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1

A diode-pumped continuous-wave Yb:KGW laser with Ng-axis polarized output

A. Major, D. Sandkuijl, V. Barzda

Journal:

Laser Physics Letters

Year:

2009

Language:

english

File:

PDF, 72 KB

english, 2009

2

Femtosecond Yb:KGd(WO4)2 laser with > 100 nJ of pulse energy

A. Major, R. Cisek, D. Sandkuijl, V. Barzda

Journal:

Laser Physics Letters

Year:

2009

Language:

english

File:

PDF, 82 KB

english, 2009

3

Facioscapulohumeral muscular dystrophy in the dutch population

Dr. G. W. Padberg, Dr. R. R. Frants, O. F. Brouwer, C. Wijmenga, E. Bakker, L. A. Sandkuijl

Journal:

Year:

1995

Language:

english

File:

PDF, 404 KB

english, 1995

4

Perspectives of identity by descent (IBD) mapping in founder populations

G. J. TE MEERMAN, M. A. VAN DER MEULEN, L. A. SANDKUIJL

Journal:

Clinical & Experimental Allergy

Year:

1995

Language:

english

File:

PDF, 2.66 MB

english, 1995

5

10.1038/90038

Njajou, Omer T., Vaessen, Norbert, Joosse, Marijke, Berghuis, Bianca, van Dongen, Jeroen W.F., Breuning, Martijn H., Snijders, Pieter J.L.M., Rutten, Wim P.F., Sandkuijl, Lodewijk A., Oostra, Ben A.,

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 1.07 MB

english, 2001

6

Cost-Effective Designs for Linkage Disequilibrium Mapping of Complex Traits

Susan K. Service, Lodewijk A. Sandkuijl, Nelson B. Freimer

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 1.15 MB

english, 2003

7

Use of linkage disequilibrium approaches to map genes for bipolar disorder in the Costa Rican population

Escamilla, Michael A., Spesny, Mitzi, Reus, Victor I., Gallegos, Alvaro, Meza, Luis, Molina, Julio, Sandkuijl, Lodewijk A., Fournier, Eduardo, Leon, Pedro E., Smith, Lauren B., Freimer, Nelson B.

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 1.20 MB

1996

8

An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees

Freimer, N. B., Reus, V. I., Escamilla, M., Spesny, M., Smith, L., Service, S., Gallegos, A., Meza, L., Batki, S., Vinogradov, S., Leon, P., Sandkuijl, L. A.

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 1.02 MB

1996

9

Linkage analysis of bipolar illness with X-chromosome DNA markers: A susceptibility gene in Xq27-q28 cannot be excluded

A. De Bruyn, P. Raeymaekers, K. Mendelbaum, L. A. Sandkuijl, G. Raes, V. Delvenne, D. Hirsch, L. Staner, J. Mendlewicz, Dr. C. Van Broeckhoven

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 821 KB

english, 1994

10

Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis

Tom J. de Koning, Lodewijk A. Sandkuijl, Jan E. A. R. de Schryver, Eric A. M. Hennekam, Frits A. Beemer, Dr. Roderick H. J. Houwen

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 404 KB

english, 1995

11

Genetic mapping using haplotype and model-free linkage analysis supports previous evidence for a locus predisposing to severe bipolar disorder at 5q31-33

Kyung Sue Hong, L. Alison McInnes, Susan K. Service, Terry Song, Jennifer Lucas, Sandra Silva, Eduardo Fournier, Pedro León, Julio Molina, Victor I. Reus, Lodewijk A. Sandkuijl, Nelson B. Freimer

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 143 KB

english, 2004

12

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

Kaate R. J. Vanmolkot, Esther E. Kors, Jouke-Jan Hottenga, Gisela M. Terwindt, Joost Haan, Wil A. J. Hoefnagels, David F. Black, Lodewijk A. Sandkuijl, Rune R. Frants, Michel D. Ferrari, Arn M. J. M.

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 409 KB

english, 2003

13

Score test for detecting linkage to quantitative traits

H. Putter, L.A. Sandkuijl, J.C. van Houwelingen

Journal:

Genetic Epidemiology

Year:

2002

Language:

english

File:

PDF, 119 KB

english, 2002

14

Maximum-likelihood estimation in linkage heterogeneity models including additional information via the EM algorithm

Jeanine J. Houwing-Duistermaat, Lodewijk A. Sandkuijl, Arthur A. B. Bergen, Hans C. van Houwelingen

Journal:

Genetic Epidemiology

Year:

1995

Language:

english

File:

PDF, 743 KB

english, 1995

15

Exclusion of candidate gene loci for adult onset primary open-angle glaucoma in a genetically isolated population

Caa Hulsman, Jjm Willemse-Assink, Ptvm De Jong, M Lettink, La Sandkuijl, Aab Bergen

Journal:

Clinical Genetics

Year:

2002

Language:

english

File:

PDF, 87 KB

english, 2002

16

Familial Partial Epilepsy with Variable Foci in a Dutch Family: Clinical Characteristics and Confirmation of Linkage to Chromosome 22q

Petra M. C. Callenbach, Arn M. J. M. Van Den Maagdenberg, Jouke J. Hottenga, Eelke H. Van Den Boogerd, René F. M. De Coo, Dick Lindhout, Rune R. Frants, Lodewijk A. Sandkuijl, Oebele F. Brouwer

Journal:

Year:

2003

Language:

english

File:

PDF, 109 KB

english, 2003

17

Linkage analysis of factor VIII and von Willebrand factor loci as quantitative trait loci

M. C. H. De Visser, L. A. Sandkuijl, R. P. M. Lensen, H. L. Vos, F. R. Rosendaal, R. M. Bertina

Journal:

Journal of Thrombosis and Haemostasis

Year:

2003

Language:

english

File:

PDF, 88 KB

english, 2003

18

Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

Arne May, Roel A. Ophoff, Gisela M. Terwindt, Christine Urban, Ronald Eijk, Joost Haan, H. Christoph Diener, Dick Lindhout, Rune R. Frants, Lodewijk A. Sandkuijl, Michel D. Ferrari

Journal:

Year:

1995

Language:

english

File:

PDF, 413 KB

english, 1995

19

Refined localization of TSC1 by combined analysis of 9q34 and 16pl3 data in 14 tuberous sclerosis families

Bart Janssen, Julian Sampson, Mieke Est, Wout Deelen, Senno Verhoef, Ian Daniels, Arjenne Hesseling, Phillip Brook-Carter, Mark Nellist, Dick Lindhout, Lodewijk Sandkuijl, Dicky Halley

Journal:

Year:

1994

Language:

english

File:

PDF, 336 KB

english, 1994

20

Pure hereditary spastic paraparesis: an exclusion map covering more than 40% of the autosomal genome

Judith C. T. Deutekom, Richard P. M. Bruyn, Nicolle Boom, Lodewijk A. Sandkuijl, George W. Padberg, Rune R. Frants

Journal:

Year:

1994

Language:

english

File:

PDF, 537 KB

english, 1994

21

Polymerisation and crosslinking of fibrin monomers in diabetes mellitus

A. Lütjens, T. W. Jonkhoff-Slok, C. Sandkuijl, E. A. v. d. Veen, J. v. d. Meer

Journal:

Year:

1988

Language:

english

File:

PDF, 906 KB

english, 1988

22

Molecular genetic analysis of two families with keratosis follicularis spinulosa decalvans: refinement of gene localization and evidence for genetic heterogeneity

J. C. Oosterwijk, Gabriela Richard, Michiel J. R. van der Wielen, E. van de Vosse, Wolfgang Harth, Lodewijk A. Sandkuijl, Egbert Bakker, Gert-Jan B. van Ommen

Journal:

Year:

1997

Language:

english

File:

PDF, 68 KB

english, 1997

23

Genome-wide screen in obese pedigrees with type 2 diabetes mellitus from a defined Dutch population

J. H. Van Tilburg, L. A. Sandkuijl, L. Franke, E. Strengman, P. L. Pearson, T. W. Van Haeften, C. Wijmenga

Journal:

European Journal of Clinical Investigation

Year:

2003

Language:

english

File:

PDF, 244 KB

english, 2003

24

Partial Cosegregation of Familial Hemiplegic Migraine and a Benign Familial Infantile Epileptic Syndrome

G. M. Terwindt, R. A. Ophoff, D. Lindhout, J. Haan, D. J. J. Halley, L. A. Sandkuijl, O. F. Brouwer, R. R. Frants, M. D. Ferrari

Journal:

Year:

1997

Language:

english

File:

PDF, 642 KB

english, 1997

25

Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families

de Snoo, Femke A, Hottenga, Jouke-Jan, Gillanders, Elizabeth M, Sandkuijl, Loudewijk A, Jones, Mary Pat, Bergman, Wilma, van der Drift, Clasine, van Leeuwen, Inge, van Mourik, Lenny, Huurne, Jeanet A

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 172 KB

english, 2008

26

Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families

de Snoo, Femke A, Hottenga, Jouke-Jan, Gillanders, Elizabeth M, Sandkuijl, Lodewijk A, Jones, Mary Pat, Bergman, Wilma, van der Drift, Clasine, van Leeuwen, Inge, van Mourik, Leny, Huurne, Jeanet A C

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 33 KB

english, 2008

27

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q

Heutink, Peter, Zguricas, Julia, Oosterhout, Linda van, Breedveld, Guido J., Testers, Leon, Sandkuijl, Lodewijk A., Snijders, Pieter J.L.M., Weissenbach, Jean, Lindhout, Dick, Hovius, Steven E.R

Journal:

Nature Genetics

Year:

1994

File:

PDF, 504 KB

1994

28

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds

Gruis, Nelleke A., van der Velden, Pieter A., Sandkuijl, Lodewijk A., Prins, Duncan E., Weaver-Feldhaus, Jane, Kamb, Alexander, Bergman, Wilma, Frants, Rune R.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 310 KB

1995

29

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

van den Ouweland, J.M.W., Lemkes, H.H.P.J., Ruitenbeek, W., Sandkuijl, L.A., de Vijlder, M.F., Struyvenberg, P.A.A., van de Kamp, J.J.P., Maassen, J.A.

Journal:

Nature Genetics

Year:

1992

File:

PDF, 562 KB

1992

30

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

Wijmenga, Cisca, Hewitt, Jane E., Sandkuijl, Lodewijk A., Clark, Lorraine N., Wright, Tracy J., Dauwerse, Hans G., Gruter, Anne-Marie, Hofker, Marten H., Moerer, Petra, Williamson, Robert

Journal:

Nature Genetics

Year:

1992

File:

PDF, 644 KB

1992

31

Schizophrenia susceptibility and chromosome 6p24–22

Lennon, David P., Sandkuijl, Lodewijk A., Crowe, Raymond R., Silverman, Jeremy M., Mohs, Richard C., Siever, Larry J., Endicott, Jean, Sharpe, Lawrence, Mowry, Bryan J., Nancarrow, Derek J.

Journal:

Nature Genetics

Year:

1995

File:

PDF, 375 KB

1995

32

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

van Overveld, Petra G M, Lemmers, Richard J F L, Sandkuijl, Lodewijk A, Enthoven, Leo, Winokur, Sara T, Bakels, Floor, Padberg, George W, van Ommen, Gert-Jan B, Frants, Rune R, van der Maarel, Silvère

Journal:

Nature Genetics

Year:

2003

Language:

english

File:

PDF, 200 KB

english, 2003

33

Chromosome 4 localization of a second gene for autosomal dominant polycystic kidney disease

Peters, D.J.M., Spruit, L., Saris, J.J., Ravine, D., Sandkuijl, L.A., Fossdal, R., Boersma, J., van Eijk, R., Nørby, S., Constantinou-Deltas, C.D.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 388 KB

1993

34

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

Houwen, Roderick H. J., Baharloo, Siamak, Blankenship, Kathleen, Raeymaekers, Peter, Juyn, Jenneke, Sandkuijl, Lodewijk A., Freimer, Nelson B.

Journal:

Nature Genetics

Year:

1994

File:

PDF, 1.28 MB

1994

35

Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere

Lemmers, Richard J.L.F., de Kievit, Peggy, Sandkuijl, Lodewijk, Padberg, George W., van Ommen, Gert-Jan B., Frants, Rune R., van der Maarel, Silvère M.

Journal:

Nature Genetics

Year:

2002

Language:

english

File:

PDF, 130 KB

english, 2002

36

Variance-Component Analysis of Obesity in Type 2 Diabetes Confirms Loci on Chromosomes 1q and 11q

Jonathan H.O. van Tilburg, Lodewijk A. Sandkuijl, Eric Strengman, Peter L. Pearson, Timon W. van Haeften, Cisca Wijmenga

Journal:

Year:

2003

Language:

english

File:

PDF, 52 KB

english, 2003

37

Endemic Tyrolean infantile cirrhosis is not an allelic variant of Wilson's disease

Wijmenga, C, Müller, T, Murli, I S, Brunt, T, Feichtinger, H, Schönitzer, D, Houwen, R H J, Müller, W, Sandkuijl, L A, Pearson, P L

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 74 KB

english, 1999

38

Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies

Terwindt, G M, Ophoff, R A, Haan, Joost, Sandkuijl, L A, Frants, R R

Journal:

European Journal of Human Genetics

Year:

1998

Language:

english

File:

PDF, 178 KB

english, 1998

39

Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling

Ausems, M G E M, Verbiest, J, Hermans, M M P, Kroos, M A, Beemer, F A, Wokke, J H J, Sandkuijl, L A, Reuser, A J J, van der Ploeg, A T

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 176 KB

english, 1999

40

X-linked recessive inheritance of radial ray deficiencies in a family with four affected males

Galjaard, Robert-Jan H, Kostakoglu, Naci, Hoogeboom, Jeannette J M, Breedveld, Guido J, van der Linde, Herma C, Hovius, Steven ER, Oostra, Ben A, Sandkuijl, Lodewijk A, Akarsu, A Nurten, Heutink, Pete

Journal:

European Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 150 KB

english, 2001

41

Candidate gene approach in association studies: would the factor V Leiden mutation have been found by this approach?

van Hylckama Vlieg, Astrid, Sandkuijl, Lodewijk A, Rosendaal, Frits R, Bertina, Rogier M, Vos, Hans L

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

42

Linkage disequilibrium in young genetically isolated Dutch population

Aulchenko, Yurii S, Heutink, Peter, Mackay, Ian, Bertoli-Avella, Aida M, Pullen, Jan, Vaessen, Norbert, Rademaker, Tessa AM, Sandkuijl, Lodewijk A, Cardon, Lon, Oostra, Ben

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 138 KB

english, 2004

43

Defining the contribution of the HLA region to cis DQ2-positive coeliac disease patients

van Belzen, M J, Koeleman, B P C, Crusius, J B A, Meijer, J W R, Bardoel, A F J, Pearson, P L, Sandkuijl, L A, Houwen, R H J, Wijmenga, C

Journal:

Genes and Immunity

Year:

2004

Language:

english

File:

PDF, 109 KB

english, 2004

44

Association between an agouti-related protein gene polymorphism and anorexia nervosa

Vink, T, Hinney, A, van Elburg, A A, van Goozen, S H M, Sandkuijl, L A, Sinke, R J, Herpertz-Dahlmann, B-M, Hebebrand, J, Remschmidt, H, van Engeland, H

Journal:

Molecular Psychiatry

Year:

2001

Language:

english

File:

PDF, 174 KB

english, 2001

45

034 Chromosomal location of vanishing white matter

P.A.J. Leegwater, L.A. Sandkuijl, S. Naidu, J.C. Pronk, M.S. Van Der Knaap

Journal:

European Journal of Paediatric Neurology

Year:

1999

Language:

english

File:

PDF, 144 KB

english, 1999

46

Differential microscopy for fluorescence-detected nonlinear absorption linear anisotropy based on a staggered two-beam femtosecond Yb:KGW oscillator

Sandkuijl, Daaf, Cisek, Richard, Major, Arkady, Barzda, Virginijus

Journal:

Biomedical Optics Express

Year:

2010

Language:

english

File:

PDF, 1.99 MB

english, 2010

47

Efficient frequency doubling of a femtosecond Yb:KGW laser in a BiB_3O_6 crystal

Major, Arkady, Sandkuijl, Daaf, Barzda, Virginijus

Journal:

Year:

2009

Language:

english

File:

PDF, 82 KB

english, 2009

48

Dominant Hemochromatosis Due to N144H Mutation of SLC11A3: Clinical and Biological Characteristics

Omer T. Njajou, Gerard de Jong, Bianca Berghuis, Norbert Vaessen, Pieter J.L.M. Snijders, Jan P. Goossens, John H.P. Wilson, Martijn H. Breuning, Ben A. Oostra, Peter Heutink, Lodewijk A. Sandkuijl, C

Journal:

Blood Cells, Molecules, and Diseases

Year:

2002

Language:

english

File:

PDF, 34 KB

english, 2002

49

Genetic Heterogeneity of Familial Hemiplegic Migraine

Roel A. Ophoff, Ronald van Eijk, Lodewijk A. Sandkuijl, Gisela M. Terwindt, Caroline P.M. Grubben, Joost Haan, Dick Lindhout, Michel D. Ferrari, Rune R. Frants

Journal:

Year:

1994

File:

PDF, 322 KB

1994

50

Assignment of a Gene for Autosomal Recessive Retinitis Pigmentosa (RP12) to Chromosome 1q31-q32.1 in an Inbred and Genetically Heterogeneous Disease Population

Simone van Soest, L.Ingeborgh van den Born, Andreas Gal, G.Jane Farrar, Liesbeth M. Bleeker-Wagemakers, Andries Westerveld, Peter Humphries, Lodewijk A. Sandkuijl, Arthur A.B. Bergen

Journal:

Year:

1994

File:

PDF, 545 KB

1994