Translating Nature: The Discourse of Natural History in The Journals of the Lewis and Clark Expedition

Authors: Buckley, Michael G.

Source: Western American Literature. 43(1):25-40

Availability: https://muse.jhu.edu/article/535248

Philosophic Method in Cicero

Authors: Buckley, Michael J

Source: Journal of the History of Philosophy. 8(2):143-154

Availability: https://muse.jhu.edu/article/229370

The Idea of Justice (review)

Authors: Buckley, Michael

Source: The Journal of Speculative Philosophy. 26(1):73-75

Availability: https://muse.jhu.edu/article/479920

Integrated higher order Floquet mode meander line polarizer radome

Biallelic SLC13A1 loss-of-function variants result in impaired sulfate transport and skeletal phenotypes, including short stature, scoliosis, and skeletal dysplasia

Authors: Tise, Christina G. ^{1, ∗∗}, Ashton, Katie ², de Hayr, Lachlan ^{3, 4}, Lee, Kun-Di ⁵, Patkar, Omkar L. ⁵, Krzesinski, Emma ^{6, 7}, Bassetti, Jennifer A. ⁸, Carter, Erin M. ⁹, Raggio, Cathleen ⁹, Zankl, Andreas ^{10, 11, 12}, Khanshour, Anas M. ^{13, 14}, Atala, Kristhen N. ¹³, Rios, Jonathan J. ^{13, 15}, Wise, Carol A. ^{13, 15}, Zhu, Ying ², Zhang, Futao ², Roscioli, Tony ^{2, 16}, Buckley, Michael ², Harvey, Robert J. ^{3, 4, ∗}, Dawson, Paul A. ⁵

Source: In Genetics in Medicine Open 2025 3

Biallelic variants in GTF3C3 result in an autosomal recessive disorder with intellectual disability

Authors: De Hayr, Lachlan ^{1, 2}, Blok, Laura E.R. ³, Dias, Kerith-Rae ^{4, 5}, Long, Jingyi ³, Begemann, Anaïs ⁶, Moir, Robyn D. ⁷, Willis, Ian M. ⁷, Mocera, Martina ⁶, Siegel, Gabriele ⁶, Steindl, Katharina ⁶, Evans, Carey-Anne ^{4, 8}, Zhu, Ying ⁸, Zhang, Futao ⁸, Field, Michael ⁹, Ma, Alan ^{10, 11}, Adès, Lesley ^{10, 11}, Josephi-Taylor, Sarah ^{10, 11}, Pfundt, Rolph ³, Zaki, Maha S. ¹², Tomoum, Hoda ¹³, Gregor, Anne ^{14, 15}, Laube, Julia ⁶, Reis, André ¹⁵, Maddirevula, Sateesh ¹⁶, Hashem, Mais O. ¹⁶, Zweier, Markus ⁶, Alkuraya, Fowzan S. ^{16, 17}, Maroofian, Reza ¹⁸, Buckley, Michael F. ⁸, Gleeson, Joseph G. ^{19, 20}, Zweier, Christiane ^{14, 15}, Coll-Tané, Mireia ³, Koolen, David A. ³, Rauch, Anita ^{6, 21, 22}, Roscioli, Tony ^{4, 5, 8}, Schenck, Annette ³, Harvey, Robert J. ^{1, 2, ∗}

Source: In Genetics in Medicine January 2025 27(1)

Defining methods to improve eSource site start-up practices

Authors: Cramer, Amy E. ^a, King, Linda S. ^b, Buckley, Michael T. ^c, Casteleyn, Peter ^d, Ennis, Cory ^e, Hamidi, Muayad ^f, Rodrigues, Gonçalo M.C. ^g, Snyder, Denise C. ^h, Vattikola, Aruna ⁱ, Eisenstein, Eric L. ^{j, k, ⁎}

Source: In Contemporary Clinical Trials Communications December 2024 42

Long genetic and social isolation in Neanderthals before their extinction

Authors: Slimak, Ludovic ^{1, 22, ∗}, Vimala, Tharsika ^{2, 22}, Seguin-Orlando, Andaine ^{1, 2, 22, 23}, Metz, Laure ^{3, 4}, Zanolli, Clément ⁵, Joannes-Boyau, Renaud ⁶, Frouin, Marine ^{7, 8}, Arnold, Lee J. ⁹, Demuro, Martina ⁹, Devièse, Thibaut ¹⁰, Comeskey, Daniel ¹¹, Buckley, Michael ¹², Camus, Hubert ¹³, Muth, Xavier ¹⁴, Lewis, Jason E. ^{8, 15}, Bocherens, Hervé ¹⁶, Yvorra, Pascale ³, Tenailleau, Christophe ¹⁷, Duployer, Benjamin ¹⁷, Coqueugniot, Hélène ^{18, 21}, Dutour, Olivier ^{18, 21}, Higham, Thomas ^{19, 20}, Sikora, Martin ^{2, 24, ∗∗}

Source: In Cell Genomics 11 September 2024 4(9)

Assessing the influence of rural residence and economic distress on lower extremity risk stratification among diabetic foot ulcer patients utilizing the Wound, Ischemia, and Foot Infection (WIfI) classification system

Authors: Tasman, Jordan, Clegg, Devin J., Carver, Colten, Adabala, Saahit, Buckley, Michael R., Goldman, Mitchell H., Roberson, Patricia N.E.

Source: In Journal of Diabetes and Its Complications August 2024 38(8)

Narrowing the diagnostic gap: Genomes, episignatures, long-read sequencing, and health economic analyses in an exome-negative intellectual disability cohort

Authors: Dias, Kerith-Rae, Shrestha, Rupendra, Schofield, Deborah, Evans, Carey-Anne, O’Heir, Emily, Zhu, Ying, Zhang, Futao, Standen, Krystle, Weisburd, Ben, Stenton, Sarah L., Sanchis-Juan, Alba, Brand, Harrison, Talkowski, Michael E., Ma, Alan, Ghedia, Sondy, Wilson, Meredith, Sandaradura, Sarah A., Smith, Janine, Kamien, Benjamin, Turner, Anne, Bakshi, Madhura, Adès, Lesley C., Mowat, David, Regan, Matthew, McGillivray, George, Savarirayan, Ravi, White, Susan M., Tan, Tiong Yang, Stark, Zornitza, Brown, Natasha J., Pérez-Jurado, Luis A., Krzesinski, Emma, Hunter, Matthew F., Akesson, Lauren, Fennell, Andrew Paul, Yeung, Alison, Boughtwood, Tiffany, Ewans, Lisa J., Kerkhof, Jennifer, Lucas, Christopher, Carey, Louise, French, Hugh, Rapadas, Melissa, Stevanovski, Igor, Deveson, Ira W., Cliffe, Corrina, Elakis, George, Kirk, Edwin P., Dudding-Byth, Tracy, Fletcher, Janice, Walsh, Rebecca, Corbett, Mark A., Kroes, Thessa, Gecz, Jozef, Meldrum, Cliff, Cliffe, Simon, Wall, Meg, Lunke, Sebastian, North, Kathryn, Amor, David J., Field, Michael, Sadikovic, Bekim, Buckley, Michael F., O’Donnell-Luria, Anne, Roscioli, Tony

Source: In Genetics in Medicine May 2024 26(5)

A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

Authors: Strong, Alanna, Rao, Soumya, Hardenberg, Sandra, Li, Dong, Cox, Liza L., Lee, Paul C., Zhang, Li Q., Awotoye, Waheed, Diamond, Tamir, Gold, Jessica, Gooch, Catherine, Gowans, Lord Jephthah Joojo, Hakonarson, Hakon, Hing, Anne, Loomes, Kathleen, Martin, Nicole, Selvanayagam, Thanuja, Marazita, Mary L., Mononen, Tarja, Piccoli, David, Pfundt, Rolph, Raskin, Salmo, Scherer, Stephen W., Sobriera, Nara, Vaccaro, Courtney, Wang, Xiang, Watson, Deborah, Weksberg, Rosanna, Bhoj, Elizabeth, Murray, Jeffrey C., Lidral, Andrew C., Butali, Azeez, Buckley, Michael F., Roscioli, Tony, Koolen, David A., Seaver, Laurie H., Prows, Cynthia A., Stottmann, Rolf W., Cox, Timothy C.

Source: American journal of medical genetics.Part A. 191(5):1227-1239

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100194505123.0x000001&indx=1&recIds=ETOCvdc_100194505123.0x000001

Biallelic variants in TUBGCP6 result in microcephaly and chorioretinopathy 1: Report of four cases and a literature review

Authors: Thomas‐Wilson, Amanda, Schacht, John P., Chitayat, David, Blaser, Susan, Santos, Francis Jeshira Reynoso, Glaser, Kimberly, Caffo, Alesky, Wentzensen, Ingrid M., Henderson, Lindsay B., Zhang, Futao, Zhu, Ying, Di Corleto, Ellen, da Silva Costa, Fabricio, Vink, Rebecca, Alkhunaizi, Ebba, Russell, Laura, Buckley, Michael F., Roscioli, Tony, Pereira, Elaine Maria, Ganapathi, Mythily

Source: American journal of medical genetics.Part A. 191(7):1935-1941

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100194279766.0x000001&indx=1&recIds=ETOCvdc_100194279766.0x000001

Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer‐specific survival

Authors: Morra, Anna, Schreurs, Maartje A. C., Andrulis, Irene L., Anton‐Culver, Hoda, Augustinsson, Annelie, Beckmann, Matthias W., Behrens, Sabine, Bojesen, Stig E., Bolla, Manjeet K., Brauch, Hiltrud, Broeks, Annegien, Buys, Saundra S., Camp, Nicola J., Castelao, Jose E., Cessna, Melissa H., Chang‐Claude, Jenny, Chung, Wendy K., Sahlberg, Kristine K., Børresen‐Dale, Anne‐Lise, Gram, Inger Torhild, Olsen, Karina Standahl, Engebråten, Olav, Naume, Bjørn, Geisler, Jürgen, Grenaker Alnæs, Grethe I., Colonna, Sarah V., Couch, Fergus J., Cox, Angela, Cross, Simon S., Czene, Kamila, Daly, Mary B., Dennis, Joe, Devilee, Peter, Dörk, Thilo, Dunning, Alison M., Dwek, Miriam, Easton, Douglas F., Eccles, Diana M., Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A., Fehm, Tanja N., Figueroa, Jonine D., Flyger, Henrik, Gabrielson, Marike, Gago‐Dominguez, Manuela, García‐Closas, Montserrat, García‐Sáenz, José A., Genkinger, Jeanine, Grassmann, Felix, Gündert, Melanie, Hahnen, Eric, Haiman, Christopher A., Hamann, Ute, Harrington, Patricia A., Hartikainen, Jaana M., Hoppe, Reiner, Hopper, John L., Houlston, Richard S., Howell, Anthony, Clarke, Christine, Marsh, Deborah, Scott, Rodney, Baxter, Robert, Yip, Desmond, Carpenter, Jane, Davis, Alison, Pathmanathan, Nirmala, Simpson, Peter, Graham, J. Dinny, Sachchithananthan, Mythily, Amor, David, Andrews, Lesley, Antill, Yoland, Balleine, Rosemary, Beesley, Jonathan, Bennett, Ian, Bogwitz, Michael, Botes, Leon, Brennan, Meagan, Brown, Melissa, Buckley, Michael, Burke, Jo, Butow, Phyllis, Caldon, Liz, Campbell, Ian, Cao, Michelle, Chakrabarti, Anannya, Chauhan, Deepa, Chauhan, Manisha, Chenevix‐Trench, Georgia, Christian, Alice, Cohen, Paul, Colley, Alison, Crook, Ashley, Cui, James, Courtney, Eliza, Cummings, Margaret, Dawson, Sarah‐Jane, DeFazio, Anna, Delatycki, Martin, Dickson, Rebecca, Dixon, Joanne, Edkins, Ted, Edwards, Stacey, Farshid, Gelareh, Fellows, Andrew, Fenton, Georgina, Field, Michael, Flanagan, James, Fong, Peter, Forrest, Laura, Fox, Stephen, French, Juliet, Friedlander, Michael, Gaff, Clara, Gattas, Mike, George, Peter, Greening, Sian, Harris, Marion, Hart, Stewart, Hayward, Nick, Hopper, John, Hoskins, Cass, Hunt, Clare, James, Paul, Jenkins, Mark, Kidd, Alexa, Kirk, Judy, Koehler, Jessica, Kollias, James, Lakhani, Sunil, Lawrence, Mitchell, Lee, Jason, Li, Shuai, Lindeman, Geoff, Lipton, Lara, Lobb, Liz, Loi, Sherene, Mann, Graham, McLachlan, Sue Anne, Meiser, Bettina, Milne, Roger, Nightingale, Sophie, O'Connell, Shona, O'Sullivan, Sarah, Ortega, David Gallego, Pachter, Nick, Pang, Jia‐Min, Pathak, Gargi, Patterson, Briony, Pearn, Amy, Phillips, Kelly, Pieper, Ellen, Ramus, Susan, Rickard, Edwina, Robinson, Bridget, Saleh, Mona, Skandarajah, Anita, Salisbury, Elizabeth, Saunders, Christobel, Saunus, Jodi, Scott, Clare, Sexton, Adrienne, Shelling, Andrew, Southey, Melissa, Spurdle, Amanda, Taylor, Jessica, Taylor, Renea, Thorne, Heather, Trainer, Alison, Tucker, Kathy, Visvader, Jane, Walker, Logan, Williams, Rachael, Winship, Ingrid, Young, Mary Ann, Zaheed, Milita, Jakubowska, Anna, Janni, Wolfgang, Jernström, Helena, John, Esther M., Johnson, Nichola, Jones, Michael E., Kristensen, Vessela N., Kurian, Allison W., Lambrechts, Diether, Le Marchand, Loic, Lindblom, Annika, Lubiński, Jan, Lux, Michael P., Mannermaa, Arto, Mavroudis, Dimitrios, Mulligan, Anna Marie, Muranen, Taru A., Nevanlinna, Heli, Nevelsteen, Ines, Neven, Patrick, Newman, William G., Obi, Nadia, Offit, Kenneth, Olshan, Andrew F., Park‐Simon, Tjoung‐Won, Patel, Alpa V., Peterlongo, Paolo, Phillips, Kelly‐Anne, Plaseska‐Karanfilska, Dijana, Polley, Eric C., Presneau, Nadege, Pylkäs, Katri, Rack, Brigitte, Radice, Paolo, Rashid, Muhammad U., Rhenius, Valerie, Robson, Mark, Romero, Atocha, Saloustros, Emmanouil, Sawyer, Elinor J., Schmutzler, Rita K., Schuetze, Sabine, Scott, Christopher, Shah, Mitul, Smichkoska, Snezhana, Southey, Melissa C., Tapper, William J., Teras, Lauren R., Tollenaar, Rob A. E. M., Tomczyk, Katarzyna, Tomlinson, Ian, Troester, Melissa A., Vachon, Celine M., Veen, Elke M., Wang, Qin, Wendt, Camilla, Wildiers, Hans, Winqvist, Robert, Ziogas, Argyrios, Hall, Per, Pharoah, Paul D. P., Adank, Muriel A., Hollestelle, Antoinette, Schmidt, Marjanka K., Hooning, Maartje J.

Source: Cancer medicine. 12(15):16142-16162

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100191750966.0x000001&indx=1&recIds=ETOCvdc_100191750966.0x000001

The clinical and molecular spectrum of the KDM6B-related neurodevelopmental disorder

Authors: Rots, Dmitrijs, Jakub, Taryn E., Keung, Crystal, Jackson, Adam, Banka, Siddharth, Pfundt, Rolph, de Vries, Bert B.A., van Jaarsveld, Richard H., Hopman, Saskia M.J., van Binsbergen, Ellen, Valenzuela, Irene, Hempel, Maja, Bierhals, Tatjana, Kortüm, Fanny, Lecoquierre, Francois, Goldenberg, Alice, Hertz, Jens Michael, Andersen, Charlotte Brasch, Kibæk, Maria, Prijoles, Eloise J., Stevenson, Roger E., Everman, David B., Patterson, Wesley G., Meng, Linyan, Gijavanekar, Charul, De Dios, Karl, Lakhani, Shenela, Levy, Tess, Wagner, Matias, Wieczorek, Dagmar, Benke, Paul J., Lopez Garcia, María Soledad, Perrier, Renee, Sousa, Sergio B., Almeida, Pedro M., Simões, Maria José, Isidor, Bertrand, Deb, Wallid, Schmanski, Andrew A., Abdul-Rahman, Omar, Philippe, Christophe, Bruel, Ange-Line, Faivre, Laurence, Vitobello, Antonio, Thauvin, Christel, Smits, Jeroen J., Garavelli, Livia, Caraffi, Stefano G., Peluso, Francesca, Davis-Keppen, Laura, Platt, Dylan, Royer, Erin, Leeuwen, Lisette, Sinnema, Margje, Stegmann, Alexander P.A., Stumpel, Constance T.R.M., Tiller, George E., Bosch, Daniëlle G.M., Potgieter, Stephanus T., Joss, Shelagh, Splitt, Miranda, Holden, Simon, Prapa, Matina, Foulds, Nicola, Douzgou, Sofia, Puura, Kaija, Waltes, Regina, Chiocchetti, Andreas G., Freitag, Christine M., Satterstrom, F. Kyle, De Rubeis, Silvia, Buxbaum, Joseph, Gelb, Bruce D., Branko, Aleksic, Kushima, Itaru, Howe, Jennifer, Scherer, Stephen W., Arado, Alessia, Baldo, Chiara, Patat, Olivier, Bénédicte, Demeer, Lopergolo, Diego, Santorelli, Filippo M., Haack, Tobias B., Dufke, Andreas, Bertrand, Miriam, Falb, Ruth J., Rieß, Angelika, Krieg, Peter, Spranger, Stephanie, Bedeschi, Maria Francesca, Iascone, Maria, Josephi-Taylor, Sarah, Roscioli, Tony, Buckley, Michael F., Liebelt, Jan, Dagli, Aditi I., Aten, Emmelien, Hurst, Anna C.E., Hicks, Alesha, Suri, Mohnish, Aliu, Ermal, Naik, Sunil, Sidlow, Richard, Coursimault, Juliette, Nicolas, Gaël, Küpper, Hanna, Petit, Florence, Ibrahim, Veyan, Top, Deniz, Di Cara, Francesca, Louie, Raymond J., Stolerman, Elliot, Brunner, Han G., Vissers, Lisenka E.L.M., Kramer, Jamie M., Kleefstra, Tjitske

Source: American journal of human genetics. 110(6):963-978

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100191548842.0x000001&indx=1&recIds=ETOCvdc_100191548842.0x000001

Bi-allelic TTI1 variants cause an autosomal-recessive neurodevelopmental disorder with microcephaly

Authors: Serey-Gaut, Margaux, Cortes, Marisol, Makrythanasis, Periklis, Suri, Mohnish, Taylor, Alexander M.R., Sullivan, Jennifer A., Asleh, Ayat N., Mitra, Jaba, Dar, Mohamad A., McNamara, Amy, Shashi, Vandana, Dugan, Sarah, Song, Xiaofei, Rosenfeld, Jill A., Cabrol, Christelle, Iwaszkiewicz, Justyna, Zoete, Vincent, Pehlivan, Davut, Akdemir, Zeynep Coban, Roeder, Elizabeth R., Littlejohn, Rebecca Okashah, Dibra, Harpreet K., Byrd, Philip J., Stewart, Grant S., Geckinli, Bilgen B., Posey, Jennifer, Westman, Rachel, Jungbluth, Chelsy, Eason, Jacqueline, Sachdev, Rani, Evans, Carey-Anne, Lemire, Gabrielle, VanNoy, Grace E., O'Donnell-Luria, Anne, Mau-Them, Frédéric Tran, Juven, Aurélien, Piard, Juliette, Nixon, Cheng Yee, Zhu, Ying, Ha, Taekjip, Buckley, Michael F., Thauvin, Christel, Essien Umanah, George K., Van Maldergem, Lionel, Lupski, James R., Roscioli, Tony, Dawson, Valina L., Dawson, Ted M., Antonarakis, Stylianos E.

Source: American journal of human genetics. 110(3):499-515

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100184726580.0x000001&indx=1&recIds=ETOCvdc_100184726580.0x000001

Exploring Diversity in Neolithic Agropastoral Management in Mainland Greece Using Stable Isotope Analysis

Authors: Vaiglova, Petra, Coleman, John, Diffey, Charlotte, Tzevelekidi, Vasiliki, Fillios, Melanie, Pappa, Maria, Halstead, Paul, Valamoti, Soultana Maria, Cavanagh, William, Renard, Josette, Buckley, Michael, Bogaard, Amy

Source: Environmental archaeology. 28(2):62-85

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100176803857.0x000001&indx=1&recIds=ETOCvdc_100176803857.0x000001

Irony and the “We” in Hegel's Phenomenology of Spirit.

Authors: Buckley, Michael

Source: Clio; Spring2002, Vol. 31 Issue 3, p279-300, 22p

Efficient GPU Computing Framework of Cloud Filtering in Remotely Sensed Image Processing

Authors: Ke, Jing, Sowmya, Arcot, Guo, Yi, Bednarz, Tomasz, Buckley, Michael

Source: 2016 International Conference on Digital Image Computing: Techniques and Applications (DICTA) Digital Image Computing: Techniques and Applications (DICTA), 2016 International Conference on. :1-8 Nov, 2016

Relation: 2016 International Conference on Digital Image Computing: Techniques and Applications (DICTA)

Dominant-negative variants in CBX1 cause a neurodevelopmental disorder

Authors: Kuroda, Yukiko, Iwata-Otsubo, Aiko, Dias, Kerith-Rae, Temple, Suzanna E.L., Nagao, Koji, De Hayr, Lachlan, Zhu, Ying, Isobe, Shin-Ya, Nishibuchi, Gohei, Fiordaliso, Sarah K., Fujita, Yuki, Rippert, Alyssa L., Baker, Samuel W., Leung, Marco L., Koboldt, Daniel C., Harman, Adele, Keena, Beth A., Kazama, Izumi, Subramanian, Gopinath Musuwadi, Manickam, Kandamurugu, Schmalz, Betsy, Latsko, Maeson, Zackai, Elaine H., Edwards, Matt, Evans, Carey-Anne, Dulik, Matthew C., Buckley, Michael F., Yamashita, Toshihide, O'Brien, W. Timothy, Harvey, Robert J., Obuse, Chikashi, Roscioli, Tony, Izumi, Kosuke

Source: In Genetics in Medicine July 2023 25(7)

Machine Learning for collagen peptide biomarker determination in the taxonomic identification of archaeological fish remains

Authors: Baker, Andrew, Harvey, Virginia L., Buckley, Michael

Source: In Journal of Archaeological Science: Reports June 2023 49