Harvard Catalyst Profiles

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Louise Edith Wilkins-Haug, M.D., Ph.D.

Co-Author

This page shows the publications co-authored by Louise Wilkins-Haug and Rosemary Reiss.
Connection Strength

1.947
  1. Reiss RE, Discenza M, Foster J, Dobson L, Wilkins-Haug L. Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous? Prenat Diagn. 2017 May; 37(5):515-520.
    View in: PubMed
    Score: 0.785
  2. Reiss R, Ahern D, Sandstrom M, Wilkins-Haug L. Recurrent enlarged nuchal translucency: first trimester presentation of a familial 15q26?qter deletion. . 2015 Mar; 167A(3):612-6.
    View in: PubMed
    Score: 0.676
  3. Bunnell ME, Wilkins-Haug L, Reiss R. Should embryos with autosomal monosomy by preimplantation genetic testing for aneuploidy be transferred?: Implications for embryo selection from a systematic literature review of autosomal monosomy survivors. Prenat Diagn. 2017 12; 37(13):1273-1280.
    View in: PubMed
    Score: 0.204
  4. Dukhovny S, Wilkins-Haug L, Shipp TD, Benson CB, Kaimal AJ, Reiss R. Absent fetal nasal bone: what does it mean for the euploid fetus? J Ultrasound Med. 2013 Dec; 32(12):2131-4.
    View in: PubMed
    Score: 0.155
  5. Edlow AG, Reiss R, Benson CB, Gerrol P, Wilkins-Haug L. Monochorionic diamniotic twin gestations discordant for markedly enlarged nuchal translucency. Prenat Diagn. 2011 Mar; 31(3):299-306.
    View in: PubMed
    Score: 0.127
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.