Showing 1–5 of 5 results
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Research | | Open
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
- C. S. Gallagher
- , N. Mäkinen
- , H. R. Harris
- , N. Rahmioglu
- , O. Uimari
- , J. P. Cook
- , N. Shigesi
- , T. Ferreira
- , D. R. Velez-Edwards
- , T. L. Edwards
- , S. Mortlock
- , Z. Ruhioglu
- , F. Day
- , C. M. Becker
- , V. Karhunen
- , H. Martikainen
- , M.-R. Järvelin
- , R. M. Cantor
- , P. M. Ridker
- , K. L. Terry
- , J. E. Buring
- , S. D. Gordon
- , S. E. Medland
- , G. W. Montgomery
- , D. R. Nyholt
- , D. A. Hinds
- , J. Y. Tung
- , Michelle Agee
- , Babak Alipanahi
- , Adam Auton
- , Robert K. Bell
- , Katarzyna Bryc
- , Sarah L. Elson
- , Pierre Fontanillas
- , Nicholas A. Furlotte
- , Karen E. Huber
- , Aaron Kleinman
- , Nadia K. Litterman
- , Matthew H. McIntyre
- , Joanna L. Mountain
- , Elizabeth S. Noblin
- , Carrie A. M. Northover
- , Steven J. Pitts
- , J. Fah Sathirapongsasuti
- , Olga V. Sazonova
- , Janie F. Shelton
- , Suyash Shringarpure
- , Chao Tian
- , Vladimir Vacic
- , Catherine H. Wilson
- , J. R. B. Perry
- , P. A. Lind
- , J. N. Painter
- , N. G. Martin
- , A. P. Morris
- , D. I. Chasman
- , S. A. Missmer
- , K. T. Zondervan
- & C. C. Morton
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Research |
LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells
- C Francks
- , S Maegawa
- , J Laurén
- , B S Abrahams
- , A Velayos-Baeza
- , S E Medland
- , S Colella
- , M Groszer
- , E Z McAuley
- , T M Caffrey
- , T Timmusk
- , P Pruunsild
- , I Koppel
- , P A Lind
- , N Matsumoto-Itaba
- , J Nicod
- , L Xiong
- , R Joober
- , W Enard
- , B Krinsky
- , E Nanba
- , A J Richardson
- , B P Riley
- , N G Martin
- , S M Strittmatter
- , H-J Möller
- , D Rujescu
- , D St Clair
- , P Muglia
- , J L Roos
- , S E Fisher
- , R Wade-Martins
- , G A Rouleau
- , J F Stein
- , M Karayiorgou
- , D H Geschwind
- , J Ragoussis
- , K S Kendler
- , M S Airaksinen
- , M Oshimura
- , L E DeLisi
- & A P Monaco
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Research |
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Research |
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Research |
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
- C Francks
- , S Maegawa
- , J Laurén
- , B S Abrahams
- , A Velayos-Baeza
- , S E Medland
- , S Colella
- , M Groszer
- , E Z McAuley
- , T M Caffrey
- , T Timmusk
- , P Pruunsild
- , I Koppel
- , P A Lind
- , N Matsumoto-Itaba
- , J Nicod
- , L Xiong
- , R Joober
- , W Enard
- , B Krinsky
- , E Nanba
- , A J Richardson
- , B P Riley
- , N G Martin
- , S M Strittmatter
- , H-J Möller
- , D Rujescu
- , D St Clair
- , P Muglia
- , J L Roos
- , S E Fisher
- , R Wade-Martins
- , G A Rouleau
- , J F Stein
- , M Karayiorgou
- , D H Geschwind
- , J Ragoussis
- , K S Kendler
- , M S Airaksinen
- , M Oshimura
- , L E DeLisi
- & A P Monaco
