TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Molecular & Human Genetics
Address2450 HOLCOMBE
Houston, TX 77021
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    Other Positions
    TitleAssistant Professor
    InstitutionBaylor College of Medicine
    DepartmentDepartment of Obstetrics & Gynecology
    DivisionObstetrics and Gynecology

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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Wang H, Page R, Lopez D, Arkatkar S, Young C, Martinez D, Robbins-Furman P, Montalvo-Liendo N, Chen LS. Pregnant Latinas' views of adopting exome sequencing into newborn screening: A qualitative study. Genet Med. 2022 May 17. PMID: 35579624.
      Citations:    Fields:    
    2. Wu KL, Alegria R, Gonzalez J, Hu H, Wang H, Page R, Robbins-Furman P, Ma P, Tseng TS, Chen LS. Characteristics and Quality of Mobile Apps Containing Prenatal Genetic Testing Information: Systematic App Store Search and Assessment. JMIR Mhealth Uhealth. 2021 10 14; 9(10):e30404. PMID: 34647898.
      Citations:    Fields:    Translation:Humans
    3. Young C, Wang H, Martinez D, Chen WJ, Page R, Robbins-Furman P, Montalvo-Liendo N, Williamson B, Chen LS. Rural, Low-Income, Pregnant Latina Women's Perspectives on Carrier Screening. Obstet Gynecol. 2021 07 01; 138(1):106-107. PMID: 34259471.
      Citations:    Fields:    Translation:Humans
    4. Grygiel A, Ikolo F, Stephen R, Bleasdille D, Robbins-Furman P, Nelson B, Sobering AK, Elsea SH. Sickle cell disease in Grenada: Quality of life and barriers to care. Mol Genet Genomic Med. 2021 01; 9(1):e1567. PMID: 33332776.
      Citations:    Fields:    Translation:Humans
    5. Carter RD, Raia M, Ewing-Cobbs L, Gambello M, Hashmi SS, Peterson SK, Robbins-Furman P, Potocki L. Stress and well-being among parents of children with Potocki-Lupski syndrome. J Genet Couns. 2013 Oct; 22(5):633-42. PMID: 23709095.
      Citations: 4     Fields:    Translation:Humans
    6. Jefferies JL, Pignatelli RH, Martinez HR, Robbins-Furman PJ, Liu P, Gu W, Lupski JR, Potocki L. Cardiovascular findings in duplication 17p11.2 syndrome. Genet Med. 2012 Jan; 14(1):90-4. PMID: 22237436.
      Citations: 14     Fields:    Translation:Humans
    7. Andrabi S, Bekheirnia MR, Robbins-Furman P, Lewis RA, Prior TW, Potocki L. SMAD4 mutation segregating in a family with juvenile polyposis, aortopathy, and mitral valve dysfunction. Am J Med Genet A. 2011 May; 155A(5):1165-9. PMID: 21465659.
      Citations: 31     Fields:    Translation:Humans
    8. Soler-Alfonso C, Motil KJ, Turk CL, Robbins-Furman P, Friedman EM, Zhang F, Lupski JR, Fraley JK, Potocki L. Potocki-Lupski syndrome: a microduplication syndrome associated with oropharyngeal dysphagia and failure to thrive. J Pediatr. 2011 Apr; 158(4):655-659.e2. PMID: 21168152.
      Citations: 20     Fields:    Translation:Humans
    9. Zhang F, Potocki L, Sampson JB, Liu P, Sanchez-Valle A, Robbins-Furman P, Navarro AD, Wheeler PG, Spence JE, Brasington CK, Withers MA, Lupski JR. Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS. Am J Hum Genet. 2010 Mar 12; 86(3):462-70. PMID: 20188345.
      Citations: 43     Fields:    Translation:HumansCells
    10. Dhar SU, Robbins-Furman P, Levy ML, Patel A, Scaglia F. Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty. Am J Med Genet A. 2009 May; 149A(5):993-6. PMID: 19334087.
      Citations: 2     Fields:    Translation:HumansCells
    11. Hoskovec J, Mastrobattista JM, Johnston D, Kerrigan A, Robbins-Furman P, Wicklund CA. Anxiety and prenatal testing: do women with soft ultrasound findings have increased anxiety compared to women with other indications for testing? Prenat Diagn. 2008 Feb; 28(2):135-40. PMID: 18236427.
      Citations: 9     Fields:    Translation:Humans
    12. Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, Glaze D, Krull K, Lee JA, Lewis RA, Mendoza-Londono R, Robbins-Furman P, Shaw C, Shi X, Weissenberger G, Withers M, Yatsenko SA, Zackai EH, Stankiewicz P, Lupski JR. Characterization of Potocki-Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. Am J Hum Genet. 2007 Apr; 80(4):633-49. PMID: 17357070.
      Citations: 141     Fields:    Translation:HumansCells
    13. Saucier JB, Johnston D, Wicklund CA, Robbins-Furman P, Hecht JT, Monga M. Racial-ethnic differences in genetic amniocentesis uptake. J Genet Couns. 2005 Jun; 14(3):189-95. PMID: 15959650.
      Citations: 10     Fields:    Translation:Humans
    14. Harris A, Monga M, Wicklund CA, Robbins-Furman PJ, Strecker MN, Doyle NM, Mastrobattista J. Clinical correlates of pain with amniocentesis. Am J Obstet Gynecol. 2004 Aug; 191(2):542-5. PMID: 15343234.
      Citations: 1     Fields:    Translation:Humans
    15. Robbins-Furman P, Hecht JT, Rocklin M, Maklad N, Greenhaw G, Wilkins I. Prenatal diagnosis of Freeman-Sheldon syndrome (whistling face). Prenat Diagn. 1995 Feb; 15(2):179-82. PMID: 7784371.
      Citations: 2     Fields:    Translation:Humans
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