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Models to infer evolution in declining populations and across space

推断人口减少和跨空间进化的模型

基本信息

批准号：
DGECR-2021-00114
负责人：
Osmond, Matthew
金额：
$ 0.91万
依托单位：
University of Toronto
依托单位国家：
加拿大
项目类别：
Discovery Launch Supplement
财政年份：
2021
资助国家：
加拿大
起止时间：
2021-01-01 至 2022-12-31
项目状态：
已结题

来源：
https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=731803
关键词：
Models infer evolution declining populations

项目摘要

No summary - Aucun sommaire

没有摘要--Aucun Sommaire

项目成果

期刊论文数量（0）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

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Osmond, Matthew其他文献

Rare diseases and space health: optimizing synergies from scientific questions to care.

DOI：
10.1038/s41526-022-00224-5
发表时间：
2022-12-22
期刊：
NPJ MICROGRAVITY
影响因子：
5.1
作者：
Puscas, Maria;Martineau, Gabrielle;Bhella, Gurjot;Bonnen, Penelope E.;Carr, Phil;Lim, Robyn;Mitchell, John;Osmond, Matthew;Urquieta, Emmanuel;Flamenbaum, Jaime;Iaria, Giuseppe;Joly, Yann;Richer, Etienne;Saary, Joan;Saint-Jacques, David;Buckley, Nicole;Low-Decarie, Etienne
通讯作者：
Low-Decarie, Etienne

Outcome of over 1500 matches through the Matchmaker Exchange for rare disease gene discovery: The 2-year experience of Care4Rare Canada

DOI：
10.1016/j.gim.2021.08.014
发表时间：
2022-01-05
期刊：
GENETICS IN MEDICINE
影响因子：
8.8
作者：
Osmond, Matthew;Hartley, Taila;Boycott, Kym M.
通讯作者：
Boycott, Kym M.

Biallelic Variants in the Ectonucleotidase ENTPD1 Cause a Complex Neurodevelopmental Disorder with Intellectual Disability, Distinct White Matter Abnormalities, and Spastic Paraplegia.

DOI：
10.1002/ana.26381
发表时间：
2022-08
期刊：
ANNALS OF NEUROLOGY
影响因子：
11.2
作者：
Calame, Daniel G.;Herman, Isabella;Maroofian, Reza;Marshall, Aren E.;Donis, Karina Carvalho;Fatih, Jawid M.;Mitani, Tadahiro;Du, Haowei;Grochowski, Christopher M.;Sousa, Sergio B.;Gijavanekar, Charul;Bakhtiari, Somayeh;Ito, Yoko A.;Rocca, Clarissa;Hunter, Jill, V;Sutton, V. Reid;Emrick, Lisa T.;Boycott, Kym M.;Lossos, Alexander;Fellig, Yakov;Prus, Eugenia;Kalish, Yosef;Meiner, Vardiella;Suerink, Manon;Ruivenkamp, Claudia;Muirhead, Kayla;Saadi, Nebal W.;Zaki, Maha S.;Bouman, Arjan;Barakat, Tahsin Stefan;Skidmore, David L.;Osmond, Matthew;Silva, Thiago Oliveira;Murphy, David;Karimiani, Ehsan Ghayoor;Jamshidi, Yalda;Jaddoa, Asaad Ghanim;Tajsharghi, Homa;Jin, Sheng Chih;Abbaszadegan, Mohammad Reza;Ebrahimzadeh-Vesal, Reza;Hosseini, Susan;Alavi, Shahryar;Bahreini, Amir;Zarean, Elahe;Salehi, Mohammad Mehdi;Al-Sannaa, Nouriya Abbas;Zifarelli, Giovanni;Bauer, Peter;Robson, Simon C.;Coban-Akdemir, Zeynep;Travaglini, Lorena;Nicita, Francesco;Jhangiani, Shalini N.;Gibbs, Richard A.;Posey, Jennifer E.;Kruer, Michael C.;Kernohan, Kristin D.;Morales Saute, Jonas A.;Houlden, Henry;Vanderver, Adeline;Elsea, Sarah H.;Pehlivan, Davut;Marafi, Dana;Lupski, James R.
通讯作者：
Lupski, James R.

Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.

DOI：
10.1172/jci171235
发表时间：
2024-01-02
期刊：
JOURNAL OF CLINICAL INVESTIGATION
影响因子：
15.9
作者：
Li, Dong;Wang, Qin;Bayat, Allan;Battig, Mark R.;Zhou, Yijing;Bosch, Danielle G. M.;van Haaften, Gijs;Granger, Leslie;Petersen, Andrea K.;Perez-Jurado, Luis A.;Aznar-Lain, Gemma;Aneja, Anushree;Hancarova, Miroslava;Bendova, Sarka;Schwarz, Martin;Pourova, Radka Kremlikova;Sedlacek, Zdenek;Keena, Beth A.;March, Michael E.;Hou, Cuiping;O'Connor, Nora;Bhoj, Elizabeth J.;Harr, Margaret H.;Lemire, Gabrielle;Boycott, Kym M.;Towne, Meghan;Li, Megan;Tarnopolsky, Mark;Brady, Lauren;Parker, Michael J.;Faghfoury, Hanna;Parsley, Lea Kristin;Agolini, Emanuele;Dentici, Maria Lisa;Novelli, Antonio;Wright, Meredith;Palmquist, Rachel;Lai, Khanh;Scala, Marcello;Striano, Pasquale;Iacomino, Michele;Zara, Federico;Cooper, Annina;Maarup, Timothy J.;Byler, Melissa;Lebel, Robert Roger;Balci, Tugce B.;Louie, Raymond;Lyons, Michael;Douglas, Jessica;Nowak, Catherine;Afenjar, Alexandra;Hoyer, Juliane;Keren, Boris;Maas, Saskia M.;Motazacker, Mahdi M.;Martinez-Agosto, Julian A.;Rabani, Ahna M.;McCormick, Elizabeth M.;Falk, Marni J.;Ruggiero, Sarah M.;Helbig, Ingo;Moller, Rikke S.;Tessarollo, Lino;Ardori, Francesco Tomassoni;Palko, Mary Ellen;Hsieh, Tzung-Chien;Krawitz, Peter M.;Ganapathi, Mythily;Gelb, Bruce D.;Jobanputra, Vaidehi;Wilson, Ashley;Greally, John;Jacquemont, Sebastien;Jizi, Khadije;Bruel, Ange-Line;Quelin, Chloe;Misra, Vinod K.;Chick, Erika;Romano, Corrado;Greco, Donatella;Arena, Alessia;Morleo, Manuela;Nigro, Vincenzo;Seyama, Rie;Uchiyama, Yuri;Matsumoto, Naomichi;Taira, Ryoji;Tashiro, Katsuya;Sakai, Yasunari;Yigit, Gokhan;Wollnik, Bernd;Wagner, Michael;Kutsche, Barbara;Hurst, Anna C. E.;Thompson, Michelle L.;Schmidt, Ryan;Randolph, Linda;Spillmann, Rebecca C.;Shashi, Vandana;Higginbotham, Edward J.;Cordeiro, Dawn;Carnevale, Amanda;Costain, Gregory;Khan, Tayyaba;Funalot, Benoit;Mau-Them, Frederic Tran;Moya, Luis Fernandez Garcia;Garcia-Minaur, Sixto;Osmond, Matthew;Chad, Lauren;Quercia, Nada;Carrasco, Diana;Li, Chumei;Sanchez-Valle, Amarilis;Kelley, Meghan;Nizon, Mathilde;Jensson, Brynjar O.;Sulem, Patrick;Stefansson, Kari;Gorokhova, Svetlana;Busa, Tiffany;Rio, Marlene;Habdallah, Hamza Hadj;Lesieur-Sebellin, Marion;Amiel, Jeanne;Pingault, Veronique;Mercier, Sandra;Vincent, Marie;Philippe, Christophe;Fatus-Fauconnier, Clemence;Friend, Kathryn;Halligan, Rebecca K.;Biswas, Sunita;Rosser, Jane;Shoubridge, Cheryl;Corbett, Mark;Barnett, Christopher;Gecz, Jozef;Leppig, Kathleen;Slavotinek, Anne;Marcelis, Carlo;Pfundt, Rolph;de Vries, Bert B. A.;van Slegtenhorst, Marjon A.;Brooks, Alice S.;Cogne, Benjamin;Rambaud, Thomas;Tumer, Zeynep;Zackai, Elaine H.;Akizu, Naiara;Song, Yuanquan;Hakonarson, Hakon
通讯作者：
Hakonarson, Hakon