Neil A. Hanchard

ORCID: 0000-0003-1925-2665

Also affiliated with Baylor College of Medicine, University of California System, National Human Genome Research Institute

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 27 papers. Top paper: “SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia”.

SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia

Brain(2023)10.1093/brain/awac460

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0.992DataRank · unranked

35 citations

Hagar Mor Shaked, Kenneth Gable, Sita D. Gupta, Xueyang Pan, Niranjanakumari Somashekarappa +93 more

High-depth African genomes inform human migration and health

Nature(2020)10.1038/s41586-020-2859-7

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0DataRank · unranked

370 citations

Shaun Aron, Laura R. Botigué, Dhriti Sengupta, Gerrit Botha, Taoufik Bensellak +62 more

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

Genetics in Medicine(2020)10.1038/s41436-020-01027-3

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0DataRank · unranked

49 citations

Kirsty McWalter, Heleen te Brinke, Lodewijk IJlst, Petra M. Mooijer, Jos P.N. Ruiter +95 more

Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

Genetics in Medicine(2020)10.1038/s41436-020-00984-z

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0DataRank · unranked

42 citations

Cecilia Esteves, Anna Bican, Rebecca C. Spillmann, Heidi Cope, Allyn McConkie‐Rosell +89 more

COPB2 haploinsufficiency causes a coatopathy with osteoporosis and developmental delay

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.09.14.297234

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0DataRank · unranked

1 citations

Lindsay C. Burrage, Aurélie Clément, Bernardo Blanco‐Sánchez, Rossella Venditti, Mahim Jain +49 more

Pressure-Mediated Reflection Spectroscopy Criterion Validity as a Biomarker of Fruit and Vegetable Intake: A 2-Site Cross-Sectional Study of 4 Racial or Ethnic Groups

Journal of Nutrition(2021)10.1093/jn/nxab349

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0DataRank · unranked

41 citations

Nancy E. Moran, Qiang Wu, Lisa Harnack, Neal E. Craft, Neil A. Hanchard +7 more

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8

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0DataRank · unranked

49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 more

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.002

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0DataRank · unranked

41 citations

Lindsay C. Burrage, Rossella Venditti, Aurélie Clément, Bernardo Blanco‐Sánchez, Mahim Jain +48 more

Unmapped exome reads implicate a role for Anelloviridae in childhood HIV-1 long-term non-progression

npj Genomic Medicine(2021)10.1038/s41525-021-00185-w

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0DataRank · unranked

7 citations

Lesedi Williams, Gaone Retshabile, Eric Katagirya, Gerald Mboowa, Busisiwe Mlotshwa +26 more

“Iron”ing out hemophagocytosis through PIEZO1

Cell(2021)10.1016/j.cell.2021.01.038

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0DataRank · unranked

6 citations

Ambroise Wonkam, Neil A. Hanchard

A dominant negative variant of RAB5B disrupts maturation of surfactant protein B and surfactant protein C

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2105228119

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0DataRank · unranked

31 citations

Jiehong Pan, David R. Spielberg, Neil A. Hanchard, Daryl A. Scott, Lindsay C. Burrage +21 more

Five Priorities of African Genomics Research: The Next Frontier

Annual Review of Genomics and Human Genetics(2022)10.1146/annurev-genom-111521-102452

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0DataRank · unranked

31 citations

Nchangwi Syntia Munung, Collet Dandara, Kevin Esoh, Neil A. Hanchard, Guida Landouré +1 more

Promoting Pharmacogenomics in Africa: Perspectives From Variation in G6PD and Other Pharmacogenes

Clinical Pharmacology & Therapeutics(2022)10.1002/cpt.2816

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0DataRank · unranked

9 citations

Houcemeddine Othman, Ananyo Choudhury, David Twesigomwe, Neil A. Hanchard, Blessing R. Sitabule

Tailored community engagement to address the genetics diversity gap

Med(2022)10.1016/j.medj.2022.05.010

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0DataRank · unranked

4 citations

Maria H. Chahrour, Jantina de Vries, Neil A. Hanchard

Genetics for all: Tri-directional research engagement as an equitable framework for international partnerships

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100140

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0DataRank · unranked

0 citations

Toluwani Taiwo, Neil A. Hanchard, Thalia Billawala

Long-term non-progression and risk factors for disease progression among children living with HIV in Botswana and Uganda: A retrospective cohort study

International Journal of Infectious Diseases(2023)10.1016/j.ijid.2023.11.030

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0DataRank · unranked

6 citations

Grace P. Kisitu, Savannah Mwesigwa, John Farirai, Eric Katagirya, Gaone Retshabile +28 more

RAB1A haploinsufficiency phenocopies the 2p14–p15 microdeletion and is associated with impaired neuronal differentiation

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.009

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0DataRank · unranked

4 citations

Yang Li, Nandina Paria, Ryan J. Bohlender, Chad Huff, Jill A. Rosenfeld +17 more

Killer cell immunoglobulin receptor diversity and its relevance in the human host’s response to HIV infection in African populations

Translational Medicine Communications(2023)10.1186/s41231-023-00141-z

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0DataRank · unranked

2 citations

Marion Amujal, Obondo James Sande, Moses Joloba, Daudi Jjingo, David Patrick Kateete +5 more

A first-generation genome-wide map of correlated DNA methylation demonstrates highly coordinated and tissue-independent clustering across regulatory regions

Research Square(2023)10.21203/rs.3.rs-2852818/v1

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0DataRank · unranked

4 citations

Owen Hirschi, Katharina Schulze, Yongtao Guan, Neil A. Hanchard, Aarti Jajoo

Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome

medRxiv(2023)10.1101/2023.09.20.23295800

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0DataRank · unranked

1 citations

Katharina Schulze, Ian E. Copeland, Manasa Atyam, Kendra Kamp, Neil A. Hanchard +5 more

Identification of a Clade-Specific HLA-C*03:02-Restricted Epitope GY9 Derived from the HIV-1 p17 Matrix Protein

Preprints.org(2023)10.20944/preprints202310.0441.v1

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0DataRank · unranked

1 citations

Savannah Mwesigwa, Gyaviira Nkurunungi, Gaone Retshabile, Moses Egesa, Joel Kabali +20 more

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations

Bioinformatics(2024)10.1093/bioinformatics/btae148

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0DataRank · unranked

16 citations

Stephanie M. Gogarten, Joohyun Kim, Xing Hua, Julie‐Alexia Dias, Quan Sun +89 more

Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension

JCI Insight(2024)10.1172/jci.insight.172152

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4 citations

Edmond Wonkam‐Tingang, Monesha Gupta‐Malhotra, S. Shahrukh Hashmi, Yixing Han, Aarti Jajoo +19 more

Common and rare genetic variation intersects with ancestry to influence human skin and plasma carotenoid concentrations

medRxiv(2024)10.1101/2024.12.20.24319465

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0DataRank · unranked

0 citations

Savannah Mwesigwa, Qiang Wu, Melissa N. Laska, Stephanie Jilcott Pitts, Nancy E. Moran +2 more

Aberrant One-Carbon Metabolism and Ancestral Genetics Underlie Edematous Severe Acute Malnutrition

Research Square(2025)10.21203/rs.3.rs-6890799/v1

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0DataRank · unranked

0 citations

Natasha Lie, Yixing Han, Qing Li, Aarti Jajoo, J.D. Redmond +22 more

Transcriptome-directed analysis for Mendelian disease diagnosis overcomes limitations of conventional genomic testing

Journal of Clinical Investigation(2020)10.1172/jci141500

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0DataRank · unranked

189 citations

Hongzheng Dai, Lindsay C. Burrage, Jill A. Rosenfeld, Shamika Ketkar, Michaela Müller +13 more

Pathway-Specific Polygenic Risk Scores for Blood Pressure Traits in a West African Cohort

medRxiv(2025)10.1101/2025.06.30.25330577

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0DataRank · unranked

0 citations

Vanessa Robbin, Tinashe Chikowore, Yuji Zhang, Ananyo Choudhury, Scott Hazelhurst +5 more