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Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma
Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma
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Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma

KRAUTHAMMER, Michael ; YONGKONG ; ARIYAN, Stephan ; NARAYAN, Deepak ; DUTTON-REGESTER, Ken ; CAPATANA, Ana ; HOLMAN, Edna C ; BOSENBERG, Marcus ; SZNOL, Mario ; KLUGER, Harriet M ; BRASH, Douglas E ; STERN, David F ; BYUNGHAKHA ; MATERIN, Miguel A ; LO, Roger S ; MANE, Shrikant ; SHUANGGE MA ; KIDD, Kenneth K ; HAYWARD, Nicholas K ; LIFTON, Richard P ; SCHLESSINGER, Joseph ; BOGGON, Titus J ; HALABAN, Ruth ; EVANS, Perry ; BACCHIOCCHI, Tonella ; MCCUSKER, James P ; CHENG, Elaine ; DAVIS, Matthew J ; GOH, Gerald ; CHOI, Murim

Nature genetics, 2012-09, Vol.44 (9), p.1006-1014 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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2
Exaggerated phase–amplitude coupling in the primary motor cortex in Parkinson disease
Exaggerated phase–amplitude coupling in the primary motor cortex in Parkinson disease
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Exaggerated phase–amplitude coupling in the primary motor cortex in Parkinson disease

de Hemptinne, Coralie ; Ryapolova-Webb, Elena S. ; Air, Ellen L. ; Garcia, Paul A. ; Miller, Kai J. ; Ojemann, Jeffrey G. ; Ostrem, Jill L. ; Galifianakis, Nicholas B. ; Starr, Philip A.

Proceedings of the National Academy of Sciences - PNAS, 2013-03, Vol.110 (12), p.4780-4785 [Periódico revisado por pares]

Washington, DC: National Academy of Sciences

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3
Intrinsic connectivity networks in healthy subjects explain clinical variability in Alzheimer’s disease
Intrinsic connectivity networks in healthy subjects explain clinical variability in Alzheimer’s disease
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Intrinsic connectivity networks in healthy subjects explain clinical variability in Alzheimer’s disease

Lehmann, Manja ; Madison, Cindee M. ; Ghosh, Pia M. ; Seeley, William W. ; Mormino, Elizabeth ; Greicius, Michael D. ; Gorno-Tempini, Maria Luisa ; Kramer, Joel H. ; Miller, Bruce L. ; Jagust, William J. ; Rabinovici, Gil D.

Proceedings of the National Academy of Sciences - PNAS, 2013-07, Vol.110 (28), p.11606-11611 [Periódico revisado por pares]

Washington, DC: National Academy of Sciences

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4
Simple Cystatin C-Based Prediction Equations for Glomerular Filtration Rate Compared with the Modification of Diet in Renal Disease Prediction Equation for Adults and the Schwartz and the Counahan-Barratt Prediction Equations for Children
Simple Cystatin C-Based Prediction Equations for Glomerular Filtration Rate Compared with the Modification of Diet in Renal Disease Prediction Equation for Adults and the Schwartz and the Counahan-Barratt Prediction Equations for Children
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Simple Cystatin C-Based Prediction Equations for Glomerular Filtration Rate Compared with the Modification of Diet in Renal Disease Prediction Equation for Adults and the Schwartz and the Counahan-Barratt Prediction Equations for Children

Grubb, Anders ; Nyman, Ulf ; Bjork, Jonas ; Lindstrom, Veronica ; Rippe, Bengt ; Sterner, Gunnar ; Christensson, Anders

Clinical chemistry (Baltimore, Md.), 2005-08, Vol.51 (8), p.1420-1431 [Periódico revisado por pares]

Washington, DC: Am Assoc Clin Chem

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5
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes
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Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes

Jaiswal, Siddhartha ; Fontanillas, Pierre ; Flannick, Jason ; Manning, Alisa ; Grauman, Peter V ; Mar, Brenton G ; Lindsley, R. Coleman ; Mermel, Craig H ; Burtt, Noel ; Chavez, Alejandro ; Higgins, John M ; Moltchanov, Vladislav ; Kuo, Frank C ; Kluk, Michael J ; Henderson, Brian ; Kinnunen, Leena ; Koistinen, Heikki A ; Ladenvall, Claes ; Getz, Gad ; Correa, Adolfo ; Banahan, Benjamin F ; Gabriel, Stacey ; Kathiresan, Sekar ; Stringham, Heather M ; McCarthy, Mark I ; Boehnke, Michael ; Tuomilehto, Jaakko ; Haiman, Christopher ; Groop, Leif ; Atzmon, Gil ; Wilson, James G ; Neuberg, Donna ; Altshuler, David ; Ebert, Benjamin L

The New England journal of medicine, 2014-12, Vol.371 (26), p.2488-2498 [Periódico revisado por pares]

Waltham, MA: Massachusetts Medical Society

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6
A task to assess behavioral pattern separation (BPS) in humans: Data from healthy aging and mild cognitive impairment
A task to assess behavioral pattern separation (BPS) in humans: Data from healthy aging and mild cognitive impairment
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A task to assess behavioral pattern separation (BPS) in humans: Data from healthy aging and mild cognitive impairment

Stark, Shauna M. ; Yassa, Michael A. ; Lacy, Joyce W. ; Stark, Craig E.L.

Neuropsychologia, 2013-10, Vol.51 (12), p.2442-2449 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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7
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
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Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence

Genovese, Giulio ; Kähler, Anna K ; Handsaker, Robert E ; Lindberg, Johan ; Rose, Samuel A ; Bakhoum, Samuel F ; Chambert, Kimberly ; Mick, Eran ; Neale, Benjamin M ; Fromer, Menachem ; Purcell, Shaun M ; Svantesson, Oscar ; Landén, Mikael ; Höglund, Martin ; Lehmann, Sören ; Gabriel, Stacey B ; Moran, Jennifer L ; Lander, Eric S ; Sullivan, Patrick F ; Sklar, Pamela ; Grönberg, Henrik ; Hultman, Christina M ; McCarroll, Steven A

The New England journal of medicine, 2014-12, Vol.371 (26), p.2477-2487 [Periódico revisado por pares]

Waltham, MA: Massachusetts Medical Society

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8
Age Group Comparability of Raw Accelerometer Output from Wrist- and Hip-Worn Monitors
Age Group Comparability of Raw Accelerometer Output from Wrist- and Hip-Worn Monitors
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Age Group Comparability of Raw Accelerometer Output from Wrist- and Hip-Worn Monitors

HILDEBRAND, MARIA ; VAN HEES, VINCENT T ; HANSEN, BJORGE HERMANN ; EKELUND, ULF

Medicine and science in sports and exercise, 2014-09, Vol.46 (9), p.1816-1824 [Periódico revisado por pares]

Hagerstown, MD: American College of Sports Medicine

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9
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
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Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2

LEMMERS, Richard J. L. F ; TAWIL, Rabi ; KROM, Yvonne D ; KLOOSTER, Rinse ; YU SUN ; DEN DUNNEN, Johan T ; HELMER, Quinta ; DONLIN-SMITH, Colleen M ; PADBERG, George W ; VAN ENGELEN, Baziel G. M ; DE GREEF, Jessica C ; AARTSMA-RUS, Annemieke M ; PETEK, Lisa M ; FRANTS, Rune R ; DE VISSER, Marianne ; DESNUELLE, Claude ; SACCONI, Sabrina ; FILIPPOVA, Galina N ; BAKKER, Bert ; BAMSHAD, Michael J ; TAPSCOTT, Stephen J ; MILLER, Daniel G ; VAN DER MAAREL, Silvere M ; BALOG, Judit ; BLOCK, Gregory J ; SANTEN, Gijs W. E ; AMELL, Amanda M ; VAN DER VLIET, Patrick J ; ALMOMANI, Rowida ; STRAASHEIJM, Kirsten R

Nature genetics, 2012-12, Vol.44 (12), p.1370-1374 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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10
Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)
Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)
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Clinical Practice Guidelines for Multiple Endocrine Neoplasia Type 1 (MEN1)

Thakker, Rajesh V ; Newey, Paul J ; Walls, Gerard V ; Bilezikian, John ; Dralle, Henning ; Ebeling, Peter R ; Melmed, Shlomo ; Sakurai, Akihiro ; Tonelli, Francesco ; Brandi, Maria Luisa

The journal of clinical endocrinology and metabolism, 2012-09, Vol.97 (9), p.2990-3011 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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