Publications by authors named "Jordan Mike"

Article Synopsis
  • The article "Defining racial allies" by Hinger et al. investigates White allyship from the perspectives of Black, Indigenous, and people of color (BIPOC), aiming to create a framework that captures their views on racial allyship.
  • Utilizing constructivist grounded theory, the authors conducted focus groups to identify the key components of effective allyship, emphasizing the need for trust, antiracist action, and sociopolitical knowledge.
  • The findings encourage White counseling psychologists to integrate these concepts of racial allyship into their work, supporting a commitment to social justice and multiculturalism in the field.
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While interdisciplinary scholars and activists urge White allies to engage in racial justice work led by the voices of Black, Indigenous, and people of color (BIPOC), to date, most research on racial allyship has centered exclusively on the perspective of White allies themselves. Thus, the purpose of this study was to create a framework of racial allyship from the perspective of BIPOC. Utilizing constructivist grounded theory (Charmaz, 2014), focus groups were conducted to understand how BIPOC describe the knowledge, skills, and actions of White allies.

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Black transmasculine people are disproportionately affected by a myriad of intersecting stressors including racism (specifically anti-Black racism), sexism, and cissexism. Black transmasculine people are exposed daily to systemic oppression such as transphobia, dehumanization, and violence, making this community more vulnerable to mental health and physical health concerns. These experiences are further compounded by the lack of relevant research about the unique experiences of Black transmasculine people during the COVID-19 pandemic.

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Genetic testing has increased the number of variants identified in disease genes, but the diagnostic utility is limited by lack of understanding variant function. CARD11 encodes an adaptor protein that expresses dominant-negative and gain-of-function variants associated with distinct immunodeficiencies. Here, we used a "cloning-free" saturation genome editing approach in a diploid cell line to simultaneously score 2,542 variants for decreased or increased function in the region of CARD11 associated with immunodeficiency.

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