Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 442 Records) |
Query Trace: CAMP[original query] |
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A pleiotropic variant in DNAJB4 is associated with multiple myeloma risk. International journal of cancer 2022 9 152 (2): 239-248. Dicanio Marco, Giaccherini Matteo, Clay-Gilmour Alyssa, Macauda Angelica, Sainz Juan, Machiela Mitchell J, Rybicka-Ramos Malwina, Norman Aaron D, Tyczy?ska Agata, Chanock Stephen J, Barington Torben, Kumar Shaji K, Bhatti Parveen, Cozen Wendy, Brown Elizabeth E, Suska Anna, Haastrup Eva K, Orlowski Robert Z, Dudzi?ski Marek, Garcia-Sanz Ramon, Kruszewski Marcin, Martinez-Lopez Joaquin, Beider Katia, Iskierka-Jazdzewska El?bieta, Pelosini Matteo, Berndt Sonja I, Ra?ny Ma?gorzata, Jamroziak Krzysztof, Rajkumar S Vincent, Jurczyszyn Artur, Vangsted Annette Juul, Collado Pilar Garrido, Vogel Ulla, Hofmann Jonathan N, Petrini Mario, Butrym Aleksandra, Slager Susan L, Ziv Elad, Subocz Edyta, Giles Graham G, Andersen Niels Frost, Mazur Grzegorz, Watek Marzena, Lesueur Fabienne, Hildebrandt Michelle A T, Zawirska Daria, Ebbesen Lene Hyldahl, Marques Herlander, Gemignani Federica, Dumontet Charles, Várkonyi Judit, Buda Gabriele, Nagler Arnon, Druzd-Sitek Agnieszka, Wu Xifeng, Kadar Katalin, Camp Nicola J, Grzasko Norbert, Waller Rosalie G, Vachon Celine, Canzian Federico, Campa Danie |
Genetic regulation of RNA splicing in human pancreatic islets. Genome biology 2022 9 23 (1): 196. Atla Goutham, Bonàs-Guarch Silvia, Cuenca-Ardura Mirabai, Beucher Anthony, Crouch Daniel J M, Garcia-Hurtado Javier, Moran Ignasi, , Irimia Manuel, Prasad Rashmi B, Gloyn Anna L, Marselli Lorella, Suleiman Mara, Berney Thierry, de Koning Eelco J P, Kerr-Conte Julie, Pattou Francois, Todd John A, Piemonti Lorenzo, Ferrer Jor |
DDX58 Is Associated With Susceptibility to Severe Influenza Virus Infection in Children and Adolescents. The Journal of infectious diseases 2022 Aug . Lee Sanghun, Zhang Yu, Newhams Margaret, Novak Tanya, Thomas Paul G, Mourani Peter M, Hall Mark W, Loftis Laura L, Cvijanovich Natalie Z, Tarquinio Keiko M, Schwarz Adam J, Weiss Scott L, Thomas Neal J, Markovitz Barry, Cullimore Melissa L, Sanders Ronald C, Zinter Matt S, Sullivan Janice E, Halasa Natasha B, Bembea Melania M, Giuliano John S, Typpo Katri V, Nofziger Ryan A, Shein Steven L, Kong Michele, Coates Bria M, Weiss Scott T, Lange Christoph, Su Helen C, Randolph Adrienne G, |
Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study. Journal of clinical medicine 2022 12 11 (23): . Tavernier Lisse J M, Vanpoucke Thomas, Schrauwen Isabelle, Van Camp Guy, Fransen Er |
Synapsin III Regulates Dopaminergic Neuron Development in Vertebrates. Cells 2022 12 11 (23): . Faustini Gaia, Longhena Francesca, Muscò Alessia, Bono Federica, Parrella Edoardo, La Via Luca, Barbon Alessandro, Pizzi Marina, Onofri Franco, Benfenati Fabio, Missale Cristina, Memo Maurizio, Zizioli Daniela, Bellucci Arian |
Physical activity, sedentary time and breast cancer risk: a Mendelian randomisation study. British journal of sports medicine 2022 11 56 (20): 1157-1170. Dixon-Suen Suzanne C, Lewis Sarah J, Martin Richard M, English Dallas R, Boyle Terry, Giles Graham G, Michailidou Kyriaki, Bolla Manjeet K, Wang Qin, Dennis Joe, Lush Michael, Investigators Abctb, Ahearn Thomas U, Ambrosone Christine B, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Aronson Kristan J, Augustinsson Annelie, Auvinen Päivi, Beane Freeman Laura E, Becher Heiko, Beckmann Matthias W, Behrens Sabine, Bermisheva Marina, Blomqvist Carl, Bogdanova Natalia V, Bojesen Stig E, Bonanni Bernardo, Brenner Hermann, Brüning Thomas, Buys Saundra S, Camp Nicola J, Campa Daniele, Canzian Federico, Castelao Jose E, Cessna Melissa H, Chang-Claude Jenny, Chanock Stephen J, Clarke Christine L, Conroy Don M, Couch Fergus J, Cox Angela, Cross Simon S, Czene Kamila, Daly Mary B, Devilee Peter, Dörk Thilo, Dwek Miriam, Eccles Diana M, Eliassen A Heather, Engel Christoph, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Fletcher Olivia, Flyger Henrik, Fritschi Lin, Gabrielson Marike, Gago-Dominguez Manuela, García-Closas Montserrat, García-Sáenz José A, Goldberg Mark S, Guénel Pascal, Gündert Melanie, Hahnen Eric, Haiman Christopher A, Häberle Lothar, Håkansson Niclas, Hall Per, Hamann Ute, Hart Steven N, Harvie Michelle, Hillemanns Peter, Hollestelle Antoinette, Hooning Maartje J, Hoppe Reiner, Hopper John, Howell Anthony, Hunter David J, Jakubowska Anna, Janni Wolfgang, John Esther M, Jung Audrey, Kaaks Rudolf, Keeman Renske, Kitahara Cari M, Koutros Stella, Kraft Peter, Kristensen Vessela N, Kubelka-Sabit Katerina, Kurian Allison W, Lacey James V, Lambrechts Diether, Le Marchand Loic, Lindblom Annika, Loibl Sibylle, Lubi?ski Jan, Mannermaa Arto, Manoochehri Mehdi, Margolin Sara, Martinez Maria Elena, Mavroudis Dimitrios, Menon Usha, Mulligan Anna Marie, Murphy Rachel A, Collaborators Nbcs, Nevanlinna Heli, Nevelsteen Ines, Newman William G, Offit Kenneth, Olshan Andrew F, Olsson Håkan, Orr Nick, Patel Alpa, Peto Julian, Plaseska-Karanfilska Dijana, Presneau Nadege, Rack Brigitte, Radice Paolo, Rees-Punia Erika, Rennert Gad, Rennert Hedy S, Romero Atocha, Saloustros Emmanouil, Sandler Dale P, Schmidt Marjanka K, Schmutzler Rita K, Schwentner Lukas, Scott Christopher, Shah Mitul, Shu Xiao-Ou, Simard Jacques, Southey Melissa C, Stone Jennifer, Surowy Harald, Swerdlow Anthony J, Tamimi Rulla M, Tapper William J, Taylor Jack A, Terry Mary Beth, Tollenaar Rob A E M, Troester Melissa A, Truong Thérèse, Untch Michael, Vachon Celine M, Joseph Vijai, Wappenschmidt Barbara, Weinberg Clarice R, Wolk Alicja, Yannoukakos Drakoulis, Zheng Wei, Ziogas Argyrios, Dunning Alison M, Pharoah Paul D P, Easton Douglas F, Milne Roger L, Lynch Brigid M, |
Association of PPP1R1B polymorphisms with working memory in healthy Han Chinese adults. Frontiers in neuroscience 2022 11 16 989046. Ma Hui, Qiu Riyang, Zhang Wenya, Chen Xiaohong, Zhang Liguo, Wang M |
CC Genotype of GNAS c.393C>T (rs7121) Polymorphism Has a Protective Effect against Development of BK Viremia and BKV-Associated Nephropathy after Renal Transplant. Pathogens (Basel, Switzerland) 2022 10 11 (10): . Peitz Tobias, Möhlendick Birte, Eisenberger Ute, Siffert Winfried, Heinemann Falko Markus, Kribben Andreas, Friebus-Kardash Jus |
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes.
Leukemia 2022 Oct . Berndt Sonja I, Vijai Joseph, Benavente Yolanda, Camp Nicola J, Nieters Alexandra, Wang Zhaoming, Smedby Karin E, Kleinstern Geffen, Hjalgrim Henrik, Besson Caroline, Skibola Christine F, Morton Lindsay M, Brooks-Wilson Angela R, Teras Lauren R, Breeze Charles, Arias Joshua, Adami Hans-Olov, Albanes Demetrius, Anderson Kenneth C, Ansell Stephen M, Bassig Bryan, Becker Nikolaus, Bhatti Parveen, Birmann Brenda M, Boffetta Paolo, Bracci Paige M, Brennan Paul, Brown Elizabeth E, Burdett Laurie, Cannon-Albright Lisa A, Chang Ellen T, Chiu Brian C H, Chung Charles C, Clavel Jacqueline, Cocco Pierluigi, Colditz Graham, Conde Lucia, Conti David V, Cox David G, Curtin Karen, Casabonne Delphine, De Vivo Immaculata, Diver W Ryan, Dogan Ahmet, Edlund Christopher K, Foretova Lenka, Fraumeni Joseph F, Gabbas Attilio, Ghesquières Hervé, Giles Graham G, Glaser Sally, Glenn Martha, Glimelius Bengt, Gu Jian, Habermann Thomas M, Haiman Christopher A, Haioun Corinne, Hofmann Jonathan N, Holford Theodore R, Holly Elizabeth A, Hutchinson Amy, Izhar Aalin, Jackson Rebecca D, Jarrett Ruth F, Kaaks Rudolph, Kane Eleanor, Kolonel Laurence N, Kong Yinfei, Kraft Peter, Kricker Anne, Lake Annette, Lan Qing, Lawrence Charles, Li Dalin, Liebow Mark, Link Brian K, Magnani Corrado, Maynadie Marc, McKay James, Melbye Mads, Miligi Lucia, Milne Roger L, Molina Thierry J, Monnereau Alain, Montalvan Rebecca, North Kari E, Novak Anne J, Onel Kenan, Purdue Mark P, Rand Kristin A, Riboli Elio, Riby Jacques, Roman Eve, Salles Gilles, Sborov Douglas W, Severson Richard K, Shanafelt Tait D, Smith Martyn T, Smith Alexandra, Song Kevin W, Song Lei, Southey Melissa C, Spinelli John J, Staines Anthony, Stephens Deborah, Sutherland Heather J, Tkachuk Kaitlyn, Thompson Carrie A, Tilly Hervé, Tinker Lesley F, Travis Ruth C, Turner Jenny, Vachon Celine M, Vajdic Claire M, Van Den Berg Anke, Van Den Berg David J, Vermeulen Roel C H, Vineis Paolo, Wang Sophia S, Weiderpass Elisabete, Weiner George J, Weinstein Stephanie, Doo Nicole Wong, Ye Yuanqing, Yeager Meredith, Yu Kai, Zeleniuch-Jacquotte Anne, Zhang Yawei, Zheng Tongzhang, Ziv Elad, Sampson Joshua, Chatterjee Nilanjan, Offit Kenneth, Cozen Wendy, Wu Xifeng, Cerhan James R, Chanock Stephen J, Slager Susan L, Rothman Nathani |
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~?200,000 patients. Breast cancer research : BCR 2022 10 24 (1): 69. Giardiello Daniele, Hooning Maartje J, Hauptmann Michael, Keeman Renske, Heemskerk-Gerritsen B A M, Becher Heiko, Blomqvist Carl, Bojesen Stig E, Bolla Manjeet K, Camp Nicola J, Czene Kamila, Devilee Peter, Eccles Diana M, Fasching Peter A, Figueroa Jonine D, Flyger Henrik, García-Closas Montserrat, Haiman Christopher A, Hamann Ute, Hopper John L, Jakubowska Anna, Leeuwen Floor E, Lindblom Annika, Lubi?ski Jan, Margolin Sara, Martinez Maria Elena, Nevanlinna Heli, Nevelsteen Ines, Pelders Saskia, Pharoah Paul D P, Siesling Sabine, Southey Melissa C, van der Hout Annemieke H, van Hest Liselotte P, Chang-Claude Jenny, Hall Per, Easton Douglas F, Steyerberg Ewout W, Schmidt Marjanka |
Interplay of Mendelian and polygenic risk factors in Arab breast cancer patients. Genome medicine 2023 9 15 (1): 65. Mohammed Al-Jumaan, Hoyin Chu, Abdullah Alsulaiman, Sabrina Y Camp, Seunghun Han, Riaz Gillani, Yousef Al Marzooq, Fatmah Almulhim, Chittibabu Vatte, Areej Al Nemer, Afnan Almuhanna, Eliezer M Van Allen, Amein Al-Ali, Saud H AlDubay |
Carriers of rare damaging CCR2 genetic variants are at lower risk of atherosclerotic disease. medRxiv : the preprint server for health sciences 2023 8 . Marios K Georgakis, Rainer Malik, Natalie R Hasbani, Gabrielle Shakt, Alanna C Morrison, Noah L Tsao, Renae Judy, Braxton D Mitchell, Huichun Xu, May E Montasser, Ron Do, Eimear E Kenny, Ruth J F Loos, James G Terry, John Jeffrey Carr, Joshua C Bis, Bruce M Psaty, W T Longstreth, Kendra A Young, Sharon M Lutz, Michael H Cho, Jai Broome, Alyna T Khan, Fei Fei Wang, Nancy Heard-Costa, Sudha Seshadri, Ramachandran S Vasan, Nicholette D Palmer, Barry I Freedman, Donald W Bowden, Lisa R Yanek, Brian G Kral, Lewis C Becker, Patricia A Peyser, Lawrence F Bielak, Farah Ammous, April P Carson, Michael E Hall, Laura M Raffield, Stephen S Rich, Wendy S Post, Russel P Tracy, Kent D Taylor, Xiuqing Guo, Michael C Mahaney, Joanne E Curran, John Blangero, Shoa L Clarke, Jeffrey W Haessler, Yao Hu, Themistocles L Assimes, Charles Kooperberg, Scott M Damrauer, Jerome I Rotter, Paul S de Vries, Martin Dichga |
Noncoding SNP at rs1663689 represses ADGRG6 via interchromosomal interaction and reduces lung cancer progression. EMBO reports 2023 5 e56212. Xinyue Lei, Xiaoling Tian, Hao Wang, Xinran Xu, Guoli Li, Wenxu Liu, Dan Wang, Zengtuan Xiao, Mengzhe Zhang, Mulin Jun Li, Zhenfa Zhang, Zhenyi Ma, Zhe L |
Polymorphisms within Autophagy-Related Genes as Susceptibility Biomarkers for Multiple Myeloma: A Meta-Analysis of Three Large Cohorts and Functional Characterization. International journal of molecular sciences 2023 5 24 (10): . Esther Clavero, José Manuel Sanchez-Maldonado, Angelica Macauda, Rob Ter Horst, Belém Sampaio-Marques, Artur Jurczyszyn, Alyssa Clay-Gilmour, Angelika Stein, Michelle A T Hildebrandt, Niels Weinhold, Gabriele Buda, Ramón García-Sanz, Waldemar Tomczak, Ulla Vogel, Andrés Jerez, Daria Zawirska, Marzena W?tek, Jonathan N Hofmann, Stefano Landi, John J Spinelli, Aleksandra Butrym, Abhishek Kumar, Joaquín Martínez-López, Sara Galimberti, María Eugenia Sarasquete, Edyta Subocz, Elzbieta Iskierka-Ja?d?ewska, Graham G Giles, Malwina Rybicka-Ramos, Marcin Kruszewski, Niels Abildgaard, Francisco García Verdejo, Pedro Sánchez Rovira, Miguel Inacio da Silva Filho, Katalin Kadar, Ma?gorzata Razny, Wendy Cozen, Matteo Pelosini, Manuel Jurado, Parveen Bhatti, Marek Dudzinski, Agnieszka Druzd-Sitek, Enrico Orciuolo, Yang Li, Aaron D Norman, Jan Maciej Zaucha, Rui Manuel Reis, Miroslaw Markiewicz, Juan José Rodríguez Sevilla, Vibeke Andersen, Krzysztof Jamroziak, Kari Hemminki, Sonja I Berndt, Vicent Rajkumar, Grzegorz Mazur, Shaji K Kumar, Paula Ludovico, Arnon Nagler, Stephen J Chanock, Charles Dumontet, Mitchell J Machiela, Judit Varkonyi, Nicola J Camp, Elad Ziv, Annette Juul Vangsted, Elizabeth E Brown, Daniele Campa, Celine M Vachon, Mihai G Netea, Federico Canzian, Asta Försti, Juan Sai |
Rare heterozygous loss-of-function variants in the human GLP-1 receptor do not associate with cardiometabolic phenotypes. The Journal of clinical endocrinology and metabolism 2023 5 . Josefine U Melchiorsen, Kimmie V Sørensen, Jette Bork-Jensen, Hüsün S Kizilkaya, Lærke S Gasbjerg, Alexander S Hauser, Jørgen Rungby, Henrik T Sørensen, Allan Vaag, Jens S Nielsen, Oluf Pedersen, Allan Linneberg, Bolette Hartmann, Anette P Gjesing, Jens J Holst, Torben Hansen, Mette M Rosenkilde, Niels Grar |
A Belgian Population-Based Study Reveals Subgroups of Right-Sided Colorectal Cancer with a Better Prognosis Compared to Left-sided Cancer. The oncologist 0 . Janssens Katleen, Fransen Erik, Van Camp Guy, Prenen Hans, Op de Beeck Ken, Van Damme Nancy, Peeters Ma |
Identification of single nucleotide variants in SLC26A9 gene in patients with cystic fibrosis (p.Phe508del homozygous) and its association to Orkambi® (Lumacaftor and Ivacaftor) response in vitro. Gene 2023 4 871 147428. Santos Luana Gavioli, Pereira Stéphanie Villa-Nova, Kmit Arthur Henrique Pezzo, Bonadia Luciana Cardoso, Bertuzzo Carmen Sílvia, Ribeiro José Dirceu, Mazzola Taís Nitsch, Marson Fernando Augusto Li |
Overcoming barriers to tumor genomic profiling through direct-to-patient outreach. Clinical cancer research : an official journal of the American Association for Cancer Research 2023 3 . Doe-Tetteh Seyram A, Camp Sabrina Y, Reales Dalicia, Crowdis Jett, Noronha Anne Marie, Wolff Bernadette, Alano Tina, Galle Jesse, Selcuklu S Duygu, Viale Agnes, Socci Nicholas D, Liu Ying L, Tew William P, Aghajanian Carol, Ladanyi Marc, He Meng Xiao, AlDubayan Saud H, Mazor Roei David, Shpilberg Ofer, Hershkovitz-Rokah Oshrat, Riancho Jose A, Hernandez Jose L, Gonzalez-Vela M Carmen, Buthorn Justin J, Wilson Manda, Webber Amy E, Yabe Mariko, Petrova-Drus Kseniya, Rosenblum Marc, Durham Benjamin H, Abdel-Wahab Omar, Berger Michael F, Donoghue Mark T A, Kung Andrew L, Glade Bender Julia, Shukla Neerav N, Funt Samuel A, Dogan Ahmet, Soslow Robert A, Al-Ahmadie Hikmat, Feldman Darren R, Van Allen Eliezer M, Diamond Eli L, Solit David |
The impact of coding germline variants on contralateral breast cancer risk and survival. American journal of human genetics 2023 2 110 (3): 475-486. Morra Anna, Mavaddat Nasim, Muranen Taru A, Ahearn Thomas U, Allen Jamie, Andrulis Irene L, Auvinen Päivi, Becher Heiko, Behrens Sabine, Blomqvist Carl, Bojesen Stig E, Bolla Manjeet K, Brauch Hiltrud, Camp Nicola J, Carvalho Sara, Castelao Jose E, Cessna Melissa H, Chang-Claude Jenny, Chenevix-Trench Georgia, , Czene Kamila, Decker Brennan, Dennis Joe, Dörk Thilo, Dorling Leila, Dunning Alison M, Ekici Arif B, Eriksson Mikael, Evans D Gareth, Fasching Peter A, Figueroa Jonine D, Flyger Henrik, Gago-Dominguez Manuela, García-Closas Montserrat, Geurts-Giele Willemina R R, Giles Graham G, Guénel Pascal, Gündert Melanie, Hahnen Eric, Hall Per, Hamann Ute, Harrington Patricia A, He Wei, Heikkilä Päivi, Hooning Maartje J, Hoppe Reiner, Howell Anthony, Humphreys Keith, , Jakubowska Anna, Jung Audrey Y, Keeman Renske, Kristensen Vessela N, Lubi?ski Jan, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Mavroudis Dimitrios, Milne Roger L, Mulligan Anna Marie, Newman William G, Park-Simon Tjoung-Won, Peterlongo Paolo, Pharoah Paul D P, Rhenius Valerie, Saloustros Emmanouil, Sawyer Elinor J, Schmutzler Rita K, Shah Mitul, Spurdle Amanda B, Tomlinson Ian, Truong Thérèse, van Veen Elke M, Vreeswijk Maaike P G, Wang Qin, Wendt Camilla, Yang Xiaohong R, Nevanlinna Heli, Devilee Peter, Easton Douglas F, Schmidt Marjanka |
KLKB1 and CLSTN2 are associated with HDL-mediated cholesterol efflux capacity in a genome-wide association study. Atherosclerosis 2023 2 368 1-11. Schachtl-Riess Johanna F, Schönherr Sebastian, Lamina Claudia, Forer Lukas, Coassin Stefan, Streiter Gertraud, Kheirkhah Azin, Li Yong, Meiselbach Heike, Di Maio Silvia, Eckardt Kai-Uwe, Köttgen Anna, Kronenberg Florian, |
High-frequency variants in PKA signaling-related genes within a large pediatric cohort with obesity or metabolic abnormalities. Frontiers in endocrinology 2023 11 14 1272939. Michelle Bloyd, Ninet Sinaii, Fabio Rueda Faucz, James Iben, Steven L Coon, Sonia Caprio, Nicola Santoro, Constantine A Stratakis, Edra Lond |
First report on female monozygotic twins discordant for congenital nephrogenic diabetes insipidus. American journal of medical genetics. Part A 2023 11 . Xiang Chen, Libing Yun, Yang Long, Yuxia Sun, Tao Ch |
NOTCH1 and CREBBP co-mutations negatively affect the benefit of adjuvant therapy in completely resected EGFR-mutated NSCLC: translational research of phase III IMPACT study. Molecular oncology 2023 10 . Satoshi Ikeda, Masahiro Tsuboi, Kazuko Sakai, Toshihiro Misumi, Hiroaki Akamatsu, Hiroyasu Shoda, Noriaki Sakakura, Atsushi Nakamura, Yasuhisa Ohde, Hidetoshi Hayashi, Kyoichi Okishio, Morihito Okada, Ichiro Yoshino, Jiro Okami, Kazuhisa Takahashi, Norihiko Ikeda, Masayuki Tanahashi, Yuichi Tambo, Haruhiro Saito, Shinichi Toyooka, Hidetoshi Inokawa, Toyofumi Chen-Yoshikawa, Toshihide Yokoyama, Tatsuro Okamoto, Noriko Yanagitani, Masahide Oki, Makoto Takahama, Kenji Sawa, Hirohito Tada, Kazuhiko Nakagawa, Tetsuya Mitsudomi, Kazuto Nish |
Defective monocyte plasticity and altered cAMP pathway characterize USB1-mutated poikiloderma with neutropenia Clericuzio type. British journal of haematology 2023 10 . Prahlad Parajuli, Douglas B Craig, Manisha Gadgeel, Shruti Bagla, Robert E Wright, Roland Chu, Christina M Shanti, Rajeev Thirunagari, Sudershan K Grover, Yaddanapudi Ravindrana |
Integrative Analysis of Germline Rare Variants in Clear and Non-Clear Cell Renal Cell Carcinoma. medRxiv : the preprint server for health sciences 2023 1 . Han Seunghun, Camp Sabrina Y, Chu Hoyin, Collins Ryan, Gillani Riaz, Park Jihye, Bakouny Ziad, Ricker Cora A, Reardon Brendan, Moore Nicholas, Kofman Eric, Labaki Chris, Braun David, Choueiri Toni K, AlDubayan Saud H, Van Allen Eliezer |
Correlation between variants of the CREB1 and GRM7 genes and risk of depression. BMC psychiatry 2023 1 23 (1): 3. Wang Li, Tang Xingming, Liang Peng, Zhou Chuan, Sun Yingjie, Liang Yund |
FANCM missense variants and breast cancer risk: a case-control association study of 75,156 European women. European journal of human genetics : EJHG 2023 1 . Figlioli Gisella, Billaud Amandine, Ahearn Thomas U, Antonenkova Natalia N, Becher Heiko, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Blok Marinus J, Bogdanova Natalia V, Bonanni Bernardo, Burwinkel Barbara, Camp Nicola J, Campbell Archie, Castelao Jose E, Cessna Melissa H, Chanock Stephen J, , Czene Kamila, Devilee Peter, Dörk Thilo, Engel Christoph, Eriksson Mikael, Fasching Peter A, Figueroa Jonine D, Gabrielson Marike, Gago-Dominguez Manuela, García-Closas Montserrat, González-Neira Anna, Grassmann Felix, Guénel Pascal, Gündert Melanie, Hadjisavvas Andreas, Hahnen Eric, Hall Per, Hamann Ute, Harrington Patricia A, He Wei, Hillemanns Peter, Hollestelle Antoinette, Hooning Maartje J, Hoppe Reiner, Howell Anthony, Humphreys Keith, , Jager Agnes, Jakubowska Anna, Khusnutdinova Elza K, Ko Yon-Dschun, Kristensen Vessela N, Lindblom Annika, Lissowska Jolanta, Lubi?ski Jan, Mannermaa Arto, Manoukian Siranoush, Margolin Sara, Mavroudis Dimitrios, Newman William G, Obi Nadia, Panayiotidis Mihalis I, Rashid Muhammad U, Rhenius Valerie, Rookus Matti A, Saloustros Emmanouil, Sawyer Elinor J, Schmutzler Rita K, Shah Mitul, Sironen Reijo, Southey Melissa C, Suvanto Maija, Tollenaar Rob A E M, Tomlinson Ian, Truong Thérèse, van der Kolk Lizet E, van Veen Elke M, Wappenschmidt Barbara, Yang Xiaohong R, Bolla Manjeet K, Dennis Joe, Dunning Alison M, Easton Douglas F, Lush Michael, Michailidou Kyriaki, Pharoah Paul D P, Wang Qin, Adank Muriel A, Schmidt Marjanka K, Andrulis Irene L, Chang-Claude Jenny, Nevanlinna Heli, Chenevix-Trench Georgia, Evans D Gareth, Milne Roger L, Radice Paolo, Peterlongo Pao |
Genome-wide association study of executive function in a multi-ethnic cohort implicates LINC01362: Results from the northern Manhattan study.
Neurobiology of aging 2023 1 123 216-221. Dueker Nicole, Wang Liyong, Gardener Hannah, Gomez Lissette, Kaur Sonya, Beecham Ashley, Blanton Susan H, Dong Chuanhui, Gutierrez Jose, Cheung Ying Kuen, Moon Yeseon P, Levin Bonnie, Wright Clinton B, Elkind Mitchell S V, Sacco Ralph L, Rundek Tatja |
KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation. International journal of molecular sciences 2024 1 25 (2): . Antonia González-Garrido, Omar López-Ramírez, Abel Cerda-Mireles, Thania Navarrete-Miranda, Aranza Iztanami Flores-Arenas, Arturo Rojo-Domínguez, Leticia Arregui, Pedro Iturralde, Erika Antúnez-Argüelles, Mayra Domínguez-Pérez, Leonor Jacobo-Albavera, Alessandra Carnevale, Teresa Villarreal-Moli |
National Prevalence of Caprine Prion Protein Genetic Variability at Codons 146, 211, and 222 in Goat Herds in the United States. Veterinary sciences 2024 1 11 (1): . Mohamed Zeineldin, Heather Cox-Struble, Patrick Camp, David Farrell, Randy Pritchard, Tyler C Thacker, Kimberly Lehm |
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