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Reply to Pisan et al.: Pathogenicity of inherited TRAF7 mutations in congenital heart disease.
Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2319578121. doi: 10.1073/pnas.2319578121. Epub 2024 Mar 11.
Proc Natl Acad Sci U S A. 2024.
PMID: 38466853
Free PMC article.
No abstract available.
Illness Perception and the Impact of a Definitive Diagnosis on Women With Ischemia and No Obstructive Coronary Artery Disease: A Qualitative Study.
Tseng LY, Göç N, Schwann AN, Cherlin EJ, Kunnirickal SJ, Odanovic N, Curry LA, Shah SM, Spatz ES.
Tseng LY, et al. Among authors: goc n.
Circ Cardiovasc Qual Outcomes. 2023 Aug;16(8):521-529. doi: 10.1161/CIRCOUTCOMES.122.009834. Epub 2023 Jul 21.
Circ Cardiovasc Qual Outcomes. 2023.
PMID: 37476997
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Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease.
Mishra-Gorur K, Barak T, Kaulen LD, Henegariu O, Jin SC, Aguilera SM, Yalbir E, Goles G, Nishimura S, Miyagishima D, Djenoune L, Altinok S, Rai DK, Viviano S, Prendergast A, Zerillo C, Ozcan K, Baran B, Sencar L, Goc N, Yarman Y, Ercan-Sencicek AG, Bilguvar K, Lifton RP, Moliterno J, Louvi A, Yuan S, Deniz E, Brueckner M, Gunel M.
Mishra-Gorur K, et al. Among authors: goc n.
Proc Natl Acad Sci U S A. 2023 Apr 18;120(16):e2214997120. doi: 10.1073/pnas.2214997120. Epub 2023 Apr 12.
Proc Natl Acad Sci U S A. 2023.
PMID: 37043537
Free PMC article.
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Strengthening Public Health Scholarship in Sudan: The Role of Leadership and Mentorship Development.
Göç N, Hassan S, Bani I, Babiker S, Hilali M, Ibrahim Z, Gaddal A, Saleh L, Salih EM, Desai MM, Linnander E.
Göç N, et al.
Am J Trop Med Hyg. 2022 Nov 7;107(6):1323-1330. doi: 10.4269/ajtmh.22-0377. Print 2022 Dec 14.
Am J Trop Med Hyg. 2022.
PMID: 36343591
Free PMC article.
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Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM.
Tüysüz B, Ercan-Sençicek AG, Özer E, Göç N, Yalçınkaya C, Bilguvar K.
Tüysüz B, et al. Among authors: goc n.
Turk Arch Pediatr. 2022 Sep;57(5):521-525. doi: 10.5152/TurkArchPediatr.2022.22070.
Turk Arch Pediatr. 2022.
PMID: 35950747
Free PMC article.
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PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans.
Barak T, Ristori E, Ercan-Sencicek AG, Miyagishima DF, Nelson-Williams C, Dong W, Jin SC, Prendergast A, Armero W, Henegariu O, Erson-Omay EZ, Harmancı AS, Guy M, Gültekin B, Kilic D, Rai DK, Goc N, Aguilera SM, Gülez B, Altinok S, Ozcan K, Yarman Y, Coskun S, Sempou E, Deniz E, Hintzen J, Cox A, Fomchenko E, Jung SW, Ozturk AK, Louvi A, Bilgüvar K, Connolly ES Jr, Khokha MK, Kahle KT, Yasuno K, Lifton RP, Mishra-Gorur K, Nicoli S, Günel M.
Barak T, et al. Among authors: goc n.
Nat Med. 2021 Dec;27(12):2165-2175. doi: 10.1038/s41591-021-01572-7. Epub 2021 Dec 9.
Nat Med. 2021.
PMID: 34887573
Free PMC article.
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Strengthening the Mentorship and Leadership Capacity of HIV/AIDS and Tuberculosis Researchers in South Africa.
Desai MM, Göç N, Chirwa T, Manderson L, Charalambous S, Curry LA, Linnander E.
Desai MM, et al. Among authors: goc n.
Am J Trop Med Hyg. 2021 Aug 16;105(5):1317-1325. doi: 10.4269/ajtmh.21-0072.
Am J Trop Med Hyg. 2021.
PMID: 34398822
Free PMC article.
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Novel compound heterozygous mutations in GPT2 linked to microcephaly, and intellectual developmental disability with or without spastic paraplegia.
Kaymakcalan H, Yarman Y, Goc N, Toy F, Meral C, Ercan-Sencicek AG, Gunel M.
Kaymakcalan H, et al. Among authors: goc n.
Am J Med Genet A. 2018 Feb;176(2):421-425. doi: 10.1002/ajmg.a.38558. Epub 2017 Dec 11.
Am J Med Genet A. 2018.
PMID: 29226631
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