Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations von Giardine, Belinda M, Joly, Philippe, Pissard, Serge, Wajcman, Henri, K. Chui, David H, Hardison, Ross C, Patrinos, George P

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Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab‐Indian haplotype is not benign von Alsultan, Abdulrahman, Alabdulaali, Mohammed K., Griffin, Paula J., AlSuliman, Ahmed M., Ghabbour, Hazem A., Sebastiani, Paola, Albuali, Waleed H., Al‐Ali, Amein K., Chui, David H. K., Steinberg, Martin H.

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Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin von Ngo, Duyen A., Aygun, Banu, Akinsheye, Idowu, Hankins, Jane S., Bhan, Ishir, Luo, Hong Y., Steinberg, Martin H., Chui, David H. K.

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Fetal hemoglobin in sickle cell anemia von Akinsheye, Idowu, Alsultan, Abdulrahman, Solovieff, Nadia, Ngo, Duyen, Baldwin, Clinton T., Sebastiani, Paola, Chui, David H.K., Steinberg, Martin H.

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Notch and Aryl Hydrocarbon Receptor Signaling Impact Definitive Hematopoiesis from Human Pluripotent Stem Cells von Leung, Amy, Zulick, Elizabeth, Skvir, Nicholas, Vanuytsel, Kim, Morrison, Tasha A., Naing, Zaw Htut, Wang, Zhongyan, Dai, Yan, Chui, David H. K., Steinberg, Martin H., Sherr, David H., Murphy, George J.

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The aryl hydrocarbon receptor directs hematopoietic progenitor cell expansion and differentiation von Smith, Brenden W., Rozelle, Sarah S., Leung, Amy, Ubellacker, Jessalyn, Parks, Ashley, Nah, Shirley K., French, Deborah, Gadue, Paul, Monti, Stefano, Chui, David H.K., Steinberg, Martin H., Frelinger, Andrew L., Michelson, Alan D., Theberge, Roger, McComb, Mark E., Costello, Catherine E., Kotton, Darrell N., Mostoslavsky, Gustavo, Sherr, David H., Murphy, George J.

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MS Analysis of Single-Nucleotide Differences in Circulating Nucleic Acids: Application to Noninvasive Prenatal Diagnosis von Ding, Chunming, Rossa W. K. Chiu, Lau, Tze K., Leung, Tse N., Chan, Li C., Amy Y. Y. Chan, Charoenkwan, Pimlak, Ivy S. L. Ng, Law, Hai-yang, Edmond S. K. Ma, Xu, Xiangmin, Wanapirak, Chanane, Sanguansermsri, Torpong, Liao, Can, Mary Anne Tan Jin Ai, David H. K. Chui, Cantor, Charles R., Y. M. Dennis Lo

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Hemoglobin H disease: not necessarily a benign disorder von Chui, DavidH.K., Fucharoen, Suthat, Chan, Vivian

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The effects of hydroxycarbamide and magnesium on haemoglobin SC disease: results of the multi‐centre CHAMPS trial von Wang, Winfred, Brugnara, Carlo, Snyder, Cathie, Wynn, Lynn, Rogers, Zora, Kalinyak, Karen, Brown, Clark, Qureshi, Asif, Bigelow, Carolyn, Neumayr, Lynne, Smith‐Whitley, Kim, Chui, David H. K., Delahunty, Mardee, Woolson, Rob, Steinberg, Martin, Telen, Marilyn, Kesler, Karen

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A phase 2 study of HQK‐1001, an oral fetal haemoglobin inducer, in β‐thalassaemia intermedia von Inati, Adlette, Kahale, Mario, Perrine, Susan P., Chui, David H. K., Taher, Ali T., Koussa, Suzanne, Abi Nasr, Therese, Abbas, Hussein A., Ghalie, Richard G.

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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster von Solovieff, Nadia, Milton, Jacqueline N., Hartley, Stephen W., Sherva, Richard, Sebastiani, Paola, Dworkis, Daniel A., Klings, Elizabeth S., Farrer, Lindsay A., Garrett, Melanie E., Ashley-Koch, Allison, Telen, Marilyn J., Fucharoen, Supan, Ha, Shau Yin, Li, Chi-Kong, Chui, David H.K., Baldwin, Clinton T., Steinberg, Martin H.

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Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans von Alsultan, Abdulrahman, Solovieff, Nadia, Aleem, Aamer, AlGahtani, Farjah H., Al‐Shehri, Ali, Elfaki Osman, Mohamed, Kurban, Kadijah, Bahakim, Hasan, Kareem Al‐Momen, Abdul, Baldwin, Clinton T., Chui, David H.K., Steinberg, Martin H.

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A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression von Farrell, John J., Sherva, Richard M., Chen, Zhi-yi, Luo, Hong-yuan, Chu, Benjamin F., Ha, Shau Yin, Li, Chi Kong, Lee, Anselm C.W., Li, Rever C.H., Li, Chi Keung, Yuen, Hui Leung, So, Jason C.C., Ma, Edmond S.K., Chan, Li Chong, Chan, Vivian, Sebastiani, Paola, Farrer, Lindsay A., Baldwin, Clinton T., Steinberg, Martin H., Chui, David H.K.

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Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies von Patrinos, George P., Giardine, Belinda, Riemer, Cathy, Miller, Webb, Chui, David H. K., Anagnou, Nicholas P., Wajcman, Henri, Hardison, Ross C.

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Fetal hemoglobin in sickle cell anemia: a glass half full? von Steinberg, Martin H., Chui, David H.K., Dover, George J., Sebastiani, Paola, Alsultan, Abdulrahman

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Diverse hematological phenotypes of β-thalassemia carriers von Luo, Hong-Yuan, Chui, David H.K.

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A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F von Chen, Zhiyi, Luo, Hong-Yuan, Basran, Raveen K., Hsu, Tien-Huei, Mang, Daniel W. H., Nuntakarn, Lalana, Rosenfield, Cathy G., Patrinos, George P., Hardison, Ross C., Steinberg, Martin H., Chui, David H. K.

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HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update von Giardine, Belinda, van Baal, Sjozef, Kaimakis, Polynikis, Riemer, Cathy, Miller, Webb, Samara, Maria, Kollia, Panagoula, Anagnou, Nicholas P., Chui, David H.K., Wajcman, Henri, Hardison, Ross C., Patrinos, George P.

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MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies von Théberge, Roger, Dikler, Sergei, Heckendorf, Christian, Chui, David H. K., Costello, Catherine E., McComb, Mark E.

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Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: A systematic review von Verhovsek, Madeleine, Henderson, Matthew P.A., Cox, Gerard, Luo, Hong‐yuan, Steinberg, Martin H., Chui, David H.K.

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