Harvard Catalyst Profiles

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Raul Pina-Aguilar, M.D.

Title
Institution
Department
Address

Biography
2015
Fellowship in Infertility

Overview

Bibliographic
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. Piña-Aguilar RE, González-Ortega C, Calull-Bago A, Lanuza-López MC, Cancino-Villarreal P, Gutiérrez-Gamiño AM, Gutiérrez-Gutiérrez AM. [Combined Preimplantation Genetic Testing for Aneuploidy and Monogenic Disease in a Mexican Family Affected by X-linked Hypohidrotic Ectodermal Dysplasia]. Rev Invest Clin. 2018; 70(4):164-168. PMID: 30067729.
    Citations:    Fields:    Translation:Humans
  2. Redin C, Brand H, Collins RL, Kammin T, Mitchell E, Hodge JC, Hanscom C, Pillalamarri V, Seabra CM, Abbott MA, Abdul-Rahman OA, Aberg E, Adley R, Alcaraz-Estrada SL, Alkuraya FS, An Y, Anderson MA, Antolik C, Anyane-Yeboa K, Atkin JF, Bartell T, Bernstein JA, Beyer E, Blumenthal I, Bongers EM, Brilstra EH, Brown CW, Brüggenwirth HT, Callewaert B, Chiang C, Corning K, Cox H, Cuppen E, Currall BB, Cushing T, David D, Deardorff MA, Dheedene A, D'Hooghe M, de Vries BB, Earl DL, Ferguson HL, Fisher H, FitzPatrick DR, Gerrol P, Giachino D, Glessner JT, Gliem T, Grady M, Graham BH, Griffis C, Gripp KW, Gropman AL, Hanson-Kahn A, Harris DJ, Hayden MA, Hill R, Hochstenbach R, Hoffman JD, Hopkin RJ, Hubshman MW, Innes AM, Irons M, Irving M, Jacobsen JC, Janssens S, Jewett T, Johnson JP, Jongmans MC, Kahler SG, Koolen DA, Korzelius J, Kroisel PM, Lacassie Y, Lawless W, Lemyre E, Leppig K, Levin AV, Li H, Li H, Liao EC, Lim C, Lose EJ, Lucente D, Macera MJ, Manavalan P, Mandrile G, Marcelis CL, Margolin L, Mason T, Masser-Frye D, McClellan MW, Mendoza CJ, Menten B, Middelkamp S, Mikami LR, Moe E, Mohammed S, Mononen T, Mortenson ME, Moya G, Nieuwint AW, Ordulu Z, Parkash S, Pauker SP, Pereira S, Perrin D, Phelan K, Aguilar RE, Poddighe PJ, Pregno G, Raskin S, Reis L, Rhead W, Rita D, Renkens I, Roelens F, Ruliera J, Rump P, Schilit SL, Shaheen R, Sparkes R, Spiegel E, Stevens B, Stone MR, Tagoe J, Thakuria JV, van Bon BW, van de Kamp J, van Der Burgt I, van Essen T, van Ravenswaaij-Arts CM, van Roosmalen MJ, Vergult S, Volker-Touw CM, Warburton DP, Waterman MJ, Wiley S, Wilson A, Yerena-de Vega MC, Zori RT, Levy B, Brunner HG, de Leeuw N, Kloosterman WP, Thorland EC, Morton CC, Gusella JF, Talkowski ME. The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. Nat Genet. 2017 01; 49(1):36-45. PMID: 27841880.
    Citations: 14     Fields:    Translation:Humans
  3. Yokote K, Chanprasert S, Lee L, Eirich K, Takemoto M, Watanabe A, Koizumi N, Lessel D, Mori T, Hisama FM, Ladd PD, Angle B, Baris H, Cefle K, Palanduz S, Ozturk S, Chateau A, Deguchi K, Easwar TK, Federico A, Fox A, Grebe TA, Hay B, Nampoothiri S, Seiter K, Streeten E, Piña-Aguilar RE, Poke G, Poot M, Posmyk R, Martin GM, Kubisch C, Schindler D, Oshima J. WRN Mutation Update: Mutation Spectrum, Patient Registries, and Translational Prospects. Hum Mutat. 2017 01; 38(1):7-15. PMID: 27667302.
    Citations: 8     Fields:    Translation:HumansAnimals
  4. Piña-Aguilar RE, López-Saucedo J, Ruiz-Galaz LI, Barroso-Padilla JJ, Gallegos-Rivas MC, González-Ortega C, Gutiérrez-Gutiérrez AM. A human reproductive approach to the study of infertility in chimpanzees: An experience at Leon's Zoological Park, Mexico. Vet Res Forum. 2016; 7(3):255-259. PMID: 27872723.
    Citations:    
  5. González-Ortega C, Piña-Aguilar RE, Cancino-Villareal P, Gutiérrez-Gutiérrez AM. Birth after human chorionic gonadotropin-primed oocyte in vitro maturation and fertilization with testicular sperm in a normo-ovulatory patient. J Hum Reprod Sci. 2016 Jul-Sep; 9(3):210-212. PMID: 27803591.
    Citations:    
  6. Chacón-Camacho OF, Sobreira N, You J, Piña-Aguilar RE, Villegas-Ruiz V, Zenteno JC. Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndrome. Am J Med Genet A. 2016 07; 170(7):1934-7. PMID: 27139419.
    Citations: 1     Fields:    Translation:HumansCells
  7. Piña-Aguilar RE, Regalado-Hernández MÁ, Moreno-García JD, Buentello-Volante B, Chacón-Camacho OF, Gallegos-Rivas MC, Kazakova E, Santillán-Hernández Y, Zenteno JC. A rapidly progressive defective spermatogenesis in a Mexican family affected by spino-bulbar muscular atrophy. Syst Biol Reprod Med. 2016; 62(2):146-51. PMID: 26901084.
    Citations:    Fields:    Translation:HumansCells
  8. Santillán-Hernández Y, Almanza-Miranda E, Xin WW, Goss K, Vera-Loaiza A, Gorráez-de la Mora MT, Piña-Aguilar RE. Novel LIPA mutations in Mexican siblings with lysosomal acid lipase deficiency. World J Gastroenterol. 2015 Jan 21; 21(3):1001-8. PMID: 25624737.
    Citations: 2     Fields:    Translation:Humans
  9. Chacon-Camacho OF, Villegas-Ruiz V, Buentello-Volante B, Piña-Aguilar RE, Peláez-González H, Ramírez M, González-Rodríguez J, Zenteno JC. Acro-spondylo-pubic dysostosis associated with cataracts, microcephaly, and normal intelligence. Am J Med Genet A. 2015 Feb; 167A(2):282-6. PMID: 25427842.
    Citations:    Fields:    Translation:Humans
  10. Piña-Aguilar RE, Vera-Loaiza A, Chacón-Camacho OF, Zenteno JC, Nuñez-Orozco L, Santillán-Hernández Y. Clinical and genetic characteristics of mexican patients with juvenile presentation of niemann-pick type C disease. Case Rep Neurol Med. 2014; 2014:785890. PMID: 25349751.
    Citations: 2     
  11. Piña-Aguilar RE, Chima-Galán Mdel C, Yerena-de-vega Mde L, Regalado-Hernández MA, Sánchez-Guerrero C, García-Ortiz L, Santillán-Hernández Y, Moreno-García JD. [Genetic variants associated to male infertility in Mexican patients]. Ginecol Obstet Mex. 2013 May; 81(5):245-58. PMID: 23819425.
    Citations:    Fields:    Translation:HumansCells
  12. Chacon-Camacho OF, Lopez-Martinez MS, Vázquez J, Nava-Castañeda A, Martin-Biasotti F, Piña-Aguilar RE, Iñiguez-Soto M, Acosta-García J, Zenteno JC. Nasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic case. Am J Med Genet A. 2013 Jun; 161A(6):1470-4. PMID: 23636874.
    Citations: 3     Fields:    Translation:Humans
  13. Piña-Aguilar RE. Genetic screening in the American Society for Reproductive Medicine's new guidelines on diagnostic evaluation of the infertile male. Fertil Steril. 2013 Mar 01; 99(3):e9. PMID: 23337589.
    Citations:    Fields:    Translation:Humans
  14. Piña-Aguilar RE, Zaragoza-Arévalo GR, Rau I, Gal A, Alcántara-Ortigoza MA, López-Martínez MS, Santillán-Hernández Y. Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation. Eur J Med Genet. 2013 Mar; 56(3):159-62. PMID: 23232253.
    Citations: 4     Fields:    Translation:Humans
  15. López-Saucedo J, Paramio-Nieto MT, Fierro R, Piña-Aguilar RE. Intracytoplasmic sperm injection (ICSI) in small ruminants. Anim Reprod Sci. 2012 Aug; 133(3-4):129-38. PMID: 22871330.
    Citations: 2     Fields:    Translation:HumansAnimalsCells
  16. Piña-Aguilar RE, Martínez-Garza SG, Kohls G, Vargas-Maciel MA, Vázquez de Lara LG, González-Ortega C, Cancino-Villarreal P, Gutiérrez-Gutiérrez AM. Y chromosome microdeletions in Mexican males of couples with idiopathic recurrent pregnancy loss. J Obstet Gynaecol Res. 2012 Jun; 38(6):912-7. PMID: 22486969.
    Citations: 2     Fields:    Translation:HumansCells
  17. Piña-Aguilar RE. [Prevention of mitochondrial diseases: a hope through assisted reproductive technologies]. Gac Med Mex. 2011 Mar-Apr; 147(2):172-5. PMID: 21527975.
    Citations:    Fields:    Translation:Humans
  18. Piña-Aguilar RE, Lopez-Saucedo J, Sheffield R, Ruiz-Galaz LI, Barroso-Padilla Jde J, Gutiérrez-Gutiérrez A. Revival of extinct species using nuclear transfer: hope for the mammoth, true for the Pyrenean ibex, but is it time for "conservation cloning"? Cloning Stem Cells. 2009 Sep; 11(3):341-6. PMID: 19594389.
    Citations: 3     Fields:    Translation:HumansAnimalsCells
  19. Piña-Aguilar RE, Martínez-Garza SG, Gutiérrez-Gutiérrez AM. Are Y chromosome microdeletions and recurrent pregnancy loss really associated? Am J Obstet Gynecol. 2009 Nov; 201(5):e9; author reply e9-10. PMID: 19608147.
    Citations:    Fields:    Translation:HumansCells
  20. Herrera-Najera C, Piña-Aguilar R, Xacur-Garcia F, Ramirez-Sierra MJ, Dumonteil E. Mining the Leishmania genome for novel antigens and vaccine candidates. Proteomics. 2009 Mar; 9(5):1293-301. PMID: 19206109.
    Citations: 16     Fields:    Translation:HumansAnimalsCellsPHPublic Health
  21. Piña-Aguilar RE. Bringing together clinical embryology and basic reproduction around human cloning. Hum Reprod. 2008 Dec; 23(12):2875-6. PMID: 18854407.
    Citations:    Fields:    Translation:Humans
  22. Piña-Aguilar RE. [The clinician's importance in the development of stem cell therapies]. Rev Med Chil. 2007 Aug; 135(8):1084-6. PMID: 17989870.
    Citations:    Fields:    Translation:HumansCells
  23. Piña-Aguilar RE. [Functional genomics in single embryo and human oocytes]. Gac Med Mex. 2007 Jan-Feb; 143(1):89-91. PMID: 17388102.
    Citations:    Fields:    Translation:HumansCells
  24. Piña-Aguilar RE. The future of sperm-derived mRNAs. Fertil Steril. 2006 Sep; 86(3):775-6; author reply 776-7. PMID: 16952528.
    Citations:    Fields:    Translation:HumansCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.