E.J. Meijers-Heijboer: search on Z-Library

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1

Identical but not the same: The value of discordant monozygotic twins in genetic research

Petra J.G. Zwijnenburg, Hanne Meijers-Heijboer, Dorret I. Boomsma

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2010

Language:

english

File:

PDF, 219 KB

english, 2010

2

Satisfaction with Prophylactic Mastectomy and Breast Reconstruction in Genetically Predisposed Women

Bresser, Paula J. C., Seynaeve, Caroline, Gool, Arthur R. Van, Brekelmans, Cecile T., Meijers-Heijboer, Hanne, van Geel, Albert N., Menke-Pluijmers, Marian B., Duivenvoorden, Hugo J., Klijn, Jan G. M.

Journal:

Plastic & Reconstructive Surgery

Year:

2006

Language:

english

File:

PDF, 170 KB

english, 2006

3

Preconception carrier screening for multiple disorders: evaluation of a screening offer in a Dutch founder population

Mathijssen, Inge B., Holtkamp, Kim C. A., Ottenheim, Cecile P. E., van Eeten-Nijman, Janneke M. C., Lakeman, Phillis, Meijers-Heijboer, Hanne, van Maarle, Merel C., Henneman, Lidewij

Journal:

European Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 541 KB

english, 2018

4

The association between cancer family history and ovarian cancer risk in BRCA1/2 mutation carriers: can it be explained by the mutation position?

Teixeira, Natalia, van der Hout, Annemieke, Oosterwijk, Jan C., Vos, Janet R., Devilee, Peter, van Engelen, Klaartje, Meijers-Heijboer, Hanne, van der Luijt, Rob B., Kriege, Mieke, Mensenkamp, Arjen R

Journal:

European Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 704 KB

english, 2018

5

Tumour characteristics, survival and prognostic factors of hereditary breast cancer from BRCA2-, BRCA1- and non-BRCA1/2 families as compared to sporadic breast cancer cases

C.T.M. Brekelmans, M.M.A. Tilanus-Linthorst, C. Seynaeve, A. vd Ouweland, M.B.E. Menke-Pluymers, C.C.M. Bartels, M. Kriege, A.N. van Geel, C.W. Burger, A.M.M. Eggermont, H. Meijers-Heijboer, J.G.M. Kl

Journal:

European Journal of Cancer

Year:

2007

Language:

english

File:

PDF, 214 KB

english, 2007

6

Psychological impact of receiving a BRCA1/BRCA2 test result

Litanja Lodder, Petra G. Frets, R. Willem Trijsburg, E. Johanna Meijers-Heijboer, Jan G.M. Klijn, Hugo J. Duivenvoorden, Aad Tibben, Anja Wagner, Conny A. van der Meer, Ans M.W. van den Ouweland, Mart

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 164 KB

english, 2001

7

The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study

Iris van Oostrom, Hanne Meijers-Heijboer, Hugo J. Duivenvoorden, Annette H. J. T. Bröcker-Vriends, Christi J. van Asperen, Rolf H. Sijmons, Caroline Seynaeve, Arthur R. Van Gool, Jan G. M. Klijn, Aad

Journal:

Psycho-Oncology

Year:

2007

Language:

english

File:

PDF, 154 KB

english, 2007

8

Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

Brohet, R. M., Velthuizen, M. E., Hogervorst, F. B. L., EJ Meijers-Heijboer, H., Seynaeve, C., Collee, M. J., Verhoef, S., Ausems, M. G. E. M., Hoogerbrugge, N., van Asperen, C. J., Gomez Garcia, E.,

Journal:

Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 1.00 MB

english, 2014

9

Whole-genome sequencing in health care

van El, Carla G, Cornel, Martina C, Borry, Pascal, Hastings, Ros J, Fellmann, Florence, Hodgson, Shirley V, Howard, Heidi C, Cambon-Thomsen, Anne, Knoppers, Bartha M, Meijers-Heijboer, Hanne, Scheffer

Journal:

European Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 248 KB

english, 2013

10

Rapid detection of BRCA1 mutations by the protein truncation test

Hogervorst, Frans B.L., Cornelis, Renée S., Bout, Mattie, Vliet, Margreethe van, Oosterwijk, Jan C., Olmer, Renske, Bakker, Bert, Klijn, Jan G.M., Vasen, Hans F.A., Meijers-Heijboer, Hanna

Journal:

Nature Genetics

Year:

1995

File:

PDF, 638 KB

1995

11

Ipsilateral breast tumour recurrence in hereditary breast cancer following breast-conserving therapy

C Seynaeve, L.C Verhoog, L.M.C van de Bosch, A.N van Geel, M Menke-Pluymers, E.J Meijers-Heijboer, A.M.W van den Ouweland, A Wagner, C.L Creutzberg, M.F Niermeijer, J.G.M Klijn, C.T.M Brekelmans

Journal:

European Journal of Cancer

Year:

2004

Language:

english

File:

PDF, 240 KB

english, 2004

12

IVF and retinoblastoma revisited

Charlotte J. Dommering, Annemarie H. van der Hout, Hanne Meijers-Heijboer, Tamara Marees, Annette C. Moll

Journal:

Fertility and Sterility

Year:

2012

Language:

english

File:

PDF, 71 KB

english, 2012

13

Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 Gene

Anja Wagner, Alicia Barrows, Juul Th. Wijnen, Heleen van der Klift, Patrick F. Franken, Paul Verkuijlen, Hidewaki Nakagawa, Marjan Geugien, Shantie Jaghmohan-Changur, Cor Breukel, Hanne Meijers-Heijbo

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 303 KB

english, 2003

14

Training genetic counselors — what should this entail?

H. Meijers-Heijboer

Journal:

European Journal of Cancer Supplements

Year:

2006

Language:

english

File:

PDF, 113 KB

english, 2006

15

Complete COL1A1 allele deletions in osteogenesis imperfecta

van Dijk, Fleur S, Huizer, Margriet, Kariminejad, Ariana, Marcelis, Carlo L, Plomp, Astrid S, Terhal, Paulien A, Meijers-Heijboer, Hanne, Weiss, Marjan M, van Rijn, Rick R, Cobben, Jan M, Pals, Gerard

Journal:

Genetics in Medicine

Year:

2010

Language:

english

File:

PDF, 660 KB

english, 2010

16

Reproductive decision-making: a qualitative study among couples at increased risk of having a child with retinoblastoma

CJ Dommering, MR Van Den Heuvel, AC Moll, SM Imhof, H Meijers-Heijboer, L Henneman

Journal:

Clinical Genetics

Year:

2010

Language:

english

File:

PDF, 540 KB

english, 2010

17

Targeted carrier screening for four recessive disorders: High detection rate within a founder population

Mathijssen, Inge B., Henneman, Lidewij, van Eeten-Nijman, Janneke M.C., Lakeman, Phillis, Ottenheim, Cecile P.E., Redeker, Egbert J.W., Ottenhof, Winnie, Meijers-Heijboer, Hanne, van Maarle, Merel C.

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 404 KB

english, 2015

18

A Dutch Fanconi Anemia FANCC Founder Mutation in Canadian Manitoba Mennonites

de Vries, Yne, Lwiwski, Nikki, Levitus, Marieke, Kuyt, Bertus, Israels, Sara J., Arwert, Fré, Zwaan, Michel, Greenberg, Cheryl R., Alter, Blanche P., Joenje, Hans, Meijers-Heijboer, Hanne

Journal:

Year:

2012

Language:

english

File:

PDF, 749 KB

english, 2012

19

A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships

Iris van Oostrom, Hanne Meijers-Heijboer, Hugo J. Duivenvoorden, Annette H. J. T. Bröcker-Vriends, Christi J. van Asperen, Rolf H. Sijmons, Caroline Seynaeve, Arthur R. Van Gool, Jan G. M. Klijn, Sama

Journal:

Psycho-Oncology

Year:

2007

Language:

english

File:

PDF, 170 KB

english, 2007

20

10.1038/13773

Wijnen, Juul, Leeuw, Wiljo de, Vasen, Hans, Klift, Heleen van der, Møller, Pål, Stormorken, Astrid, Meijers-Heijboer, Hanne, Lindhout, Dick, Menko, Fred, Vossen, Sandra, Möslein, Gabriela, Tops, Carli

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 171 KB

english, 1999

21

Variants in CHEK2 Other than 1100delC Do Not Make a Major Contribution to Breast Cancer Susceptibility

Mieke Schutte, Sheila Seal, Rita Barfoot, Hanne Meijers-Heijboer, Marijke Wasielewski, D. Gareth Evans, Diana Eccles, Carel Meijers, Frans Lohman, Jan Klijn, Ans van den Ouweland, P. Andrew Futreal, K

Journal:

The American Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 410 KB

english, 2003

22

Effect on a Dutch family of predictive DNA-testing for hereditary breast and ovarian cancer

A.C. Dudok de Wit, E.J. Meijers-Heijboer, A. Tibben, P.G. Frets, J.G.M. Klijn, P. Devilee, M.F. Niermeijer

Journal:

Year:

1994

Language:

english

File:

PDF, 161 KB

english, 1994

23

A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression

Kooi, Irsan E., Mol, Berber M., Massink, Maarten P. G., de Jong, Marcus C., de Graaf, Pim, van der Valk, Paul, Meijers-Heijboer, Hanne, Kaspers, Gertjan J. L., Moll, Annette C., te Riele, Hein, Cloos,

Journal:

Year:

2016

Language:

english

File:

PDF, 3.04 MB

english, 2016

24

Genetic susceptibility for breast cancer: How many more genes to be found?

R.A. Oldenburg, H. Meijers-Heijboer, C.J. Cornelisse, P. Devilee

Journal:

Critical Reviews in Oncology/Hematology

Year:

2007

Language:

english

File:

PDF, 1.29 MB

english, 2007

25

RB1mutations and second primary malignancies after hereditary retinoblastoma

Charlotte J. Dommering, Tamara Marees, Annemarie H. van der Hout, Saskia M. Imhof, Hanne Meijers-Heijboer, Peter J. Ringens, Flora E. van Leeuwen, Annette C. Moll

Journal:

Familial Cancer

Year:

2012

Language:

english

File:

PDF, 281 KB

english, 2012

26

PP-4-40 Histologic findings in prophylactic mastectomy specimens from women with hereditary risk factors

L.C. Verhoog, A.N. van Geel, S.C. Henzen-Logmans, C. Seynaeve, M. Tilanus-Linthorst, C.C.M. Bartels, M. Meijers-Heijboer, P. Devilee, J.G.M. Klijn

Journal:

European Journal of Cancer

Year:

1996

Language:

english

File:

PDF, 168 KB

english, 1996

27

Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome

Beunders, Gea, de Munnik, Sonja A, Van der Aa, Nathalie, Ceulemans, Berten, Voorhoeve, Els, Groffen, Alexander J, Nillesen, Willy M, Meijers-Heijboer, Elizabeth J, Frank Kooy, R, Yntema, Helger G, Sis

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.11 MB

english, 2015

28

Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan Syndrome

Franken, R., den Hartog, A. W., Radonic, T., Micha, D., Maugeri, A., van Dijk, F. S., Meijers-Heijboer, H. E., Timmermans, J., Scholte, A. J., van den Berg, M. P., Groenink, M., Mulder, B. J. M., Zwin

Journal:

Circulation Cardiovascular Genetics

Year:

2015

Language:

english

File:

PDF, 1.52 MB

english, 2015

29

Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers

Heemskerk-Gerritsen, Bernadette A. M., Jager, Agnes, Koppert, Linetta B., Obdeijn, A. Inge-Marie, Collée, Margriet, Meijers-Heijboer, Hanne E. J., Jenner, Denise J., Oldenburg, Hester S. A., van Engel

Journal:

Breast Cancer Research and Treatment

Year:

2019

Language:

english

File:

PDF, 960 KB

english, 2019

30

Low-penetrance susceptibility to breast cancer due to CHEK2*1100delC in noncarriers of BRCA1 or BRCA2 mutations

Meijers-Heijboer, Hanne, van den Ouweland, Ans, Klijn, Jan, Wasielewski, Marijke, de Snoo, Anja, Oldenburg, Rogier, Hollestelle, Antoinette, Houben, Mark, Crepin, Ellen, van Veghel-Plandsoen, Monique

Journal:

Nature Genetics

Year:

2002

Language:

english

File:

PDF, 109 KB

english, 2002

31

Gene screening and prevention of hereditary breast cancer: a clinical view

J.G.M Klijn, H Meijers-Heijboer

Journal:

European Journal of Cancer Supplements

Year:

2003

Language:

english

File:

PDF, 311 KB

english, 2003

32

Long-term registration of prophylactic mastectomy (PM) in BRCA1/2 mutation carriers and women at increased breast cancer (BC) risk due to a family history at a single institution

B.A.M. Heemskerk-Gerritsen, Menke-Pluymers, C. Seynaeve, M.M.A. Tilanus-Linthorst, C.C.M. Bartels, E.J. Meijers-Heijboer, J.G.M. Klijn, A.N. van Geel, C.T.M. Brekelmans

Journal:

European Journal of Cancer Supplements

Year:

2006

Language:

english

File:

PDF, 131 KB

english, 2006

33

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

Wiljo J. F. de Leeuw, JanWillem Dierssen, Hans F. A. Vasen, Juul Th. Wijnen, Gemma G. Kenter, Hanne Meijers-Heijboer, Annette Brocker-Vriends, Astrid Stormorken, Pal Moller, Fred Menko, Cees J. Cornel

Journal:

The Journal of Pathology

Year:

2000

Language:

english

File:

PDF, 309 KB

english, 2000

34

Spondyloepiphyseal dysplasia, Omani type: Further definition of the phenotype

Mirjam H.H. van Roij, Shuji Mizumoto, Shuhei Yamada, Tim Morgan, M.B. Tan-Sindhunata, H. Meijers-Heijboer, J.I.L.M. Verbeke, David Markie, Kazuyuki Sugahara, Stephen P. Robertson

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 193 KB

english, 2008

35

A BRCA1/2 mutation, high breast density and prominent pushing margins of a tumor independently contribute to a frequent false-negative mammography

Madeleine Tilanus-Linthorst, Leon Verhoog, Inge-Marie Obdeijn, Karina Bartels, Marian Menke-Pluymers, Alexander Eggermont, Jan Klijn, Hanne Meijers-Heijboer, Theo van der Kwast, Cecile Brekelmans

Journal:

International Journal of Cancer

Year:

2002

Language:

english

File:

PDF, 679 KB

english, 2002

36

TwoTP53germline mutations in a classical Li-Fraumeni syndrome family

Liselotte P. van Hest, Mariëlle W. G. Ruijs, Anja Wagner, Conny A. van der Meer, Senno Verhoef, Laura J. van‘t Veer, Hanne Meijers-Heijboer

Journal:

Familial Cancer

Year:

2007

Language:

english

File:

PDF, 155 KB

english, 2007

37

LONG-TERM FOLLOW-UP OF PATIENTS WITH RETINITIS PIGMENTOSA TYPE 12 CAUSED BY CRB1 MUTATIONS

Mathijssen, Inge B., Florijn, Ralph J., van den Born, L. Ingeborgh, Zekveld-Vroon, Renate C., ten Brink, Jacoline B., Plomp, Astrid S., Baas, Frank, Meijers-Heijboer, Hanne, Bergen, Arthur A. B., van

Journal:

Year:

2017

Language:

english

File:

PDF, 887 KB

english, 2017

38

Breast Cancer Screening in High-Risk Women

Brekelmans, C. T. M., Bartels, C. C. M., Crepin, E., van Geel, A. N., Meijers-Heijboer, H., Seynaeve, C., Tilanus-Linthorst, M. M. A., Verhoog, L. C., Wagner, A., Klijn, J. G. M.

Journal:

Disease Markers

Year:

1999

Language:

english

File:

PDF, 1.09 MB

english, 1999

39

Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era

Stuurman, Kyra E, Joosten, Marieke, van der Burgt, Ineke, Elting, Mariet, Yntema, Helger G, Meijers-Heijboer, Hanne, Rinne, Tuula

Journal:

Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 444 KB

english, 2019

40

Biallelic germline mutations of mismatch-repair genes : A possible cause for multiple pediatric malignancies

Jan-Werner Poley, Anja Wagner, Monique M. C. P. Hoogmans, Fred H. Menko, Carli Tops, Johan M. Kros, Roel E. Reddingius, Hanne Meijers-Heijboer, Ernst J. Kuipers, Winand N. M. Dinjens, on behalf of the

Journal:

Year:

2007

Language:

english

File:

PDF, 1.19 MB

english, 2007

41

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study

I Van Oostrom, H Meijers-Heijboer, HJ Duivenvoorden, AHJT Bröcker-Vriends, CJ Van Asperen, RH Sijmons, C Seynaeve, AR Van Gool, JGM Klijn, A Tibben

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 136 KB

english, 2007

42

Mutation frequency ofPRKAR1Band the major familial dementia genes in a Dutch early onset dementia cohort

Cohn-Hokke, P. E., Wong, T. H., Rizzu, P., Breedveld, G., van der Flier, W. M., Scheltens, P., Baas, F., Heutink, P., Meijers-Heijboer, E. J., van Swieten, J. C., Pijnenburg, Y. A. L.

Journal:

Journal of Neurology

Year:

2014

Language:

english

File:

PDF, 222 KB

english, 2014

43

‘A Low Risk Is Still a Risk’: Exploring Women’s Attitudes towards Genetic Testing for Breast Cancer Susceptibility in Order to Target Disease Prevention

Henneman, L., Timmermans, D.R., Bouwman, C.M., Cornel, M.C., Meijers-Heijboer, H.

Journal:

Public Health Genomics

Year:

2011

Language:

english

File:

PDF, 167 KB

english, 2011

44

Genomic landscape of retinoblastoma in Rb -/- p130 -/- mice resembles human retinoblastoma

Kooi, Irsan E., van Mil, Saskia E., MacPherson, David, Mol, Berber M., Moll, Annette C., Meijers-Heijboer, Hanne, Kaspers, Gertjan J.L., Cloos, Jacqueline, te Riele, Hein, Dorsman, Josephine C.

Journal:

Genes, Chromosomes and Cancer

Year:

2016

Language:

english

File:

PDF, 2.65 MB

english, 2016

45

Effectiveness of Breast Cancer Surveillance in BRCA1/2 Gene Mutation Carriers and Women With High Familial Risk

Brekelmans, C.T.M., Seynaeve, C., Bartels, C.C.M., Tilanus-Linthorst, M.M.A., Meijers-Heijboer, E.J., Crepin, C.M.G., van Geel, A.N., Menke, M., Verhoog, L.C., van den Ouweland, A., Obdeijn, I.M., Kli

Journal:

Journal of Clinical Oncology

Year:

2001

Language:

english

File:

PDF, 56 KB

english, 2001

46

With expanded carrier screening, founder populations run the risk of being overlooked

Mathijssen, Inge B., van Maarle, Merel C., Kleiss, Iris I.M., Redeker, Egbert J.W., ten Kate, Leo P., Henneman, Lidewij, Meijers-Heijboer, Hanne

Journal:

Journal of Community Genetics

Year:

2017

Language:

english

File:

PDF, 287 KB

english, 2017

47

Males at–risk for the BRCA1-1ene, the psychological impact

A. C. Dudok de Wit, A. Tibben, P. G. Frets, E. J. Meijers-Heijboer, P. Devilee, M. F. Niermeijer

Journal:

Psycho-Oncology

Year:

1996

Language:

english

File:

PDF, 566 KB

english, 1996

48

Deletions at chromosome regions 7q11.23 and 7q36 in a patient with Williams syndrome

Cokkie H. Wouters, Hanne J. Meijers-Heijboer, Bert J.F.M.M. Eussen, Annette A. van der Heide, Rob B. van Luijk, Ellen van Drunen, Berna B. Beverloo, Frank Visscher, Jan O. Van Hemel

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 250 KB

english, 2001

49

Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era

Stuurman, Kyra E, Joosten, Marieke, van der Burgt, Ineke, Elting, Mariet, Yntema, Helger G, Meijers-Heijboer, Hanne, Rinne, Tuula

Journal:

Journal of Medical Genetics

Year:

2019

File:

PDF, 444 KB

2019

50

Long Term Follow-up of HNPCC Gene Mutation Carriers: Compliance with Screening and Satisfaction with Counseling and Screening Procedures

Anja Wagner, Ingrid van Kessel, Mieke G. Kriege, Carli M. J. Tops, Juul Th. Wijnen, Hans F. A. Vasen, Conny A. van der Meer, Iris I. H. van Oostrom, Hanne Meijers-Heijboer

Journal:

Familial Cancer

Year:

2005

Language:

english

File:

PDF, 169 KB

english, 2005

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