Lainie Friedman Ross
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American physician and bioethicist
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Lainie Friedman Rossphilosophy Degrees
Philosophy
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Bioethics
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Philosophy
Lainie Friedman Ross's Degrees
- Doctorate Medicine University of Chicago
- PhD Bioethics University of Chicago
Why Is Lainie Friedman Ross Influential?
(Suggest an Edit or Addition)According to Wikipedia, Lainie Friedman Ross is an American physician and bioethicist who works at the University of Chicago. Early life Lainie Friedman Ross is a 1982 graduate of Princeton University where she majored in the Woodrow Wilson School of Public and International Affairs. She has a medical degree from the University of Pennsylvania, and she also obtained an M.Phil and a PhD in philosophy from Yale University.
Lainie Friedman Ross's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Recommendations for returning genomic incidental findings? We need to talk! (2013) (275)
- Ethics of a paired-kidney-exchange program. (1997) (192)
- Cochlear Implants in Adults and Children (1995) (173)
- The Challenges of Collaboration for Academic and Community Partners in a Research Partnership: Points to Consider (2010) (155)
- Newborn Screening Technology: Proceed With Caution (2006) (141)
- Children, Families, and Health Care Decision Making (1999) (139)
- Relational Autonomy: Moving Beyond the Limits of Isolated Individualism (2014) (138)
- Human Subjects Protections in Community-Engaged Research: A Research Ethics Framework (2010) (125)
- Gender Differences in the Authorship of Original Research in Pediatric Journals, 2001–2016 (2017) (117)
- Research Ethics Education for Community-Engaged Research: A Review and Research Agenda (2012) (108)
- Ethical issues in increasing living kidney donations by expanding kidney paired exchange programs. (2000) (101)
- Implications of disclosing individual results of clinical research. (2006) (99)
- Addressing the Ethical Challenges in Genetic Testing and Sequencing of Children (2014) (94)
- From genetics to genomics: ethics, policy, and parental decision-making. (2009) (92)
- Parental attitudes regarding newborn screening of PKU and DMD (2003) (92)
- Lethal language, lethal decisions. (2003) (92)
- Children as Hematopoietic Stem Cell Donors (2010) (92)
- PRIMUM NON NOCERE: AVOIDING HARM TO VULNERABLE WAIT LIST CANDIDATES IN AN INDIRECT KIDNEY EXCHANGE (2001) (91)
- Mandatory extended searches in all genome sequencing: "incidental findings," patient autonomy, and shared decision making. (2013) (83)
- Maternal-Fetal Intervention and Fetal Care Centers (2011) (82)
- A pilot study to explore knowledge, attitudes, and beliefs about sickle cell trait and disease. (2009) (80)
- Biobank participation and returning research results: Perspectives from a deliberative engagement in South Side Chicago (2012) (80)
- Health care decisionmaking by children. Is it in their best interest? (1997) (78)
- Ethical issues in genetic testing of children. (2000) (78)
- Screening for conditions that do not meet the Wilson and Jungner criteria: The case of Duchenne muscular dystrophy (2006) (77)
- Privacy, Intimacy and Isolation (1993) (72)
- Should We Mandate a COVID-19 Vaccine for Children? (2020) (70)
- Predictive Genetic Testing for Conditions that Present in Childhood (2002) (65)
- Against the Tide: Arguments against Respecting a Minor's Refusal of Efficacious Life-Saving Treatment (2009) (65)
- Consent for Emergency Medical Services for Children and Adolescents (2011) (62)
- Ethical issues in identifying and recruiting participants for familial genetic research (2004) (61)
- Mandatory versus Voluntary Consent for Newborn Screening? (2010) (61)
- The OHRP and SUPPORT. (2013) (61)
- Newborn screening for cystic fibrosis: a lesson in public health disparities. (2008) (59)
- Should all living donors be treated equally? (2002) (57)
- Parental Attitudes and Beliefs regarding the Genetic Testing of Children (2005) (54)
- Empirical data about women's attitudes towards a hypothetical pediatric biobank (2008) (54)
- Ethics and Professionalism in the Pediatric Curriculum: A Survey of Pediatric Program Directors (2009) (53)
- Paediatricians' attitudes and practices towards HPV vaccination (2008) (52)
- Ethical considerations related to pregnancy in transplant recipients. (2006) (51)
- Are minority children under- or overrepresented in pediatric research? (2003) (49)
- Newborn screening for lysosomal storage diseases: an ethical and policy analysis (2012) (49)
- Reporting Incidental Findings in Genomic Scale Clinical Sequencing-A Clinical Laboratory Perspective: A Report of the Association for Molecular Pathology. (2015) (48)
- Effect of family history on disclosure patterns of cystic fibrosis carrier status (2003) (48)
- Are doctors altruistic? (2002) (47)
- Incorporating newborn screening into prenatal care. (2004) (47)
- Pediatricians' Attitudes Toward Expanding Newborn Screening (2005) (46)
- Disclosing misattributed paternity. (1996) (46)
- Physician Refusal to Provide Information or Treatment on the Basis of Claims of Conscience (2009) (45)
- Risk, prognosis, and unintended consequences in kidney allocation. (2011) (43)
- Immunisation against chickenpox (1995) (43)
- Do Genetic Relationships Create Moral Obligations in Organ Transplantation? (2002) (42)
- Minimizing risks: the ethics of predictive diabetes mellitus screening research in newborns. (2003) (42)
- Incidental findings of therapeutic misconception in biobank-based research (2012) (42)
- Genetic Exceptionalism vs. Paradigm Shift: Lessons from HIV (2001) (41)
- Ethical assessment of clinical asthma trials including children subjects. (2004) (41)
- Minors as Living Solid-Organ Donors (2008) (40)
- Saving lives is more important than abstract moral concerns: financial incentives should be used to increase organ donation. (2009) (40)
- Children in Medical Research (2006) (40)
- Methodology matters. (2007) (40)
- Engaging African-Americans about biobanks and the return of research results (2012) (39)
- Do healthy children deserve greater protection in medical research? (2003) (38)
- Disclosing the Diagnosis of HIV in Pediatrics (2001) (38)
- Phase I research and the meaning of direct benefit. (2006) (38)
- Racial disparities in reaching the renal transplant waitlist: is geography as important as race? (2015) (38)
- Are research ethics standards satisfied in pediatric journal publications? (2002) (38)
- Reactions of pediatricians to refusals of medical treatment for minors. (2010) (37)
- Ethics of placebos in clinical asthma trials. (2006) (37)
- Overriding a patient's refusal of treatment after an iatrogenic complication. (1997) (36)
- Attitudes of African-American parents about biobank participation and return of results for themselves and their children (2012) (36)
- Practical and Ethical Challenges to Paired Exchange Programs (2004) (35)
- American Academy of Pediatrics policy statements on bioethics: summaries and commentaries: part 1. (2008) (35)
- Equal Opportunity Supplemented by Fair Innings: Equity and Efficiency in Allocating Deceased Donor Kidneys (2012) (35)
- And a Time to Die: How American Hospitals Shape the End of Life (2006) (35)
- Empirical data about women's attitudes toward a biobank focused on pregnancy outcomes (2008) (34)
- Maternal knowledge and attitudes about newborn screening for sickle cell disease and cystic fibrosis (2009) (34)
- Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq (2019) (34)
- Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children (2006) (33)
- Children in Medical Research: Access versus Protection (2006) (33)
- A Historical and Current Review of Newborn Screening for Neuromuscular Disorders From Around the World: Lessons for the United States. (2017) (32)
- Attitudes and Counseling Practices of Pediatricians Regarding Youth Sports Participation and Concussion Risks (2017) (32)
- Spinal Muscular Atrophy: Past, Present, and Future. (2019) (31)
- Defining Death: The Case for Choice (2016) (31)
- Religious Exemptions to the Immunization Statutes: Balancing Public Health and Religious Freedom (1997) (31)
- Professional and personal attitudes about access and confidentiality in the genetic testing of children: a pilot study. (2003) (30)
- Nine Key Functions for a Human Subjects Protection Program for Community-Engaged Research: Points to Consider (2010) (30)
- Universal state newborn screening programs can reduce health disparities. (2015) (30)
- Fragile X screening: Attitudes of genetic health professionals (2009) (30)
- In defense of a single standard of research risk for all children. (2005) (29)
- SARS-CoV-2 vaccine testing and trials in the pediatric population: biologic, ethical, research, and implementation challenges (2021) (29)
- Age and equity in liver transplantation: An organ allocation model (2015) (29)
- Parental Understanding of Newborn Screening for Cystic Fibrosis After a Negative Sweat-Test (2011) (28)
- Heterozygote Carrier Testing in High Schools Abroad: What are the Lessons for the U.S.? (2006) (27)
- Adolescent Sexuality and Public Policy: A Liberal Response (1996) (27)
- The Ethical Limits in Expanding Living Donor Transplantation (2006) (27)
- Introducing Genetic Tests With Uncertain Implications in Living Donor Kidney Transplantation (2016) (26)
- Restricting Living-Donor–Cadaver-Donor Exchanges to Ensure that Standard Blood Type O Wait-List Candidates Benefit (2004) (26)
- Paired exchanges should be part of the solution to ABO incompatibility in living donor kidney transplantation. (1998) (26)
- Teaching and assessment of ethics and professionalism: a survey of pediatric program directors. (2013) (26)
- Pediatric Resident Preparedness and Educational Experiences With Informed Consent. (2016) (25)
- Solid Organ Donation between Strangers (2002) (25)
- Pediatrician-Family-Patient Relationships: Managing the Boundaries (2009) (25)
- Children in Medical Research: balancing protection and access: has the pendulum swung too far? (2004) (25)
- Better than Best (Interest Standard) in Pediatric Decision Making (2019) (25)
- What the Medical Excuse Teaches Us About the Potential Living Donor as Patient (2010) (25)
- Achieving Justice in Genomic Translation: Re-Thinking the Pathway to Benefit (2012) (24)
- Ethical and policy issues in pediatric genetics (2008) (23)
- Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology. (2015) (23)
- Impact of the kidney allocation system on young pediatric recipients (2018) (23)
- Decision making in liver transplantation—Limited application of the liver donor risk index (2014) (22)
- Attitudes of healthcare professionals and parents regarding genetic testing for violent traits in childhood (2004) (22)
- Kidney Donor Profile Index Does Not Accurately Predict the Graft Survival of Pediatric Deceased Donor Kidneys (2016) (22)
- Media Appeals for Directed Altruistic Living Liver Donations: Lessons from Camilo Sandoval Ewen (2002) (21)
- Shared decision making in deceased-donor transplantation (2006) (21)
- The Role of Gender in Publication in The Journal of Pediatrics 2015‐2016: Equal Reviews, Unequal Opportunities (2018) (21)
- Association of Transplant Center With Survival Benefit Among Adults Undergoing Heart Transplant in the United States. (2019) (20)
- Theory and Practice of Pediatric Bioethics (2016) (20)
- Does Familiarity Breed Acceptance? The Influence of Policy on Physicians' Attitudes Toward Newborn Screening Programs (2006) (20)
- Good Ethics Requires Good Science: Why Transplant Programs Should NOT Disclose Misattributed Parentage (2010) (19)
- Predictive Genetic Testing of Children and the Role of the Best Interest Standard: Currents in Contemporary Bioethics (2013) (18)
- The participation of minorities in published pediatric research. (2005) (18)
- In Defense of the Hopkins Lead Abatement Studies (2002) (17)
- Why “Doctor, if this Were your Child, What Would You Do?” Deserves an Answer (2003) (17)
- The Advantages and Challenges of Testing Children for Heritable Predisposition to Cancer. (2016) (17)
- Policy considerations in designing a fragile X population screening program (2008) (17)
- Reopening Schools Safely: The Case for Collaboration, Constructive Disruption of Pre-Coronavirus 2019 Expectations, and Creative Solutions (2020) (17)
- Reopening K-12 Schools in the Era of Coronavirus Disease 2019: Review of State-Level Guidance Addressing Equity Concerns (2020) (16)
- 360 Degrees of Human Subjects Protections in Community-Engaged Research (2010) (16)
- When physicians forego the doctor–patient relationship, should they elect to self-prescribe or curbside? An empirical and ethical analysis (2009) (16)
- A re‐examination of the use of ethnicity in prenatal carrier testing (2012) (16)
- Moral Grounding for the Participation of Children as Organ Donors (1993) (16)
- Pediatric Professionals' Attitudes about Secondary Findings in Genomic Sequencing of Children. (2015) (16)
- A Compounding of Errors: The Case of Bone Marrow Donation between Non-Intimate Siblings (2006) (15)
- Parents: critical stakeholders in expanding newborn screening. (2012) (15)
- Should Medical Errors Be Disclosed to Pediatric Patients? Pediatricians' Attitudes Toward Error Disclosure. (2016) (15)
- The ethics of preadoption genetic testing. (2001) (15)
- Hypoplastic left heart syndrome: a paradigm case for examining conscientious objection in pediatric practice. (2009) (15)
- Pediatric research and the federal minimal risk standard. (2006) (14)
- Ethics of hematopoietic stem cell transplantation in type 1 diabetes mellitus. (2007) (14)
- Religion, conscience, and controversial clinical practices. (2007) (14)
- First World Consensus Conference on pancreas transplantation: Part II – recommendations (2021) (14)
- Ethics and professionalism in medical physics: a survey of AAPM members. (2013) (14)
- Whether and why pediatric researchers report race and ethnicity. (2003) (13)
- Relational Autonomy as the Key to Effective Behavioral Change (2013) (13)
- Ethical issues in pediatric trials. (2001) (13)
- Ethical and Logistical Issues Raised by the Advanced Donation Program "Pay It Forward" Scheme. (2017) (12)
- Impact of the Coronavirus Disease 2019 Pandemic on Authorship Gender in The Journal of Pediatrics: Disproportionate Productivity by International Male Researchers (2020) (12)
- The Ethics of Type 1 Diabetes Prediction and Prevention Research (2003) (12)
- Certificates of confidentiality in research: rationale and usage. (2004) (12)
- Justice for children: the child as organ donor. (1994) (12)
- Attitudes and Beliefs of Sports Medicine Providers to Sickle Cell Trait Screening of Student Athletes (2011) (12)
- Convening a 407 Panel for Research Not Otherwise Approvable: "Precursors to Diabetes in Japanese American Youth" as a Case Study (2004) (12)
- What Is Wrong with the Physician Charter on Professionalism (2006) (12)
- Donating a Second Kidney: A Tale of Family and Ethics (2000) (12)
- The Moral Status of the Newborn and its Implications for Medical Decision Making (2007) (12)
- Informed consent for genetic research involving pleiotropic genes: an empirical study of ApoE research. (2006) (11)
- An Empirical Investigation of Physicians’ Attitudes Toward Intrasibling Kidney Donation by Minor Twins (2008) (11)
- All Donations Should Not Be Treated Equally: A Response to Jeffrey Kahn's Commentary (2002) (11)
- In defense of the American Academy of Pediatrics Policy Statement—Children as Hematopoietic Stem Cell Donors (2011) (11)
- American Academy of Pediatrics policy statements on bioethics: summaries and commentaries: part 2. (2008) (11)
- Attitudes and beliefs of pediatricians and genetic counselors regarding testing and screening for CF and G6PD: Implications for policy (2006) (11)
- Communicating with parents about immunization safety: messages for pediatricians in the IOM report "the childhood immunization schedule and safety: stakeholder concerns, scientific evidence, and future studies". (2013) (10)
- Qualitative insights into how pediatric pay-for-performance programs are being designed. (2009) (10)
- Kidney exchange programs: an expanded view of the ethical issues (1998) (10)
- Developing an ethics framework for living donor transplantation (2018) (10)
- A pilot study to evaluate knowledge and attitudes of Illinois pediatricians toward newborn screening for sickle cell disease and cystic fibrosis. (2011) (10)
- Ethical Issues in Dialysis Alan Spital, Series Editor: Do Not Resuscitate Orders and Iatrogenic Arrest During Dialysis: Should “No” Mean “No”? (2003) (10)
- Arguments against health care autonomy for minors. (1995) (10)
- An ethical and policy analysis of elective transplantation for metabolic conditions diagnosed by newborn screening. (2010) (10)
- Sickle Cell Trait Screening in Athletes: Pediatricians' Attitudes and Concerns (2011) (10)
- Ethical and policy issues in newborn screening of children for neurologic and developmental disorders. (2015) (10)
- Living Kidney Donors Who Develop Kidney Failure: Excerpts of Their Thoughts (2016) (10)
- Pediatricians are More Supportive of the Human Papillomavirus Vaccine than the General Public (2008) (10)
- Patient Confidentiality and the Surrogate's Right to Know (2000) (10)
- Premature guidance about whole-genome sequencing. (2013) (10)
- Human subject protections in genetic research. (2004) (10)
- Young physicians' recall about pediatric training in ethics and professionalism and its practical utility. (2013) (10)
- Maternal attitudes about sickle cell trait identification in themselves and their infants. (2010) (10)
- Prisoners as Living Donors: A Vulnerabilities Analysis (2017) (9)
- The Best Interest Standard: Same Name but Different Roles in Pediatric Bioethics and Child Rights Frameworks (2017) (9)
- The case against COVID‐19 vaccine mandates in pediatric solid organ transplantation (2022) (9)
- Ethical Analysis and Policy Recommendations Regarding Domino Liver Transplantation (2018) (9)
- American academy of pediatrics policy statements on bioethics: summaries and commentaries: part 3. (2008) (8)
- Age Should Not Be Considered in the Allocation of Deceased Donor Kidneys (2012) (8)
- Ethical and policy issues in genetic testing. (2001) (8)
- Disclosing Health and Health Behavior Information between Living Donors and Their Recipients. (2015) (8)
- Living kidney donors and ESRD. (2015) (8)
- It is time to revise the kidney allocation system to restore the pediatric advantage (2018) (8)
- Minority Children in Pediatric Research (2003) (8)
- Newborn screening for sickle cell disease: whose reproductive benefit? (2011) (8)
- Respecting Choice in Definitions of Death. (2018) (8)
- The Advantages and Challenges of Testing Children for Heritable Predisposition to Cancer. (2016) (8)
- We Need a Registry of Living Kidney Donors (2007) (8)
- The ethics of hematopoietic stem cell donation by minors. (2009) (7)
- Revise the Uniform Determination of Death Act to Align the Law With Practice Through Neurorespiratory Criteria (2022) (7)
- Identification and management of sickle cell trait by young physicians. (2012) (7)
- Public Attitudes and Knowledge About Youth Sports Participation and Concussion Risk in an Urban Area. (2018) (7)
- The Challenges of Incorporating Research Ethics Consultation Into Institutional Human Subjects Protections Programs (2018) (7)
- How Different Conceptions of Risk Are Used in the Organ Market Debate (2010) (7)
- Life support for patients with cervical-level quadriplegia. (1993) (7)
- Should doctors reconstruct the vaginal introitus of adolescent girls to mimic the virginal state? Surgery is not what it seems. (1998) (7)
- Genetic testing of adolescents: is it in their best interest? (2000) (7)
- Should children and adolescents undergo genetic testing? (2004) (7)
- A Descriptive and Moral Evaluation of Providing Informal Medical Care to One’s Own Children (2009) (7)
- Reflections on Charlie Gard and the Best Interests Standard From Both Sides of the Atlantic Ocean. (2020) (7)
- Forty Years Later: The Scope of Bioethics Revisited (2010) (6)
- Ethical issues in pediatric genetics (2006) (6)
- Informed Consent in Pediatric Research (2004) (6)
- Are we ready to expand donation after cardiac death to the newborn population? (2011) (6)
- Different Standards Are Not Double Standards: All Elective Surgical Patients Are Not Alike (2012) (6)
- Adolescent autonomy in health care? (2003) (6)
- Potential inefficiency of a proposed efficiency model for kidney allocation. (2008) (6)
- Growth attenuation by commission and omission may be ethically justifiable in children with profound disabilities. (2007) (6)
- Newborns and other children: in defense of differential attitudes and treatment. (2013) (5)
- Baby at Risk: The Uncertain Legacies of Medical Miracles for Babies, Families, and Society (2007) (5)
- Speciation (review) (2005) (5)
- Ethical and Policy Issues in Newborn Screening: Historical, Current, and Future Developments (2009) (5)
- Pediatricians' attitudes toward resuscitation in children with chronic illnesses (2009) (5)
- A pilot study to evaluate awareness of and attitudes about prenatal and neonatal genetic testing in postpartum African American women. (2013) (5)
- Pediatric Decision Making Requires Both Guidance and Intervention Principles (2018) (5)
- Lessons to be learned from the 407 process. (2005) (5)
- Arguments against Respecting a Minor's Refusal of Efficacious Life-Saving Treatment Redux, Part II (2009) (4)
- Payment in Pediatric Research (2006) (4)
- Against newborn screening for type 1 diabetes. (2007) (4)
- Gender and race/ethnicity differences in living kidney donor demographics: Preference or disparity? (2021) (4)
- To tell or not to tell: attitudes of transplant surgeons and transplant nephrologists regarding the disclosure of recipient information to living kidney donors (2015) (4)
- Commentary: Surgery is not what it seems (1998) (4)
- The Ethics of Organ Transplantation in Persons with Intellectual Disability by Lainie Friedman Ross, MD, PhD. (2021) (4)
- The Use of Race, Ethnicity, and Social Determinants of Health in Three Pediatrics Journals. (2022) (4)
- In Reply: ABO‐Incompatible List‐Paired Exchanges Including an O Recipient Cannot be Ethically Justified (2006) (4)
- Diversity, Equity, and Inclusion in The Journal of Pediatrics. (2021) (4)
- COVID-19 Vaccine Refusal and Organ Transplantation (2022) (4)
- Responding to the Challenge of the Children's Health Act: An Introduction to Children in Research (2003) (4)
- Immunisation against chickenpox: Authors’ reply. (1995) (4)
- Genetic Testing of Children: Who Should Consent? (2008) (4)
- Consent Is the Cornerstone of Ethically Valid Research: Ethical Issues in Recontacting Subjects Who Enrolled in Research as a Minor (2015) (4)
- Genetic Testing by Sports Medicine Physicians in the United States: Attitudes, Experiences, and Knowledge (2018) (4)
- Pediatricians’ Attitudes About Screening Newborns for Infectious Diseases (2010) (4)
- The Moral and Legal Need to Disclose Despite a Certificate of Confidentiality (2014) (4)
- Adding Another Voice to the Living Donor Kidney Transplant Discussions at the CIBA Symposium of 1966 (2016) (3)
- Protect NIH's DNA advisory committee (2018) (3)
- A pilot study to determine whether health care professionals perceive stigma in heterozygote carrier identification and disclosure decisions (2011) (3)
- Abusive Head Trauma and Parental Participation in Pediatric Decision Making (2020) (3)
- Surrogate Decision Making for Children: Who Should Decide? (2019) (3)
- The safety dance (2015) (3)
- Unspoken ambivalence in kinship obligation in living donation (2018) (3)
- From Detached Concern to Empathy: Humanizing Medical Practice (review) (2003) (3)
- Carrier detection in childhood: a need for policy reform (2010) (2)
- All living donors should not be treated equally (2003) (2)
- In Further Defense of “Better than Best (Interest)” (2019) (2)
- In further defense of the American Academy of Pediatrics Committee on Bioethics “children as hematopoietic stem cell donors” statement (2011) (2)
- Black Women and Babies Matter (2021) (2)
- Salmeterol and inhaled corticosteroids in patients with persistent asthma. (2001) (2)
- The Need for Consistency in 407 Reviews (2004) (2)
- Prenatal Testing and Disability Rights (review) (2002) (2)
- Pediatric Intensivist and Pediatric Neurologist Perspectives and Practices on Death by Neurologic Criteria (2021) (2)
- Clinical and ethical considerations in managing carrier detection. (2009) (2)
- Ethical Issues Raised by the Media Portrayal of Adolescent Transplant Refusals. (2020) (2)
- The Living Organ Donor as Patient (2021) (2)
- Simulation of Ventilator Allocation Strategies During the COVID-19 Pandemic (2020) (2)
- Engaging African-Americans about biobanks and the return of research results (2012) (2)
- Just Caring@@@Women & Children in Health Care: An Unequal Majority (1995) (2)
- (Women and) children first: applicable to lifeboats? Applicable to human experimentation? (2002) (2)
- Patient Autonomy: Imperfect, Insufficient, but Still Quite Necessary (2002) (2)
- Ethics of Organ Transplantation in Persons with Intellectual Disability (2021) (2)
- DO PEER GUIDELINES OR EDITORIAL POLICIES AFFECT THE REPORTING AND DISCUSSION OF RACE AND ETHNICITY IN PEDIATRIC RESEARCH? (2005) (2)
- The Pediatrician’s Moral Obligation to Counsel Directively Against Youth Tackle Football (2020) (2)
- The University of Chicago Institute for Translational Medicine (2009) (1)
- Attitudes of Lay Stakeholders and Transplant Professionals About Disclosure to Living Kidney Donors in Exchanges and Chains (2016) (1)
- Outcomes after kidney donation. (2014) (1)
- 50 Years Ago in The Journal of Pediatrics: Editorial Comment: Therapeutic Orphans. (2018) (1)
- The 1966 Ciba Symposium on Transplantation Ethics: 50 Years Later. (2016) (1)
- More Discussion about Misattributed Parentage in Transplantation (2011) (1)
- Missed Opportunities in the Preparticipation Physical Examination for High School Athletes (2019) (1)
- The Dead Donor Rule Does Require that the Donor is Dead (2023) (1)
- The participation of children in nontherapeutic diabetes research in the US (2007) (1)
- Benchmarks of Fairness for Health Care Reform By Norman Daniels, Donald W. Light, and Ronald L. Caplan (review) (2015) (1)
- My sibling’s keeper: What are the ethical issues surrounding participation of minors as hematopoietic stem cell donors? (2010) (1)
- Phase I Research and the Meaning of ‘Prospect of Direct Benefit’ (2006) (1)
- Prospective Psychosocial Monitoring of Living Kidney Donors Using the SF-36 Health Survey. (2003) (1)
- Are we adequately protecting vulnerable patients in longitudinal observational studies? (2011) (1)
- Ethical and Policy Issues in Genetic Testing (2001) (1)
- The Ambivalence That Cannot Be Spoken: Kinship Obligation in Living Kidney Donation (2018) (1)
- Race in the Reading: A Study of Problematic Uses of Race and Ethnicity in a Prominent Pediatrics Textbook (2022) (1)
- Patient, Heal Thyself: How the New Medicine Puts the Patient in Charge (2009) (1)
- 9 Research in Schools (2006) (1)
- 50 Years Ago in The Journal of Pediatrics: Maternal Phenylketonuria: Implications for Growth and Development. (2018) (1)
- 50 Years Ago in The Journal of Pediatrics: Variability in the Manifestations of Phenylketonuria/Transient Hyperphenylalaninemia. (2018) (1)
- Ethical and policy lessons to be learned from a family with inherited bone marrow failure (2008) (1)
- 50 years ago in the Journal of Pediatrics: mass screening for phenylketonuria. (2012) (1)
- An Ethical Analysis of Newborn Congenital Cytomegalovirus Screening. (2022) (1)
- The Ethical Limits of Children's Participation in Clinical Research. (2020) (1)
- African-Americans with End Stage Renal Disease in the Early Years of Kidney Transplantation. (2019) (1)
- Living Donation by Individuals with Life-Limiting Conditions (2019) (1)
- Newborn Screening for Krabbe Disease: What Illinois Can Learn from New York (2013) (1)
- 50 Years Ago in TheJournal ofPediatrics: Evaluation of the Effects of Terminating the Diet in Phenylketonuria. (2016) (1)
- Long-term consequences of kidney donation. (2009) (1)
- The Complexities of Ascertaining Public Preferences for Newborn Screening Policies. (2018) (1)
- International Pediatric Transplant Association (IPTA) position statement supporting prioritizing pediatric recipients for deceased donor organ allocation (2022) (1)
- 50 Years Ago in The Journal of Pediatrics: Plus ça Change: Halfway Technologies in Pediatrics. (2020) (1)
- Newborn screening for conditions that do not meet the Wilson and Jungner criteria. (2009) (1)
- Evolution of the 407 Process (2006) (1)
- Consent for clinical research. (1997) (1)
- Why Most Bad Decisions About Vaccines Do Not Constitute Child Neglect. (2020) (1)
- Is It Appropriate to Attenuate Growth in Profoundly Developmentally Disabled Children to Facilitate Their Care (2007) (1)
- "Medical Benefit" and Therapeutic Misconception: The Ethical Conundrum of Phase 1 Pediatric Oncology Research. (2021) (1)
- A Non-Paternalistic Conception of Relational Autonomy Still Needs Others (2013) (1)
- Should a PVS patient be a live organ donor? (2006) (1)
- The Need to Promote All Pediatric Stem Cell Donors’ Understanding and Interests (2014) (1)
- Should We Provide Healthy Children with Greater Protection in Medical Research (2006) (1)
- Ethical and Legal Issues for the Primary Care Physician (2008) (0)
- Human Subject Protections in Pediatric Research (2006) (0)
- SU-E-E-03: Ethics and Professionalism Education in Medical Physics: A Needs Assessment Study. (2012) (0)
- Child maltreatment and modifying factors in Shanghai, China. (2019) (0)
- Health Care Surrogacy Laws Do Not Adequately Address the Needs of Minors. (2020) (0)
- Contributors (1977) (0)
- Coding the Dead: Cardiopulmonary Resuscitation for Organ Preservation. (2023) (0)
- Delegating Decision-Making Authority To a Surrogate. (2019) (0)
- Clinical Ethics in Pediatrics: Genetic testing and screening of minors (2011) (0)
- Clarifying the Blurry Boundaries between Research and Clinical Care (2022) (0)
- When, If Ever, Is It Ethical to Do Research in Developing Countries That Could Not Be Done Ethically in Developed Countries? (2018) (0)
- Restricted Role of the Liver Donor Risk Index in Shared Decision-Making.: Abstract# B1106 (2014) (0)
- When is it ethical for a minor to serve as a living organ donor? (2008) (0)
- 42: ASSOCIATION BETWEEN STUDY FACTORS AND ENROLLMENT BY RACE/ETHNICITY IN PEDIATRIC ACUTE CARE RESEARCH (2021) (0)
- Limits to Confidentiality: Ethical Issues in End-of-Life Care (2012) (0)
- 50 Years Ago in TheJournalofPediatrics: Renal Homotransplantations in Children. (2020) (0)
- Chapter 260 – Ethical and Legal Issues in Pediatrics (2005) (0)
- Essay Review Forty Years Later (2010) (0)
- Expanding living kidney donation: ethical and policy considerations (2013) (0)
- Presymptomatic Testing for Genetic Disease: Ethical Considerations.• 155 (1997) (0)
- Against newborn screening for type 1 diabetes. Author's reply (2007) (0)
- 50 Years Ago in T he J ournal of P ediatrics Public He (2022) (0)
- 419: PRACTICES AND PERSPECTIVES IN PEDIATRIC DETERMINATION OF DEATH BY NEUROLOGIC CRITERIA (2020) (0)
- 50 years ago in the Journal of Pediatrics: identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses. (2012) (0)
- 50 Years Ago in TheJournalofPediatrics: Attention-Deficit/Hyperactivity Disorder Contextualized. (2021) (0)
- 50 Years Ago in TheJournalofPediatrics: Points to Consider: Sickle Cell Screening. (2022) (0)
- Inherited Susceptibility to Cancer: Clinical, Predictive, and Ethical Perspectives (review) (2000) (0)
- 49: ARE RACIAL/ETHNIC MINORITIES OVER- OR UNDERREPRESENTED IN RESEARCH ENROLLING SERIOUSLY ILL CHILDREN? (2020) (0)
- PRACTICES ABOUT DO NOT ATTEMPT RESUSCITATION ARE INFLUENCED BY WHAT PHYSICIANS WOULD WANT FOR THEIR OWN CHILDREN AND NOT BY THEIR SUBSPECIALTY AFFILIATION.: 524 (2006) (0)
- Diabetes Prediction and Prevention Research in Childhood (2006) (0)
- The Cambridge Textbook of Bioethics: Prenatal testing and newborn screening (2008) (0)
- Describing how children with life threatening complex chronic conditions die. (2018) (0)
- Book Review Transplanting Human Tissue: Ethics, Policy, and Practice Edited by Stuart J. Youngner, Martha W. Anderson, and Renie Schapiro. 216 pp. New York, Oxford University Press, 2004. $42.50. 0-19-516284-6 (2004) (0)
- Correspondence on “Exploring the motivations of research participants who chose not to learn medically actionable secondary findings about themselves” by Schupmann et al (2021) (0)
- Should living organ donors receive financial incentives (2009) (0)
- Contents Vol. 43, 2016 (2016) (0)
- Living Kidney Donors and Their Recipients: Who Wants to Know What?: Abstract# A327 (2014) (0)
- 50 Years Ago in TheJournalofPediatrics: Shifting Attitudes toward the Disclosure of Serious Illness. (2020) (0)
- Measuring high-risk parents' opinions about direct-to-consumer genetic testing for adult-onset inherited cancer syndromes in their adolescent and young adult children. (2023) (0)
- Lead Abatement Research (2006) (0)
- Protecting research subjects. (2002) (0)
- Refusals of the Determination of Death by Neurologic Criteria: A Mixed Methods Study of Physician Perspectives on Refusals Cases. (2023) (0)
- Reflections on Ethics and Advocacy in Child Health (REACH): Creating a Forum for Ethical Dialogue (2021) (0)
- 50 Years Ago in TheJournal ofPediatrics: Parents of the Mentally Retarded Child: Emotionally Overwhelmed or Informationally Deprived? (2019) (0)
- Useful Bodies: Humans in the Service of Medical Science in the Twentieth Century (review) (2005) (0)
- The Rare and Atypical Diabetes Network (RADIANT) Study: Design and Early Results. (2023) (0)
- Minors as Living Solid-Organ Donors (Clinical Report) (2013) (0)
- Mandatory Coronavirus Disease 2019 Vaccine for Children?-Reply. (2021) (0)
- Chapter 60 – Ethics in Living Donor Transplantation (2015) (0)
- Clinical Asthma Trials (2006) (0)
- Children as Living Donors (2016) (0)
- Engaging family stakeholders in post-discharge NICU missions. (2019) (0)
- Transplantation Ethics (review) (2001) (0)
- Pediatric Bioethics: Newborn Screening (2009) (0)
- Is kidney donation in the donor's best interest? (2003) (0)
- When Do Family Members Have a Right to Know Genetic Information About a Patient (2007) (0)
- The Harms of Carrier Status Identification: A Cautionary Warning Against Newborn Sequencing. (2020) (0)
- M1890 Is There a Justification for the Attitudes and Practices of Hepatologists and Transplant Surgeons Regarding Transplantation in Patients with Alcoholic Liver Disease (2008) (0)
- 50 Years Ago in The Journal of Pediatrics: Phenylketonuria in a Negro Infant. (2015) (0)
- 531: Sociodemographic Characteristics and Reasons for Refusals of Determination of Brain Death (2020) (0)
- Research not Otherwise Approvable: A Look at One 407 Protocol (2006) (0)
- Expounding on Shared Decision Making in Pediatrics. (2022) (0)
- The Ethics of Hematopoletic Stem Cell Donation by Minors. Authors' reply (2009) (0)
- Public health and criminal justice are intertwined (2020) (0)
- 50 Years Ago in T J P (2018) (0)
- American Academy of Pediatrics Policy Statements on Bioethics (2008) (0)
- Analyzing Trends in the Global Surge of Coronavirus Disease 2019 Pandemic Submissions to The Journal of Pediatrics (2021) (0)
- Behavioral Genetics: The Clash of Culture and Biology (review) (2001) (0)
- 50 Years Ago in TheJournal ofPediatrics: Why Patients Don't Follow Medical Advice: A Study of Children on Long-Term Antistreptococcal Prophylaxis. (2019) (0)
- Impact of KDPI On Shared Decision-Making.: Abstract# C1867 (2014) (0)
- Is academic medicine for sale? (2000) (0)
- 50 years ago in the Journal of Pediatrics: comparison of serum phenylalanine levels with growth in Guthrie's inhibition assay in newborn infants. (2012) (0)
- Threading the Needle for the Tiniest Babies. (2017) (0)
- 50 Years Ago in TheJournal ofPediatrics: Legislation and Advances in Medical Knowledge-Acceleration or Inhibition? (2016) (0)
- The philosopher as partner: an introduction to the scholarship of Robert M. Veatch (2022) (0)
- State Versus Adolescent Override for Parental Refusals to Vaccinate Against COVID-19. (2022) (0)
- Minimizing Risks: Diabetes Research in Newborns (2006) (0)
- Response: Adolescent Sexuality and Public Policy: An Unrepentant Liberal Approach (1996) (0)
- Diagnosis, treatment and disclosure: A qualitative exploration of participant challenges in a Monogenic Diabetes Registry. (2023) (0)
- From 1966 to 2005: Balancing Protection and Access in Pediatric Research (2006) (0)
- From Lyon to Louisville: the need for tolerance (2000) (0)
- A festschrift in memory of Robert M. Veatch (2022) (0)
- T1205 A Systematic Review and Ethical Assessment of Clinical Trials in Ulcerative Colitis (2009) (0)
- Access versus Protection: Minority Representation in Pediatric Research (2006) (0)
- Overview of the Common Rule and Subpart D (2006) (0)
- Type 1 Diabetes Mellitus Ethics of Hematopoietic Stem Cell Transplantation in (2008) (0)
- 50 Years Ago in The Journal of Pediatrics: Conference on Treatment of Phenylketonuria. (2017) (0)
- The Journal of Pediatrics Turns 90! A Perspective on Progress, Opportunities, and Challenges. (2022) (0)
- The Role of Ethics and Ethicists in International Case Studies: A Reflective Equilibrium Approach (2014) (0)
- 50 Years Ago in TheJournal ofPediatrics: A New Diagnostic Test for Hemoglobin S. (2020) (0)
- Engaging family stakeholders in post-discharge NICU missions. (2019) (0)
- My sibling’s keeper (2010) (0)
- Pediatric bioethics: reintroducing the parents. (1999) (0)
- Is it reasonable to demand reasons in pediatric decision making? (2022) (0)
- Subject Index Vol. 1, 2001 (2001) (0)
- Authors' reply (1995) (0)
- 50 Years Ago in The Journal of Pediatrics: Prenatal Detection of Genetic Defects. (2019) (0)
- Ethical and policy issues raised by heterozygote carrier identification and predictive genetic testing of adolescents. (2011) (0)
- Book Reviews-Children, Families, and Health Care Decision-Making (2000) (0)
- Genetics and Ethics in the Newborn: The Future is Now H2013: Joint Program: Section on Bioethics and Section on Perinatal Pediatrics (2015) (0)
- Contents Vol. 1, 2001 (2001) (0)
- The editor-in-chief and associate editors wish to express their gratitude to the following individuals who have graciously accepted responsibility for review- ing manuscripts for issues of Community Genetics. (2015) (0)
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