Ryan P. Hillary
Stanford University
12 Papers
31 Citations
Ryan P. Hillary is an academic researcher from Stanford University. The author has contributed to research in topics: Medicine & Genome-wide association study. The author has an hindex of 6, co-authored 10 publications.
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Papers
The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight.
Francine E. Garrett-Bakelman,Francine E. Garrett-Bakelman,Manjula Darshi,Stefan J. Green,Ruben C. Gur,Ling Lin,Brandon R. Macias,Miles J. McKenna,Cem Meydan,Tejaswini Mishra,Jad Nasrini,Brian D. Piening,Brian D. Piening,Lindsay F. Rizzardi,Kumar Sharma,Jamila H. Siamwala,Jamila H. Siamwala,Lynn Taylor,Martha Hotz Vitaterna,Maryam Afkarian,Ebrahim Afshinnekoo,Sara Ahadi,Aditya Ambati,Maneesh Arya,Daniela Bezdan,Colin M. Callahan,Songjie Chen,Augustine M.K. Choi,George E. Chlipala,Kévin Contrepois,Marisa Covington,Brian Crucian,Immaculata De Vivo,David F. Dinges,Douglas J. Ebert,Jason I. Feinberg,Jorge Gandara,Kerry George,John Goutsias,George Grills,Alan R. Hargens,Martina Heer,Martina Heer,Ryan P. Hillary,Andrew N. Hoofnagle,Vivian Hook,Garrett Jenkinson,Garrett Jenkinson,Peng Jiang,Ali Keshavarzian,Steven S. Laurie,Brittany Lee-McMullen,Sarah B. Lumpkins,Matthew MacKay,Mark Maienschein-Cline,Ari Melnick,Tyler M. Moore,Kiichi Nakahira,Hemal H. Patel,Robert Pietrzyk,Varsha Rao,Rintaro Saito,Rintaro Saito,Denis Salins,Jan M. Schilling,Dorothy D. Sears,Caroline Sheridan,Michael B. Stenger,Rakel Tryggvadottir,Alexander E. Urban,Tomas Vaisar,Benjamin Van Espen,Jing Zhang,Michael G. Ziegler,Sara R. Zwart,John B. Charles,Craig E. Kundrot,Graham B. I. Scott,Susan M. Bailey,Mathias Basner,Andrew P. Feinberg,Stuart M. C. Lee,Christopher E. Mason,Emmanuel Mignot,Brinda K. Rana,Scott M. Smith,Michael Snyder,Fred W. Turek,Fred W. Turek +88 more
TL;DR: Given that the majority of the biological and human health variables remained stable, or returned to baseline, after a 340-day space mission, these data suggest that human health can be mostly sustained over this duration of spaceflight.
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Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases A Mendelian Randomization Study
Philip C Haycock,Stephen Burgess,Aayah Nounu,Jie Zheng,G N Okoli,Jack Bowden,Kaitlin H Wade,Nicholas J. Timpson,David M. Evans,Peter Willeit,Abraham Aviv,Tom R. Gaunt,Gibran Hemani,Massimo Mangino,Hayley P Ellis,Kathreena M Kurian,Karen A. Pooley,Rosalind A. Eeles,Jeffrey E. Lee,Shenying Fang,Wei V. Chen,Matthew Law,Lisa Bowdler,Mark M. Iles,Qiong Yang,Bradford B. Worrall,Hugh S. Markus,Rayjean J. Hung,Christopher I. Amos,Amanda B. Spurdle,Deborah J. Thompson,Tracy A. O'Mara,Brian M. Wolpin,Laufey T. Amundadottir,Rachael Z. Stolzenberg-Solomon,Antonia Trichopoulou,N. Charlotte Onland-Moret,Eiliv Lund,Eric J. Duell,Federico Canzian,Gianluca Severi,Kim Overvad,Marc J. Gunter,Rosario Tumino,Ulrika Svenson,Andre M. van Rij,Annette F. Baas,Matthew J. Bown,Nilesh J. Samani,Femke N G van t'Hof,Gerard Tromp,Gregory T. Jones,Helena Kuivaniemi,James R. Elmore,Mattias Johansson,James McKay,Ghislaine Scelo,Robert Carreras-Torres,Valerie Gaborieau,Paul Brennan,Paige M. Bracci,Rachel E. Neale,Sara H. Olson,Steven Gallinger,Donghui Li,Gloria M. Petersen,Harvey A. Risch,Alison P. Klein,Jiali Han,Christian C. Abnet,Neal D. Freedman,Philip R. Taylor,John M. Maris,Katja K.H. Aben,Lambertus A. Kiemeney,Sita H. Vermeulen,John K. Wiencke,Kyle M. Walsh,Margaret Wrensch,Terri Rice,Clare Turnbull,Kevin Litchfield,Lavinia Paternoster,Marie Standl,Gonçalo R. Abecasis,John Paul SanGiovanni,Yong Li,Vladan Mijatovic,Yadav Sapkota,Siew-Kee Low,Krina T. Zondervan,Grant W. Montgomery,Dale R. Nyholt,David A. van Heel,Karen A. Hunt,Dan E. Arking,Foram N. Ashar,Nona Sotoodehnia,Daniel Woo,Jonathan Rosand,Mary E. Comeau,W. Mark Brown,Edwin K. Silverman,John E. Hokanson,Michael H. Cho,Jennie Hui,Manuel A. R. Ferreira,Philip J. Thompson,Alanna C. Morrison,Janine F. Felix,Nicholas L. Smith,Angela M. Christiano,Lynn Petukhova,Regina C. Betz,Xing Fan,Xuejun Zhang,Caihong Zhu,Carl D. Langefeld,Susan D. Thompson,Feijie Wang,Xu Lin,David A. Schwartz,Tasha E. Fingerlin,Jerome I. Rotter,Mary Frances Cotch,Richard A. Jensen,Matthias Munz,Henrik Dommisch,Arne S. Schaefer,Fang Han,Hanna Ollila,Ryan P. Hillary,Omar M. E. Albagha,Stuart H. Ralston,Chenjie Zeng,Wei Zheng,Xiao-Ou Shu,André Reis,Steffen Uebe,Ulrike Hüffmeier,Yoshiya Kawamura,Takeshi Otowa,Tsukasa Sasaki,Martin L. Hibberd,Sonia Davila,Gang Xie,Katherine A. Siminovitch,Jin-Xin Bei,Yi Xin Zeng,Asta Försti,Bowang Chen,Stefano Landi,Andre Franke,Annegret Fischer,David Ellinghaus,Carlos Flores,Imre Noth,Shwu-Fan Ma,Jia Nee Foo,Jianjun Liu,Jong-Won Kim,David G. Cox,Olivier Delattre,Olivier Mirabeau,Christine F. Skibola,Clara S. Tang,Merce Garcia-Barcelo,Kai-Ping Chang,Wen-Hui Su,Yu-Sun Chang,Nicholas G. Martin,Scott D. Gordon,Tracey D. Wade,Chaeyoung Lee,Michiaki Kubo,Pei-Chieng Cha,Yusuke Nakamura,Daniel Levy,Masayuki Kimura,Shih-Jen Hwang,Steven C. Hunt,Tim D. Spector,Nicole Soranzo,Ani Manichaikul,R. Graham Barr,Bratati Kahali,Elizabeth K. Speliotes,Laura M. Yerges-Armstrong,Ching-Yu Cheng,Jost B. Jonas,Tien Yin Wong,Isabella Fogh,Kuang Lin,John Powell,Kenneth Rice,Caroline L Relton,Richard M. Martin,George Davey Smith +197 more
TL;DR: It is likely that longer telomeres increase risk for several cancers but reduce risk for some non-neoplastic diseases, including cardiovascular diseases, as well as single nucleotide polymorphisms (SNPs) that are strongly associated with telomere length in the general population.
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci
Aditya Ambati,Ryan P. Hillary,Smaranda Leu-Semenescu,Hanna Ollila,Ling Lin,Emmanuel H. During,Neal M. Farber,Thomas J Rico,Juliette Faraco,Eileen B. Leary,Andrea N. Goldstein-Piekarski,Andrea N. Goldstein-Piekarski,Yu-Shu Huang,Fang Han,Yakov Sivan,Michel Lecendreux,Pauline Dodet,Makoto Honda,Natan Gadoth,Sona Nevsimalova,Fabio Pizza,Takashi Kanbayashi,Rosa Peraita-Adrados,Guy D. Leschziner,Rosa Hasan,Francesca Canellas,Kazuhiko Kume,Makrina Daniilidou,Patrice Bourgin,David B. Rye,José L. Vicario,Birgit Högl,Seung Chul Hong,G. Plazzi,Geert Mayer,Anne-Marie Landtblom,Anne-Marie Landtblom,Yves Dauvilliers,Isabelle Arnulf,Emmanuel Mignot +39 more
TL;DR: The authors found a strong genome-wide significant association (rs71947865, Odds Ratio [OR] = 1.48, P = 8.6 × 10-9) within the 3'gion of TRANK1 gene locus, previously associated with bipolar disorder and schizophrenia.
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Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
Hanna Ollila,Eilon Sharon,Ling Lin,Nasa Sinnott-Armstrong,Aditya Ambati,S. Yogeshwar,Ryan P. Hillary,Otto Jolanki,Juliette Faraco,Mali Einen,Guo Luo,Jing Zhang,Fang Han,Han Yan,Xiao Song Dong,Jing Li,Jun Zhang,Seung Chul Hong,Tae-Won Kim,Yves Dauvilliers,Lucie Barateau,Gert Jan Lammers,Rolf Fronczek,Geert Mayer,Joan Santamaria,Isabelle Arnulf,Stine Knudsen-Heier,May Kristin Lyamouri Bredahl,Per Medbøe Thorsby,Giuseppe Plazzi,Fabio Pizza,Monica Moresco,C. Crowe,Stephen K. Van Den Eeden,Michel Lecendreux,Patrice Bourgin,Takashi Kanbayashi,Francisco J. Martínez-Orozco,Rosa Peraita-Adrados,Antonio Benetó,Jacques Montplaisir,Alex Desautels,Yu-Shu Huang,Poul Jennum,Sona Nevsimalova,David Kemlink,Alex Iranzo,Sebastiaan Overeem,Aleksandra Wierzbicka,Peter Geisler,Karel Sonka,Makoto Honda,Birgit Högl,Ambra Stefani,Fernando M. S. Coelho,Vilma Mantovani,Eva Feketeova,Mia Wadelius,Nicholas Eriksson,Hans Smedje,Pär Hallberg,Per Egil Hesla,David Rye,Zerrin Pelin,Luigi Ferini-Strambi,Claudio L. Bassetti,Johannes Mathis,Ramin Khatami,Adi Aran,Sheela Nampoothiri,Tomas Olsson,Ingrid Kockum,Markku Partinen,Markus Perola,Birgitte Rahbek Kornum,S.A. Rueger,Juliane Winkelmann,Taku Miyagawa,Hiromi Toyoda,Seik-Soon Khor,Mihoko Shimada,Katsushi Tokunaga,M. Rivas,Jonathan K. Pritchard,Neil Risch,Zoltán Kutalik,Ruth O’Hara,Joachim Hallmayer,Chun Ye,Emmanuel Mignot +89 more
TL;DR: In this article , the authors fine-mapped GWAS signals within HLA (DQ0602, DQB1*03:01 and DPB1*04:02) and discovered seven novel associations (CD207, NAB1, IKZF4-ERBB3, CTSC, DENND1B, SIRPG, PRF1).
Kleine Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci.
Aditya Ambati,Ryan P. Hillary,Smaranda Leu-Semenescu,Hanna Ollila,Hanna Ollila,Ling Lin,Eileen B. Leary,Andrea N. Goldstein-Piekarski,Yu-Shu Huang,Fang Han,Yakov Sivan,Michel Lecendreux,Pauline Dodet,Makoto Honda,Natan Gadoth,Sona Nevsimalova,Fabio Pizza,Takashi Kanbayashi,Rosa Peraita-Adrados,Guy D. Leschziner,Rosa Hasan,Francesca Canellas,Kazuhiko Kume,Makrina Daniilidou,Patrice Bourgin,David B. Rye,José L. Vicario,Birgit Högl,Seung Chul Hong,G. Plazzi,Geert Mayer,Anne Marie Landtblom,Yves Dauvilliers,Isabelle Arnulf,Emmanuel Mignot +34 more
TL;DR: In this paper, the TRANK1 rs71947865 polymorphisms were found to be associated with a higher risk of having a difficult birth in 673 Kleine-Levin Syndrome patients.
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