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75 years of The American Journal of Human Genetics

American journal of human genetics, 2024-01, Vol.111 (1), p.1-2

Korf, Bruce R.

2024

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Describing human populations: An evolving picture in human genetics research

American journal of human genetics, 2021-12, Vol.108 (12), p.2207-2207

Korf, Bruce R

2021

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Recognizing those who deal with rare disease every day

American journal of human genetics, 2021-02, Vol.108 (2), p.213-213

Korf, Bruce R.

2021

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

Genetics in medicine, 2017-02, Vol.19 (2), p.249-255

2017

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Neurofibromatosis type 1

Journal of the American Academy of Dermatology, 2009-07, Vol.61 (1), p.1-14

2009

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ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

Genetics in medicine, 2013-07, Vol.15 (7), p.565-574

2013

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New approaches to molecular diagnosis

JAMA : the journal of the American Medical Association, 2013-04, Vol.309 (14), p.1511

2013

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Celebrating excellence, acknowledging past harms: Both are vital parts of ASHG’s continuing journey to advance human genetics

American journal of human genetics, 2023-03, Vol.110 (3), p.371-372

2023

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Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2018-07, Vol.20 (7), p.671-682

2018

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Neurofibromatosis

Handbook of Clinical Neurology, 2013, Vol.111, p.333-340

Korf, Bruce R.

2013

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Neurofibromatosis type 1

Nature reviews. Disease primers, 2017-02, Vol.3 (1), p.17004-17004, Article 17004

2017

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The American Journal of Human Genetics Welcomes Human Genetics and Genomics Advances to the ASHG Publications Family

American journal of human genetics, 2020-06, Vol.106 (6), p.727-728

2020

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Pathophysiology of neurofibromatosis type 1

Annals of internal medicine, 2006-06, Vol.144 (11), p.842

2006

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Pitfalls and challenges in genetic test interpretation: An exploration of genetic professionals experience with interpretation of results

Clinical genetics, 2021-05, Vol.99 (5), p.638-649

2021

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Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic Ancestry Groups in Biomedical Publications

JAMA : the journal of the American Medical Association, 2024-04, Vol.331 (15), p.1276

2024

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Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics

Genetics in medicine, 2014-11, Vol.16 (11), p.804-809

2014

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Neurofibromatosis type 1 revisited

Pediatrics (Evanston), 2009-01, Vol.123 (1), p.124

2009

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Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

Nature genetics, 2024-04, Vol.56 (4), p.555-556

2024

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Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

American journal of human genetics, 2024-04, Vol.111 (4), p.621-623

2024

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Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing

PLoS genetics, 2015-11, Vol.11 (11), p.e1005637-e1005637

2015

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An Update on Neurofibromatosis Type 1-Associated Gliomas

Cancers, 2020-01, Vol.12 (1), p.114

2020

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Spinal neurofibromatosis and phenotypic heterogeneity in NF1

Clinical genetics, 2015-05, Vol.87 (5), p.399-400

Korf, Bruce R.

2015

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Malignancy in Neurofibromatosis Type 1

The oncologist (Dayton, Ohio), 2000-12, Vol.5 (6), p.477-485

Korf, Bruce R.

2000

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Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics: Hematologic, Renal, and Immunologic Disorders

Seventh edition, 2022

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75 years of The American Journal of Human Genetics

Describing human populations: An evolving picture in human genetics research

Recognizing those who deal with rare disease every day

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

Neurofibromatosis type 1

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

New approaches to molecular diagnosis

Celebrating excellence, acknowledging past harms: Both are vital parts of ASHG’s continuing journey to advance human genetics

Care of adults with neurofibromatosis type 1: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

Neurofibromatosis

Neurofibromatosis type 1

Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas

The American Journal of Human Genetics Welcomes Human Genetics and Genomics Advances to the ASHG Publications Family

Pathophysiology of neurofibromatosis type 1

Pitfalls and challenges in genetic test interpretation: An exploration of genetic professionals experience with interpretation of results

Guidance on Use of Race, Ethnicity, and Geographic Origin as Proxies for Genetic Ancestry Groups in Biomedical Publications

Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics

Neurofibromatosis type 1 revisited

Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

Guidance on use of race, ethnicity, and geographic origin as proxies for genetic ancestry groups in biomedical publications

Mosaic and Intronic Mutations in TSC1/TSC2 Explain the Majority of TSC Patients with No Mutation Identified by Conventional Testing

An Update on Neurofibromatosis Type 1-Associated Gliomas

Spinal neurofibromatosis and phenotypic heterogeneity in NF1

Malignancy in Neurofibromatosis Type 1

Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics: Hematologic, Renal, and Immunologic Disorders

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