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    {
        "title": "Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.",
        "journal": "Am. J. Med. Genet. B Neuropsychiatr. Genet.",
        "date": "2006",
        "authors": "Durand Christelle M, Kappeler Caroline, Betancur Catalina, Delorme Richard, Quach H\u00e9l\u00e8ne, Goubran-Botros Hany, Melke Jonas, Nygren Gudrun, Chabane Nadia, Bellivier Franck, Szoke Andrei, Schurhoff Franck, Rastam Maria, Anckars\u00e4ter Henrik, Gillberg Christopher, Leboyer Marion, Bourgeron Thomas",
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        ],
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    {
        "title": "Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux.",
        "journal": "Am. J. Hum. Genet.",
        "date": "2007",
        "authors": "Lu W, van Eerde AM, Fan X, Quintero-Rivera F, Kulkarni S, Ferguson H, Kim HG, Fan Y, Xi Q, Li QG, Sanlaville D, Andrews W, Sundaresan V, Bi W, Yan J, Giltay JC, Wijmenga C, de Jong TP, Feather SA, Woolf AS, Rao Y, Lupski JR, Eccles MR, Quade BJ, Gusella JF, Morton CC, Maas RL",
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                                "id": "MONDO:0014422",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0014422",
                                "name": "vesicoureteral reflux (disease) caused by mutation in TNXB",
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                                "id": "MONDO:0044660",
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                                "id": "MONDO:0044660",
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