Christina Halgren Harding

Research output

Research output per year 2012 2012 2014 2018

• 4 Journal article
• 1 Ph.D. thesis
• 1 Conference abstract for conference
• 1 Conference abstract in journal

Research output per year

Research output per year

Search results

• 2018

  Risks and Recommendations in Prenatally Detected De Novo Balanced Chromosomal Rearrangements from Assessment of Long-Term Outcomes

  Halgren, C., Nielsen, N. M., Nazaryan-Petersen, L., Silahtaroglu, A., Collins, R. L., Lowther, C., Kjaergaard, S., Frisch, M., Kirchhoff, M., Brøndum-Nielsen, K., Lind-Thomsen, A., Mang, Y., El-Schich, Z., Boring, C. A., Mehrjouy, M. M., Jensen, P. K. A., Fagerberg, C., Krogh, L. N., Hansen, J., Bryndorf, T., & 5 othersHansen, C., Talkowski, M. E., Bak, M., Tommerup, N. & Bache, I., 2018, In: American Journal of Human Genetics. 102, 6, p. 1090-1103 14 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Morbidity 100%
  • Developmental Genes 57%
  • First Pregnancy Trimester 43%
  • Routine Diagnostic Tests 39%
  • Research Design 33%
  15 Citations (Scopus)
• 2017

  NGS mapped breakpoints in balanced chromosomal rearrangements including the first large cohort of healthy carriers

  Tommerup, N., Fonseca, A. C., Mehrjouy, M., Rasmussen, M. B., Bache, I., Halgren, C., Kroisel, P., Midyan, S., Vermeesch, J., Vianna-Morgante, A. M., Abe, K. T., Moretti-Ferreira, D., Paskulin, G., Angelova, L., Rajcan-Separovic, E., Sismani, C., Sedlacek, Z., Fagerberg, C., Brondum-Nielsen, K., Vogel, I., & 36 othersBojesen, A., Ounap, K., Roht, L., Varilo, T., Luukkonen, T., Lespinasse, J., Beneteau, C., Kalscheuer, V. M., Ehmke, N., Daumer-Haas, C., Stefanou, E. G., Marta Czako, Kosztolanyi, G., Sheth, F., Zuffardi, O., Bonaglia, C., Novelli, A., Fannemel, M., Dias, P., Kokalj-Vokac, N., Ramos-Arroyo, M. A., Rodriguez Martinez, L., Guitart, M., Schinzel, A., Engelen, J., Silan, F., Akkari, Y., Batanian, J. R., Kim, H-G., Aristidou, C., De Almeida, C., Lewis, S., Moreno-Igoa, M., Hovhannisyan, A., Jacky, P. & Bak, M., 29 Jun 2017, p. 70. 1 p.

  Research output: Contribution to conference › Conference abstract for conference › Research › peer-review
• 2014

  Neurodevelopmental disorders associated with dosage imbalance of ZBTB20 correlate with the morbidity spectrum of ZBTB20 candidate target genes

  Rasmussen, M. B., Nielsen, J. V., Lourenço, C. M., Melo, J. B., Halgren, C., Geraldi, C. V. L., Marques, W., Rodrigues, G. R., Thomassen, M., Bak, M., Hansen, C., Ferreira, S. I., Venâncio, M., Henriksen, K. F., Lind-Thomsen, A., Carreira, I. M., Jensen, N. A. & Tommerup, N., Sept 2014, In: Journal of Medical Genetics. 51, 9, p. 605-613 9 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Neurodevelopmental Disorders 100%
  • Morbidity 50%
  • Genes 34%
  • Tourette Syndrome 11%
  • Comparative Genomic Hybridization 10%
  23 Citations (Scopus)

• Saturation of the Human Genome with Chromosomal Breakpoints

  Rasmussen, M. B., Schlechter, C. L., Mehrjouy, M. M., Bache, I., Lind-Thomsen, A., Silahtaroglu, A., Kjærgaard, S., Brondum-Nielsen, K., Jensen, P. K. A., Fagerberg, C., Krogh, L. N., Fonseca, A. C. D., Morgante, A. M. V., Abe, K. T., Harding, C. H., Bak, M., Jacky, P. & Tommerup, N., 2014, In: Cytogenetic and Genome Research. 142, 3, 2 p., 2.

  Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
• 2012

  Corpus callosum abnormalities, intellectual disability, speech impairment, and autism in patients with haploinsufficiency of ARID1B

  Hansen, C. H., Kjaergaard, S., Bak, M., Hansen, C., Elschich, Z., Anderson, C. M., Henriksen, K. F., Hjalgrim, H., Kirchhoff, M., Bijlsma, E., Nielsen, M., den Hollander, N., Ruivenkamp, C., Isidor, B., Le Caignec, C., Zannolli, R., Mucciolo, M., Renieri, A., Mari, F., Anderlid, B-M., & 4 othersAndrieux, J., Dieux, A., Tommerup, N. & Bache, I., Sept 2012, In: Clinical Genetics. 82, 3, p. 248-55 8 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Haploinsufficiency 100%
  • Corpus Callosum 87%
  • Autistic Disorder 77%
  • Intellectual Disability 73%
  • Chromosome Breakpoints 20%
  87 Citations (Scopus)

• Haploinsufficiency of CELF4 at 18q12.2 is associated with developmental and behavioral disorders, seizures, eye manifestations, and obesity

  Hansen, C. H., Bache, I., Bak, M., Myatt, M. W., Anderson, C. M., Brøndum-Nielsen, K. & Tommerup, N., Dec 2012, In: European Journal of Human Genetics. 20, 12, p. 1315-1319 5 p.

  Research output: Contribution to journal › Journal article › Research › peer-review

  • Eye Manifestations 100%
  • Haploinsufficiency 98%
  • Epilepsy 64%
  • Obesity 53%
  • Phenotype 46%
  20 Citations (Scopus)

• Neurodevelopmental and Neuropsychiatric Disorders in Carriers of De Novo Balanced Chromosomal Rearrangements

  Hansen, C. H., 30 Mar 2012

  Research output: Book/Report › Ph.D. thesis