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Machine Learning (ML) based-method applied in recurrent pregnancy loss (RPL) patients diagnostic work-up: a potential innovation in common clinical practice
Machine Learning (ML) based-method applied in recurrent pregnancy loss (RPL) patients diagnostic work-up: a potential innovation in common clinical practice
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Machine Learning (ML) based-method applied in recurrent pregnancy loss (RPL) patients diagnostic work-up: a potential innovation in common clinical practice

Bruno, V ; D'Orazio, M ; Ticconi, C ; Abundo, P ; Riccio, S ; Martinelli, E ; Rosato, N ; Piccione, E ; Zupi, E ; Pietropolli, A

Scientific reports, 2020-05, Vol.10 (1), p.7970-7970, Article 7970 [Periódico revisado por pares]

England: Nature Publishing Group

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2
CXCR4 and CXCR7 transduce through mTOR in human renal cancer cells
CXCR4 and CXCR7 transduce through mTOR in human renal cancer cells
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CXCR4 and CXCR7 transduce through mTOR in human renal cancer cells

Ieranò, C ; Santagata, S ; Napolitano, M ; Guardia, F ; Grimaldi, A ; Antignani, E ; Botti, G ; Consales, C ; Riccio, A ; Nanayakkara, M ; Barone, M V ; Caraglia, M ; Scala, S

Cell death & disease, 2014-07, Vol.5 (7), p.e1310-e1310 [Periódico revisado por pares]

England: Springer Nature B.V

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3
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome
Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome
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Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome

COOPER, Wendy N ; LUHARIA, Anita ; SCHOFIELD, Paul N ; REIK, Wolf ; MACDONALD, Fiona ; MAHER, Eamonn R ; EVANS, Gail A ; RAZA, Hussain ; HAIRE, Antonita C ; GRUNDY, Richard ; BOWDIN, Sarah C ; RICCIO, Andrea ; SEBASTIO, Gianfranco ; BLIEK, Jet

European journal of human genetics : EJHG, 2005-09, Vol.13 (9), p.1025-1032 [Periódico revisado por pares]

Avenel, NJ: Nature Publishing

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4
Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort
Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort
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Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort

Nagar, Shashwat Deepali ; Pemu, Priscilla ; Qian, Jun ; Boerwinkle, Eric ; Cicek, Mine ; Clark, Cheryl R ; Cohn, Elizabeth ; Gebo, Kelly ; Loperena, Roxana ; Mayo, Kelsey ; Mockrin, Stephen ; Ohno-Machado, Lucila ; Ramirez, Andrea H ; Schully, Sheri ; Able, Ashley ; Green, Ashley ; Zuchner, Stephan ; Jordan, I King ; Meller, Robert

Scientific reports, 2022-11, Vol.12 (1), p.19797-19797, Article 19797 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry
Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry
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Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry

Kessler, Michael D ; Yerges-Armstrong, Laura ; Taub, Margaret A ; Shetty, Amol C ; Maloney, Kristin ; Jeng, Linda Jo Bone ; Ruczinski, Ingo ; Levin, Albert M ; Williams, L Keoki ; Beaty, Terri H ; Mathias, Rasika A ; Barnes, Kathleen C ; O'Connor, Timothy D

Nature communications, 2016-10, Vol.7 (1), p.12521-12521, Article 12521 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome
Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome
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Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome

Johnston, Henry Richard ; Hu, Yi-Juan ; Gao, Jingjing ; O'Connor, Timothy D ; Abecasis, Gonçalo R ; Wojcik, Genevieve L ; Gignoux, Christopher R ; Gourraud, Pierre-Antoine ; Lizee, Antoine ; Hansen, Mark ; Genuario, Rob ; Bullis, Dave ; Lawley, Cindy ; Kenny, Eimear E ; Bustamante, Carlos ; Beaty, Terri H ; Mathias, Rasika A ; Barnes, Kathleen C ; Qin, Zhaohui S

Scientific reports, 2017-04, Vol.7 (1), p.46398-46398, Article 46398 [Periódico revisado por pares]

England: Nature Publishing Group

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7
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation
Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation
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Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation

Mirghomizadeh, Farhad ; Bardtke, Bettina ; Devoto, Marcella ; Pfister, Markus ; Oeken, Jens ; König, Elke ; Vitale, Emilia ; Riccio, Antonio ; De Rienzo, Assunta ; Zenner, Hans Peter ; Blin, Nikolaus

European journal of human genetics : EJHG, 2002-02, Vol.10 (2), p.95-99 [Periódico revisado por pares]

England: Nature Publishing Group

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