, I, Berdel, W E, Büchner, T, Horst, J

Journal:

Year:

2003

Language:

english

File:

PDF, 177 KB

english, 2003

9

Hereditary Prosopagnosia: the First Case Series

Martina Grueter, Thomas Grueter, Vaughan Bell, Juergen Horst, Wolfgang Laskowski, Karl Sperling, Peter W. Halligan, Hadyn D. Elli, Ingo Kennerknecht

Journal:

Year:

2007

Language:

english

File:

PDF, 216 KB

english, 2007

10

A family at risk: Congenital prosopagnosia, poor face recognition and visuoperceptual deficits within one family

Johnen, Andreas, Schmukle, Stefan C., Hüttenbrink, Judith, Kischka, Claudia, Kennerknecht, Ingo, Dobel, Christian

Journal:

Neuropsychologia

Year:

2014

Language:

english

File:

PDF, 967 KB

english, 2014

11

Influence of plate material on the contact strength of Li4SiO4 pebbles in crush tests and evaluation of the contact strength in pebble–pebble contact

Zhao, Shuo, Gan, Yixiang, Kamlah, Marc, Kennerknecht, Tobias, Rolli, Rolf

Journal:

Engineering Fracture Mechanics

Year:

2013

Language:

english

File:

PDF, 653 KB

english, 2013

12

Small-Scale Multiaxial Setup for Damage Detection Into the Very High Cycle Fatigue Regime

Straub, T., Berwind, M. F., Kennerknecht, T., Lapusta, Y., Eberl, C.

Journal:

Experimental Mechanics

Year:

2015

Language:

english

File:

PDF, 2.08 MB

english, 2015

13

A case of apparent trisomy 21 without the Down's syndrome phenotype.

Avramopoulos, D, Kennerknecht, I, Barbi, G, Eckert, D, Delabar, J M, Maunoury, C, Hallberg, A, Petersen, M B

Journal:

Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 1.08 MB

english, 1997

14

Galactose uncovers face recognition and mental images in congenital prosopagnosia: The first case report

Esins, Janina, Schultz, Johannes, Bülthoff, Isabelle, Kennerknecht, Ingo

Journal:

Nutritional Neuroscience

Year:

2014

Language:

english

File:

PDF, 90 KB

english, 2014

15

Morphological assessment of renal arteries after radiofrequency catheter-based sympathetic denervation in a porcine model

Steigerwald, Kristin, Titova, Anna, Malle, Caroline, Kennerknecht, Elisabeth, Jilek, Clemens, Hausleiter, Jörg, Nährig, Jörg M., Laugwitz, Karl-Ludwig, JONER, Michael

Journal:

Journal of Hypertension

Year:

2012

Language:

english

File:

PDF, 628 KB

english, 2012

16

Load Data Calculation in Electric Axle Drives and Fatigue Assessment for the Electric Motor Subsystem*

Knetsch, Dustin, Funk, Matthias, Kennerknecht, Tobias, Eberl, Christoph

Journal:

Materials Testing

Year:

2014

Language:

english

File:

PDF, 398 KB

english, 2014

17

Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome

Neuhaus, Christine, Eisenberger, Tobias, Decker, Christian, Nagl, Sandra, Blank, Cornelia, Pfister, Markus, Kennerknecht, Ingo, Müller-Hofstede, Cornelie, Charbel Issa, Peter, Heller, Raoul, Beck, Bod

Journal:

Molecular Genetics & Genomic Medicine

Year:

2017

Language:

english

File:

PDF, 3.62 MB

english, 2017

18

Long-lasting cough in an adult German population: incidence, symptoms, and related pathogens

Weinberger, Raphael, Riffelmann, Marion, Kennerknecht, Nicole, Hülße, Christel, Littmann, Martina, O’Brien, Judith, von Kries, Rüdiger, von König, Carl Heinz Wirsing

Journal:

European Journal of Clinical Microbiology & Infectious Diseases

Year:

2018

Language:

english

File:

PDF, 686 KB

english, 2018

19

Corrigendum: Do congenital prosopagnosia and the other-race effect affect the same face recognition mechanisms?

Esins, Janina, Schultz, Johannes, Stemper, Claudia, Kennerknecht, Ingo, Wallraven, Christian, BÃ¼lthoff, Isabelle

Journal:

Frontiers in Human Neuroscience

Year:

2015

Language:

english

File:

PDF, 168 KB

english, 2015

20

X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivation

Preis, Wolfgang, Barbi, Gotthold, Liptay, Susanne, Kennerknecht, Ingo, Schwemmle, Sabine, Pohlandt, Frank

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 558 KB

1996

21

XX-agonadism in a fetus with multiple dysraphic lesions: A new syndrome

Kennerknecht, Ingo, Mattfeldt, Torsten, Paulus, Wolfgang, Nitsch, Christian, Negri, Giovanni, Barbi, Gotthold, Just, Walter, Schwemmle, Sabine, Vogel, Walther

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 135 KB

english, 1997

22

Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype

Barbi, G., Kennerknecht, I., W�hr, G., Avramopoulos, D., Karadima, G., Petersen, M.B.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 265 KB

english, 2000

23

False-negative findings in chorionic villus sampling. An experimental approach and review of the literature

Ingo Kennerknecht, Gotthold Barbi, Mahmoud Djalali, Karl Mehnert, Michael Schneider, Rainer Terinde, Walther Vogel

Journal:

Prenatal Diagnosis

Year:

1998

Language:

english

File:

PDF, 152 KB

english, 1998

24

Author's response

Ingo Kennerknecht

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 100 KB

english, 1999

25

How can the frequency of false-negative findings in prenatal diagnoses of fra(X) be reduced: Experience with first trimester chorionic Villi sampling

Dr. Ingo Kennerknecht, Gotthold Barbi, Niklas Dahl, Peter Steinbach

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 566 KB

english, 1991

26

Reciprocal translocation t(1;15)(p36.2;p11.2): Confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)

Gotthold Barbi, Ingo Kennerknecht, Christine Klett

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 411 KB

english, 1992

27

Familial occurrence of agonadism and multiple internal malformations in phenotypically normal girls with 46,XY and 46,XX karyotypes, respectively: A new autosomal recessive syndrome

PD Dr. Ingo Kennerknecht, Wolfgang Sorgo, Renate Oberhoffer, Walter M. Teller, Torsten Mattfeldt, Giovanni Negri, Walther Vogel

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 635 KB

english, 1993

28

Dup(lq)(q42→qter) syndrome: Case report and review of literature

PD Dr. Ingo Kennerknecht, Gotthold Barbi, Klaus Rodens

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 347 KB

english, 1993

29

Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: A new autosomal recessive syndrome

Dr. Ingo Kennerknecht, Petra von Saurma, Rolf Brenner, Walter Just, Gotthold Barbi, Wolfgang Sorgo, Eberhard Heinze, Alfred S. Wolf, Volker Schneider, Klaus-Peter Günther, Walter M. Teller, Walther Vo

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 782 KB

english, 1995

30

Mild phenotype in two unrelated patients with a partial deletion of 21q22.2-q22.3 defined by FISH and molecular studies

Daniela Ehling, Ingo Kennerknecht, Annelore Junge, Bettina Prager, Rita Exeler, Beate Behre, Juergen Horst, Thomas Schmitt-John, Oliver Bartsch, Jutta Wirth

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 288 KB

english, 2004

31

Prevalence of hereditary prosopagnosia (HPA) in Hong Kong Chinese population

Ingo Kennerknecht, Nga Yee Ho, Prof. Virginia C.N. Wong

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 88 KB

english, 2008

32

Analytical and experimental investigations of the dynamic behaviour of the MAW evaporator module

Hans-Joachim Hilpert, Fritz-Otto Henkel, Helmut Kennerknecht

Journal:

Nuclear Engineering and Design

Year:

1991

Language:

english

File:

PDF, 595 KB

english, 1991

33

Criteria for the selection of significant load conditions for fatigue analysis demonstrated at a BWR RPV component

H. Kennerknecht, F.-O. Henkel

Journal:

International Journal of Pressure Vessels and Piping

Year:

1986

Language:

english

File:

PDF, 442 KB

english, 1986

34

Electron dynamics in a heterogeneous system: thin Ag films on Si(1 0 0)

Claudia Kennerknecht, Sandra Dantscher, Walter Pfeiffer, Olaf Autzen, Claudia Wesenberg, Eckart Hasselbrink

Journal:

Surface Science

Year:

2006

Language:

english

File:

PDF, 248 KB

english, 2006

35

Recurrent mutations in the COL1A2 gene in patients with osteogenesis imperfecta

T Trummer, R Brenner, W Just, W Vogel, I Kennerknecht

Journal:

Clinical Genetics

Year:

2001

Language:

english

File:

PDF, 106 KB

english, 2001

36

Intrauterine growth retardation associated with chromosomal aneuploidy confined to the placenta. Three observations: Triple trisomy 6,21,22; trisomy 16; and trisomy 18

Dr. I. Kennerknecht, R. Terinde

Journal:

Prenatal Diagnosis

Year:

1990

Language:

english

File:

PDF, 333 KB

english, 1990

37

Uncommon chromosomal mosaicism in chorionic villi

Dr. I. Kennerknecht, G. Barbi, M. Djalali, W. Just, W. Vogel, R. Terinde

Journal:

Prenatal Diagnosis

Year:

1991

Language:

english

File:

PDF, 481 KB

english, 1991

38

Proliferation kinetics in native chorionic villus cells

Dr. I. Kennerknecht, S. Baur-Aubele, W. Vogel

Journal:

Prenatal Diagnosis

Year:

1991

Language:

english

File:

PDF, 258 KB

english, 1991

39

First trimester amniocentesis between the seventh and 13th weeks: Evaluation of the earliest possible genetic diagnosis

Dr I. Kennerknecht, S. Baur-Aubele, D. Grab, R. Terinde

Journal:

Prenatal Diagnosis

Year:

1992

Language:

english

File:

PDF, 431 KB

english, 1992

40

Introduction of early amniocentesis to routine prenatal diagnosis

Dr M. Djalali, G. Barbi, I. Kennerknecht, R. Terinde

Journal:

Prenatal Diagnosis

Year:

1992

Language:

english

File:

PDF, 440 KB

english, 1992

41

Authors' reply

I. Kennerknecht, D. Grab, R. Terinde

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 93 KB

english, 1993

42

Evaluation of amniotic fluid cell filtration: An experimental approach to early amniocentesis

Dr Ingo Kennerknecht, Sabine Krämer, Dieter Grab, Rainer Terinde

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 569 KB

english, 1993

43

A prospective cytogenetic study of third-trimester placentae in small-for-date but otherwise normal newborns

Dr Ingo Kennerknecht, Sabine Krämer, Dieter Grab, Rainer Terinde, Walther Vogel

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 598 KB

english, 1993

44

A triploid fetus with a diploid placenta: Proposal of a mechanism

Ingo Kennerknecht, Walter Just, Walther Vogel

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 110 KB

english, 1993

45

Cytogenetic diagnoses after chorionic villus sampling are less reliable in very-high- or very-low-risk pregnancies

PD Dr Ingo Kennerknecht, Gotthold Barbi, Michael Wolf, Mahmoud Djalali, Dieter Grab, Rainer Terinde, Walther Vogel

Journal:

Prenatal Diagnosis

Year:

1993

Language:

english

File:

PDF, 972 KB

english, 1993

46

The gene coding for the α-chain of human propionyl-CoA carboxylase maps to chromosome band 13q32

I. Kennerknecht, T. Suormala, G. Barbi, E. R. Baumgartner

Journal:

Year:

1990

Language:

english

File:

PDF, 211 KB

english, 1990

47

Maternal transmission of ring chromosome 21

Ingo Kennerknecht, Gotthold Barbi, Walther Vogel

Journal:

Year:

1990

Language:

english

File:

PDF, 527 KB

english, 1990

48

Genotype mosaicism in fragile X fetal tissues

Doris Wöhrle, Mark C. Hirst, Ingo Kennerknecht, Kay E. Davies, Peter Steinbach

Journal:

Year:

1992

Language:

english

File:

PDF, 571 KB

english, 1992

49

A genetic model for the Prader-Willi syndrome and its implication for angelman syndrome

Ingo Kennerknecht

Journal:

Year:

1992

Language:

english

File:

PDF, 944 KB

english, 1992

50

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families

P. Steinbach, D. Wöhrle, G. Tariverdian, I. Kennerknecht, G. Barbi, H. Edlinger, H. Enders, M. Götz-Sothmann, H. Heilbronner, D. Hosenfeld, R. Kircheisen, F. Majewski, P. Meinecke, E. Passarge, A. Sch

Journal:

Year:

1993

Language:

english

File:

PDF, 1.47 MB

english, 1993