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S

Struan F.A. Grant

children's hospital of philadelphia
H指数:96
被引数:4.4万

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荣誉奖项

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Trans-ancestry genome-wide association meta-analysis of gallstone disease

跨人群全基因组关联荟萃分析胆石病

Nature Communications
IF15.7
2026-10-220
OAAI
Junghyun Lim; Marijana Vujkovic; Michael G. Levin; Kim Lorenz; Benjamin F. Voight; David Y. Zhang; Max. F. Dudek; Matthew C. Pahl; James A. Pippin; Chun Su; Elisabetta Manduchi; Andrew D. Wells; Struan F. A. Grant; Sarah Abramowitz; Scott M. Damrauer; Samiran Mukherjee; Guoyi Yang; Lindsay Guare; Shefali Setia-Verma; David E. Kaplan; Daniel J. Rader
3D chromatin-based variant-to-gene maps across 57 human cell types reveal the cellular and genetic architecture of autoimmune disease susceptibility

基于3D染色质的变异-基因图谱在57种人类细胞类型中的研究揭示了自身免疫性疾病易感性的细胞和遗传架构

Genome Biology
IF9.4
2025-12-080
OAAI
Khanh B. Trang; Prabhat Sharma; Laura Cook; Zachary Mount; Rajan M. Thomas; Nikhil N. Kulkarni; Emylette Cruz Cabrera; Suzanna Rachimi; Matthew C. Pahl; James A. Pippin; Chun Su; Klaus H. Kaestner; Joan M. O’Brien; Yadav Wagley; Kurt D. Hankenson; Ashley Jermusyk; Jason W. Hoskins; Laufey T. Amundadottir; Mai Xu; Kevin M. Brown; Stewart A. Anderson; Wenli Yang; Paul M. Titchenell; Patrick Seale; Babette S. Zemel; Alessandra Chesi; Neil Romberg; Megan K. Levings; Struan F. A. Grant; Andrew D. Wells
GWAS-informed data integration and non-coding CRISPRi screen illuminate genetic etiology of bone mineral density

全基因组关联研究指导的数据整合与非编码CRISPRi筛选阐明骨密度的遗传病因

Genome Biology
IF9.4
2025-10-040
OAAI
Mitchell Conery; James A. Pippin; Yadav Wagley; Khanh Trang; Matthew C. Pahl; David A. Villani; Lacey J. Favazzo; Cheryl L. Ackert-Bicknell; Michael J. Zuscik; Eugene Katsevich; Andrew D. Wells; Babette S. Zemel; Benjamin F. Voight; Kurt D. Hankenson; Alessandra Chesi; Struan F. A. Grant
Mapping chromatin interactions at melanoma susceptibility loci uncovers distant cis-regulatory gene targets

绘制黑色素瘤易感位点的染色质相互作用图谱，揭示了远端顺式调控基因靶点

american journal of human genetics
IF0
2025-05-220
PRE
Rohit Thakur; Mai Xu; Hayley Sowards; Joshuah Yon; Lea Jessop; Timothy Myers; Tongwu Zhang; Raj Chari; Erping Long; Thomas Rehling; Rebecca Hennessey; Karen Funderburk; Jinhu Yin; Mitchell J. Machiela; Matthew E. Johnson; Andrew D. Wells; Alessandra Chesi; Struan F.A. Grant; Mark M. Iles; Maria Teresa Landi; Matthew H. Law; Jiyeon Choi; Kevin M. Brown
Trans-ancestry genome-wide association study of childhood body mass index identifies novel loci and age-specific effects
HUMAN GENETICS AND GENOMICS ADVANCES
IF3.6
2025-04-010
OAAI
Downie, Carolina G.; Shrestha, Poojan; Okello, Samson; Yaser, Mohammad; Lee, Harold H.; Wang, Yujie; Josyula, Navya Shilpa; Gahagan, Sheila; Burrows, Raquel; Correa-Burrows, Paulina; Albala, Cecilia; Santos, Jose L.; Angel, Barbara; Lozoff, Betsy; Blanco, Estela; Hartwig, Fernando Pires; Horta, Bernardo; Brina, Karisa Roxo; Isasi, Carmen R.; Qi, Qibin; Gallo, Linda C.; Perreira, Krista M.; Thyagarajan, Bharat; Daviglus, Martha; Van Horn, Linda; Chittoor, Geetha; Justice, Anne E.; Krishnan, Mohanraj; Chen, Hung-Hsin; Gonzalez, Franklyn; Bradfield, Jonathan P.; Hakonarson, Hakon; Grant, Struan F. A.; Below, Jennifer E.; Felix, Janine; Graff, Mariaelisa; Divaris, Kimon; North, Kari E.
3D genomic features across >50 diverse cell types reveal insights into the genomic architecture of childhood obesity
ELIFE
IF0
2025-01-150
OA
Trang, Khanh B.; Pahl, Matthew C.; Pippin, James A.; Su, Chun; Littleton, Sheridan H.; Sharma, Prabhat; Kulkarni, Nikhil N.; Ghanem, Louis R.; Terry, Natalie A.; O'Brien, Joan M.; Wagley, Yadav; Hankenson, Kurt D.; Jermusyk, Ashley; Hoskins, Jason; Amundadottir, Laufey T.; Xu, Mai; Brown, Kevin; Anderson, Stewart; Yang, Wenli; Titchenell, Paul; Seale, Patrick; Kaestner, Klaus H.; Cook, Laura; Levings, Megan; Zemel, Babette S.; Chesi, Alessandra; Wells, Andrew D.; Grant, Struan F. A.
Understanding the genetic complexity of puberty timing across the allele frequency spectrum

了解等位基因频谱中青春期时间的遗传复杂性

NATURE GENETICS
IF31.8
2024-07-013
OAAI
Kentistou, Katherine A.; Kaisinger, Lena R.; Stankovic, Stasa; Vaudel, Marc; de Oliveira, Edson Mendes; Messina, Andrea; Walters, Robin G.; Liu, Xiaoxi; Busch, Alexander S.; Helgason, Hannes; Thompson, Deborah J.; Santoni, Federico; Petricek, Konstantin M.; Zouaghi, Yassine; Huang-Doran, Isabel; Gudbjartsson, Daniel F.; Bratland, Eirik; Lin, Kuang; Gardner, Eugene J.; Zhao, Yajie; Jia, Raina Y.; Terao, Chikashi; Riggan, Marjorie J.; Bolla, Manjeet K.; Yazdanpanah, Mojgan; Yazdanpanah, Nahid; Bradfield, Jonathan P.; Broer, Linda; Campbell, Archie; Chasman, Daniel I.; Cousminer, Diana L.; Franceschini, Nora; Franke, Lude H.; Girotto, Giorgia; He, Chunyan; Jarvelin, Marjo-Riitta; Joshi, Peter K.; Kamatani, Yoichiro; Karlsson, Robert; Luan, Jian'an; Lunetta, Kathryn L.; Magi, Reedik; Mangino, Massimo; Medland, Sarah E.; Meisinger, Christa; Noordam, Raymond; Nutile, Teresa; Concas, Maria Pina; Polasek, Ozren; Porcu, Eleonora; Ring, Susan M.; Sala, Cinzia; Smith, Albert V.; Tanaka, Toshiko; Van der Most, Peter J.; Vitart, Veronique; Wang, Carol A.; Willemsen, Gonneke; Zygmunt, Marek; Ahearn, Thomas U.; Andrulis, Irene L.; Anton-Culver, Hoda; Antoniou, Antonis C.; Auer, Paul L.; Barnes, Catriona L. K.; Beckmann, Matthias W.; de Gonzalez, Amy Berrington; Bogdanova, Natalia V.; Bojesen, Stig E.; Brenner, Hermann; Buring, Julie E.; Canzian, Federico; Chang-Claude, Jenny; Couch, Fergus J.; Cox, Angela; Crisponi, Laura; Czene, Kamila; Daly, Mary B.; Demerath, Ellen W.; Dennis, Joe; Devilee, Peter; De Vivo, Immaculata; Doerk, Thilo; Dunning, Alison M.; Dwek, Miriam; Eriksson, Johan G.; Fasching, Peter A.; Fernandez-Rhodes, Lindsay; Ferreli, Liana; Fletcher, Olivia; Gago-Dominguez, Manuela; Garcia-Closas, Montserrat; Garcia-Saenz, Jose A.; Gonzalez-Neira, Anna; Grallert, Harald; Guenel, Pascal; Haiman, Christopher A.; Hall, Per; Hamann, Ute; Hakonarson, Hakon; Hart, Roger J.; Hickey, Martha; Hooning, Maartje J.; Hoppe, Reiner; Hopper, John L.; Hottenga, Jouke-Jan; Hu, Frank B.; Huebner, Hanna; Hunter, David J.; Jernstrom, Helena; John, Esther M.; Karasik, David; Khusnutdinova, Elza K.; Kristensen, Vessela N.; Lacey, James V.; Lambrechts, Diether; Launer, Lenore J.; Lind, Penelope A.; Lindblom, Annika; Magnusson, Patrik K. E.; Mannermaa, Arto; McCarthy, Mark I.; Meitinger, Thomas; Menni, Cristina; Michailidou, Kyriaki; Millwood, Iona Y.; Milne, Roger L.; Montgomery, Grant W.; Nevanlinna, Heli; Nolte, Ilja M.; Nyholt, Dale R.; Obi, Nadia; O'Brien, Katie M.; Offit, Kenneth; Oldehinkel, Albertine J.; Ostrowski, Sisse R.; Palotie, Aarno; Pedersen, Ole B.; Peters, Annette; Pianigiani, Giulia; Plaseska-Karanfilska, Dijana; Pouta, Anneli; Pozarickij, Alfred; Radice, Paolo; Rennert, Gad; Rosendaal, Frits R.; Ruggiero, Daniela; Saloustros, Emmanouil; Sandler, Dale P.; Schipf, Sabine; Schmidt, Carsten O.; Schmidt, Marjanka K.; Small, Kerrin; Spedicati, Beatrice; Stampfer, Meir; Stone, Jennifer; Tamimi, Rulla M.; Teras, Lauren R.; Tikkanen, Emmi; Turman, Constance; Vachon, Celine M.; Wang, Qin; Winqvist, Robert; Wolk, Alicja; Zemel, Babette S.; Zheng, Wei; van Dijk, Ko W.; Alizadeh, Behrooz Z.; Bandinelli, Stefania; Boerwinkle, Eric; Boomsma, Dorret I.; Ciullo, Marina; Chenevix-Trench, Georgia; Cucca, Francesco; Esko, Tonu; Gieger, Christian; Grant, Struan F. A.; Gudnason, Vilmundur; Hayward, Caroline; Kolcic, Ivana; Kraft, Peter; Lawlor, Deborah A.; Martin, Nicholas G.; Nohr, Ellen A.; Pedersen, Nancy L.; Pennell, Craig E.; Ridker, Paul M.; Robino, Antonietta; Snieder, Harold; Sovio, Ulla; Spector, Tim D.; Stockl, Doris; Sudlow, Cathie; Timpson, Nic J.; Toniolo, Daniela; Uitterlinden, Andre; Ulivi, Sheila; Volzke, Henry; Wareham, Nicholas J.; Widen, Elisabeth; Wilson, James F.; Pharoah, Paul D. P.; Li, Liming; Easton, Douglas F.; Njolstad, Pal R.; Sulem, Patrick; Murabito, Joanne M.; Murray, Anna; Manousaki, Despoina; Juul, Anders; Erikstrup, Christian; Stefansson, Kari; Horikoshi, Momoko; Chen, Zhengming; Farooqi, I. Sadaf; Pitteloud, Nelly; Johansson, Stefan; Day, Felix R.; Perry, John R. B.; Ong, Ken K.
Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3 0 UTR of FAIM2

儿童肥胖chr12q13基因座的变异型功能分析表明，rs7132908是FAIM2 3 0 UTR内的因果变异。

CELL GENOMICS
IF9
2024-05-013
OAAI
Littleton, Sheridan H.; Trang, Khanh B.; Volpe, Christina M.; Cook, Kieona; DeBruyne, Nicole; Maguire, Jean Ann; Weidekamp, Mary Ann; Hodge, Kenyaita M.; Boehm, Keith; Lu, Sumei; Chesi, Alessandra; Bradfield, Jonathan P.; Pippin, James A.; Anderson, Stewart A.; Wells, Andrew D.; Pahl, Matthew C.; Grant, Struan F. A.

研究方向

暂未获取到该数据
H
Håkon Håkonarson
H 指数:177论文数:1,492被引数:15.9万
J
Jonathan P. Bradfield
H 指数:70论文数:307被引数:2.4万
A
Alessandra Chesi
H 指数:42论文数:165被引数:1.2万
A
Andrew D. Wells
H 指数:59论文数:320被引数:1.7万
J
Joseph Glessner
H 指数:76论文数:306被引数:3.0万
B
Babette S. Zemel
H 指数:90论文数:597被引数:2.8万
D
Diana L. Cousminer
H 指数:22论文数:62被引数:1,809
E
Edward C. Frackelton
H 指数:42论文数:86被引数:1.0万
R
Rosetta Chiavacci
H 指数:54论文数:144被引数:1.6万
M
Mark I. McCarthy
H 指数:222论文数:1,509被引数:26.6万