fhdfgh - Earth Sciences bibliographies - in Harvard style

In-text: (Dungu et al., 2021)

Your Bibliography: Dungu, J., Langley, S., Hardy-Wallace, A., Li, B., Barbagallo, R., Field, D., Homfray, T. and Savage, H., 2021. Dilated cardiomyopathy: the role of genetics, highlighted in a family with Filamin C (FLNC) variant. Heart, [online] 108(9), pp.676-682. Available at: <https://www.proquest.com/docview/2648624509?accountid=13380&pq-origsite=primo> [Accessed 24 September 2022].

In-text: (Ebili et al., 2017)

Your Bibliography: Ebili, H., Hassall, J., Fadhil, W., Ham-Karim, H., Asiri, A., Raposo, T., Agboola, A. and Ilyas, M., 2017. “Squirrel” Primer-Based PCR Assay for Direct and Targeted Sanger Sequencing of Short Genomic Segments. Journal of Biomolecular Techniques : JBT, [online] 28(3), pp.97-110. Available at: <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460669/> [Accessed 24 September 2022].

In-text: (Firth et al., 2009)

Your Bibliography: Firth, H., Richards, S., Bevan, A., Clayton, S., Corpas, M., Rajan, D., Vooren, S., Moreau, Y., Pettett, R. and Carter, N., 2009. DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. The American Journal of Human Genetics, [online] 84(4), pp.524-533. Available at: <https://www.cell.com/ajhg/fulltext/S0002-9297(09)00107-4> [Accessed 24 September 2022].

In-text: (Karczewski et al., 2020)

Your Bibliography: Karczewski, K., Francioli, L., Tiao, G., Cummings, B., Alföldi, J., Wang, Q., Collins, R., Laricchia, K., Ganna, A., Birnbaum, D., Gauthier, L., Brand, H., Solomonson, M., Watts, N., Rhodes, D., Singer-Berk, M., England, E., Seaby, E., Kosmicki, J., Walters, R., Tashman, K., Farjoun, Y., Banks, E., Poterba, T., Wang, A., Seed, C., Whiffin, N., Chong, J., Samocha, K., Pierce-Hoffman, E., Zappala, Z., O’Donnell-Luria, A., Minikel, E., Weisburd, B., Lek, M., Ware, J., Vittal, C., Armean, I., Bergelson, L., Cibulskis, K., Connolly, K., Covarrubias, M., Donnelly, S., Ferriera, S., Gabriel, S., Gentry, J., Gupta, N., Jeandet, T., Kaplan, D., Llanwarne, C., Munshi, R., Novod, S., Petrillo, N., Roazen, D., Ruano-Rubio, V., Saltzman, A., Schleicher, M., Soto, J., Tibbetts, K., Tolonen, C., Wade, G., Talkowski, M., Aguilar Salinas, C., Ahmad, T., Albert, C., Ardissino, D., Atzmon, G., Barnard, J., Beaugerie, L., Benjamin, E., Boehnke, M., Bonnycastle, L., Bottinger, E., Bowden, D., Bown, M., Chambers, J., Chan, J., Chasman, D., Cho, J., Chung, M., Cohen, B., Correa, A., Dabelea, D., Daly, M., Darbar, D., Duggirala, R., Dupuis, J., Ellinor, P., Elosua, R., Erdmann, J., Esko, T., Färkkilä, M., Florez, J., Franke, A., Getz, G., Glaser, B., Glatt, S., Goldstein, D., Gonzalez, C., Groop, L., Haiman, C., Hanis, C., Harms, M., Hiltunen, M., Holi, M., Hultman, C., Kallela, M., Kaprio, J., Kathiresan, S., Kim, B., Kim, Y., Kirov, G., Kooner, J., Koskinen, S., Krumholz, H., Kugathasan, S., Kwak, S., Laakso, M., Lehtimäki, T., Loos, R., Lubitz, S., Ma, R., MacArthur, D., Marrugat, J., Mattila, K., McCarroll, S., McCarthy, M., McGovern, D., McPherson, R., Meigs, J., Melander, O., Metspalu, A., Neale, B., Nilsson, P., O’Donovan, M., Ongur, D., Orozco, L., Owen, M., Palmer, C., Palotie, A., Park, K., Pato, C., Pulver, A., Rahman, N., Remes, A., Rioux, J., Ripatti, S., Roden, D., Saleheen, D., Salomaa, V., Samani, N., Scharf, J., Schunkert, H., Shoemaker, M., Sklar, P., Soininen, H., Sokol, H., Spector, T., Sullivan, P., Suvisaari, J., Tai, E., Teo, Y., Tiinamaija, T., Tsuang, M., Turner, D., Tusie-Luna, T., Vartiainen, E., Vawter, M., Ware, J., Watkins, H., Weersma, R., Wessman, M., Wilson, J., Xavier, R., Neale, B., Daly, M. and MacArthur, D., 2020. The mutational constraint spectrum quantified from variation in 141,456 humans. Nature, [online] 581(7809), pp.434-443. Available at: <https://www.nature.com/articles/s41586-020-2308-7#citeas> [Accessed 24 September 2022].

In-text: (Landrum et al., 2017)

Your Bibliography: Landrum, M., Lee, J., Benson, M., Brown, G., Chao, C., Chitipiralla, S., Gu, B., Hart, J., Hoffman, D., Jang, W., Karapetyan, K., Katz, K., Liu, C., Maddipatla, Z., Malheiro, A., McDaniel, K., Ovetsky, M., Riley, G., Zhou, G., Holmes, J., Kattman, B. and Maglott, D., 2017. ClinVar: improving access to variant interpretations and supporting evidence. Nucleic Acids Research, [online] 46(D1), pp.D1062-D1067. Available at: <https://pubmed.ncbi.nlm.nih.gov/29165669/> [Accessed 24 September 2022].

In-text: (Marian and Braunwald, 2017)

Your Bibliography: Marian, A. and Braunwald, E., 2017. Hypertrophic Cardiomyopathy. Circulation Research, [online] 121(7), pp.749-770. Available at: <https://www.ahajournals.org/doi/pdf/10.1161/CIRCRESAHA.117.311059> [Accessed 24 September 2022].

In-text: (Muchtar, Blauwet and Gertz, 2017)

Your Bibliography: Muchtar, E., Blauwet, L. and Gertz, M., 2017. Restrictive Cardiomyopathy. Circulation Research, [online] 121(7), pp.819-837. Available at: <https://www.ahajournals.org/doi/pdf/10.1161/CIRCRESAHA.117.310982> [Accessed 24 September 2022].

In-text: (Nozari et al., 2018)

Your Bibliography: Nozari, A., Aghaei-Moghadam, E., Zeinaloo, A., Mollazadeh, R., Majnoon, M., Alavi, A., Ghasemi Firouzabadi, S., Mohammadzadeh, A., Banihashemi, S., Nikzaban, M., Najmabadi, H. and Behjati, F., 2018. A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family. Gene, [online] 659, pp.160-167. Available at: <https://www.sciencedirect.com/science/article/pii/S0378111918302828> [Accessed 24 September 2022].

In-text: (O'Leary et al., 2015)

Your Bibliography: O'Leary, N., Wright, M., Brister, J., Ciufo, S., Haddad, D., McVeigh, R., Rajput, B., Robbertse, B., Smith-White, B., Ako-Adjei, D., Astashyn, A., Badretdin, A., Bao, Y., Blinkova, O., Brover, V., Chetvernin, V., Choi, J., Cox, E., Ermolaeva, O., Farrell, C., Goldfarb, T., Gupta, T., Haft, D., Hatcher, E., Hlavina, W., Joardar, V., Kodali, V., Li, W., Maglott, D., Masterson, P., McGarvey, K., Murphy, M., O'Neill, K., Pujar, S., Rangwala, S., Rausch, D., Riddick, L., Schoch, C., Shkeda, A., Storz, S., Sun, H., Thibaud-Nissen, F., Tolstoy, I., Tully, R., Vatsan, A., Wallin, C., Webb, D., Wu, W., Landrum, M., Kimchi, A., Tatusova, T., DiCuccio, M., Kitts, P., Murphy, T. and Pruitt, K., 2015. Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation. Nucleic Acids Research, [online] 44(D1), pp.D733-D745. Available at: <https://pubmed.ncbi.nlm.nih.gov/26553804/> [Accessed 24 September 2022].

In-text: (Ortiz-Genga et al., 2016)

Your Bibliography: Ortiz-Genga, M., Cuenca, S., Dal Ferro, M., Zorio, E., Salgado-Aranda, R., Climent, V., Padrón-Barthe, L., Duro-Aguado, I., Jiménez-Jáimez, J., Hidalgo-Olivares, V., García-Campo, E., Lanzillo, C., Suárez-Mier, M., Yonath, H., Marcos-Alonso, S., Ochoa, J., Santomé, J., García-Giustiniani, D., Rodríguez-Garrido, J., Domínguez, F., Merlo, M., Palomino, J., Peña, M., Trujillo, J., Martín-Vila, A., Stolfo, D., Molina, P., Lara-Pezzi, E., Calvo-Iglesias, F., Nof, E., Calò, L., Barriales-Villa, R., Gimeno-Blanes, J., Arad, M., García-Pavía, P. and Monserrat, L., 2016. Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic Cardiomyopathies. Journal of the American College of Cardiology, [online] 68(22), pp.2440-2451. Available at: <https://www.sciencedirect.com/science/article/pii/S0735109716364166?via%3Dihub> [Accessed 24 September 2022].

In-text: (Schultheiss et al., 2019)

Your Bibliography: Schultheiss, H., Fairweather, D., Caforio, A., Escher, F., Hershberger, R., Lipshultz, S., Liu, P., Matsumori, A., Mazzanti, A., McMurray, J. and Priori, S., 2019. Dilated cardiomyopathy. Nature Reviews Disease Primers, [online] 5(1). Available at: <https://www.nature.com/articles/s41572-019-0084-1#citeas> [Accessed 24 September 2022].

In-text: (Schwarz, Cooper, Schuelke and Seelow, 2014)

Your Bibliography: Schwarz, J., Cooper, D., Schuelke, M. and Seelow, D., 2014. MutationTaster2: mutation prediction for the deep-sequencing age. Nature Methods, [online] 11(4), pp.361-362. Available at: <https://www.nature.com/articles/nmeth.2890#citeas> [Accessed 24 September 2022].

In-text: (Sveinbjornsson et al., 2018)

Your Bibliography: Sveinbjornsson, G., Olafsdottir, E., Thorolfsdottir, R., Davidsson, O., Helgadottir, A., Jonasdottir, A., Jonasdottir, A., Bjornsson, E., Jensson, B., Arnadottir, G., Kristinsdottir, H., Stephensen, S., Oskarsson, G., Gudbjartsson, T., Sigurdsson, E., Andersen, K., Danielsen, R., Arnar, D., Jonsdottir, I., Thorsteinsdottir, U., Sulem, P., Thorgeirsson, G., Gudbjartsson, D., Holm, H. and Stefansson, K., 2018. Variants inNKX2-5andFLNCCause Dilated Cardiomyopathy and Sudden Cardiac Death. Circulation: Genomic and Precision Medicine, [online] 11(8). Available at: <https://www.ahajournals.org/doi/pdf/10.1161/CIRCGEN.117.002151> [Accessed 24 September 2022].

In-text: (Verdonschot et al., 2020)

Your Bibliography: Verdonschot, J., Vanhoutte, E., Claes, G., Helderman‐van den Enden, A., Hoeijmakers, J., Hellebrekers, D., Haan, A., Christiaans, I., Lekanne Deprez, R., Boen, H., Craenenbroeck, E., Loeys, B., Hoedemaekers, Y., Marcelis, C., Kempers, M., Brusse, E., Waning, J., Baas, A., Dooijes, D., Asselbergs, F., Barge‐Schaapveld, D., Koopman, P., Wijngaard, A., Heymans, S., Krapels, I. and Brunner, H., 2020. A mutation update for the FLNC gene in myopathies and cardiomyopathies. Human Mutation, [online] 41(6), pp.1091-1111. Available at: <https://onlinelibrary.wiley.com/doi/full/10.1002/humu.24004> [Accessed 24 September 2022].

In-text: (Ye et al., 2012)

Your Bibliography: Ye, J., Coulouris, G., Zaretskaya, I., Cutcutache, I., Rozen, S. and Madden, T., 2012. Primer-BLAST: A tool to design target-specific primers for polymerase chain reaction. BMC Bioinformatics, [online] 13(1). Available at: <https://pubmed.ncbi.nlm.nih.gov/22708584/> [Accessed 24 September 2022].